Category: Uncategorized

  • Cardiff Oncology Reports First Quarter 2025 Results and Provides Business Update

    – Completed enrollment in randomized Phase 2 CRDF-004 trial evaluating onvansertib + standard of care for the treatment of first-line RAS-mutated metastatic colorectal cancer (“mCRC”) –

    – Expanded intellectual property portfolio with second patent covering treatment of all bev-naïve patients, including RAS-mutated and RAS wild-type mCRC, across all lines of therapy –

    – Cash and investments of $79.9 million as of March 31, 2025, projected runway into Q1 2027 –

    SAN DIEGO, May 08, 2025 (GLOBE NEWSWIRE) — Cardiff Oncology, Inc. (Nasdaq: CRDF), a clinical-stage biotechnology company leveraging PLK1 inhibition to develop novel therapies across a range of cancers, today announced financial results for the first quarter ended March 31, 2025, and provided a business update.

    “Our lead program for onvansertib has remained on track in 2025 with the successful completion of enrollment in our trial in first-line RAS-mutated mCRC, underscoring our deep commitment to serving a patient population that has seen no therapeutic advancements in decades,” said Mark Erlander, Chief Executive Officer of Cardiff Oncology. “Furthermore, we expanded our intellectual property portfolio through the issuance of a second patent covering all mCRC, regardless of tumor mutational status, across all lines of therapy. As we continue to generate clinical data and move toward regulatory discussions with the FDA, we remain focused on our mission to deliver a transformative therapy that could redefine the standard of care for RAS-mutated mCRC and for other cancers.”

    Upcoming expected milestones

    Additional clinical data from the ongoing CRDF-004 trial in mCRC expected in 1H 2025

    Company highlights for the quarter ended March 31, 2025, and subsequent weeks include:

  • early cancer diagnosis

    Early cancer diagnosis is a crucial factor in improving treatment outcomes and survival rates. Detecting cancer at an early stage allows for more effective and less invasive treatments, significantly increasing the chances of successful recovery. With advances in medical technology and artificial intelligence (AI), new tools are emerging to help individuals stay vigilant about their health and take proactive steps towards cancer prevention and early detection.

    One such innovative solution is OncoPreventer, an AI-powered assistant designed to support cancer prevention and early diagnosis. This intelligent health companion offers personalized screening plans, timely reminders, and expert-backed recommendations, all consolidated into a user-friendly app or messenger platform. OncoPreventer leverages cutting-edge AI technology and medical expertise to tailor cancer prevention strategies to each individual's unique characteristics such as age, gender, family history, and lifestyle.

    ### Personalized Screening for Better Outcomes
    Traditional cancer screening schedules can sometimes be generic and do not consider individual risk factors comprehensively. OncoPreventer addresses this gap by creating custom screening plans that are specifically aligned with each user's health profile. By considering factors like genetic predisposition, personal habits, and existing medical conditions, the app ensures that users receive the right screenings at the right times, significantly enhancing early cancer detection opportunities.

    ### Smart Reminders for Consistent Monitoring
    One of the challenges in cancer prevention is keeping up with regular check-ups, lab tests, and annual health visits. OncoPreventer resolves this by sending intelligent, timely reminders. These prompts help users stay on track without feeling overwhelmed or stressed, promoting consistent health monitoring and early identification of potential issues.

    ### Trusted Information and Support
    Navigating health information can often be confusing due to complex medical terminology. OncoPreventer simplifies this by providing clear, reliable answers to health-related questions. Users can engage with the AI assistant to understand their condition better, get advice on preventive measures, and stay informed without the hassle of medical jargon or misinformation.

    ### Progress Tracking and Engagement
    Understanding health progress is key to motivation and adherence to prevention plans. OncoPreventer offers interactive timelines and health summaries, enabling users to visualize their screening history, upcoming appointments, and achieved milestones. This feature fosters a sense of control and encourages proactive engagement in one's health journey.

    ### Seamless Multi-Platform Access
    Recognizing the diversity in technology preferences, OncoPreventer is accessible across web browsers, Telegram, and WhatsApp. This seamless integration ensures users can interact with their health companion anytime, anywhere, making cancer prevention convenient and adaptable to their daily routines.

    ### The Value of OncoPreventer in Early Cancer Diagnosis
    Early cancer diagnosis fundamentally transforms the approach to cancer care, shifting from reactive treatment to proactive prevention. OncoPreventer embodies this shift by placing personalized, expert-driven support at users' fingertips. Its AI capabilities enhance the accuracy of risk assessment and the timeliness of interventions, crucial elements in catching cancer early or preventing it altogether.

    By combining technology with a compassionate, easy-to-use interface, OncoPreventer not only helps reduce cancer risk but also alleviates the anxiety associated with health management. It empowers individuals to take control in a manageable, informed way, ultimately contributing to better health outcomes and peace of mind.

    ### Conclusion
    The fight against cancer begins with awareness and early action. Tools like OncoPreventer exemplify how AI and personalized medicine can revolutionize cancer prevention and early diagnosis. By providing tailored screening schedules, smart reminders, trusted health advice, and progress tracking, OncoPreventer is more than just an app—it is a true partner in proactive, preventative care.

    Incorporating OncoPreventer into your health routine means staying informed, prepared, and ahead in the battle against cancer. It is an investment in your health that leverages the power of AI to protect your future with personalized, hassle-free care. Take charge today and make early cancer diagnosis a cornerstone of your health strategy with OncoPreventer—the intelligent health companion designed just for you.

  • Opinion: Social Support is Key to Endometrial Cancer Survivor Recovery

    Oncology nurses provide care at every stage of the cancer journey, from diagnosis to survivorship. While the end of active treatment often brings relief, the transition to survivorship can present new challenges for patients, including uncertainty, lingering physical symptoms, and emotional stress.

    By understanding these how social support and physician-patient communication impact quality of life (QOL), oncology nurses can better guide patients through this often stressful transition, ultimately improving QOL.

    Impact of Social Support on Patients with Endometrial Cancer

    Mandato et al. explored the influence of social support and physician-patient communication on QOL and emotional well-being in patients with endometrial cancer during the first year post surgery. The study examined how social support from family, friends, and significant others and communication quality with healthcare providers affected patients’ recovery.

    The study included 127 patients, 98 of whom returned completed questionnaires at 1 month and/or 1 year post surgery. The Short Form-36 and Multidimensional Scale of Perceived Social Support were used to evaluate emotional well-being and social support, respectively. Clinical factors such as comorbidities, body mass index (BMI), cancer grade, type of surgery, and adjuvant therapies were analyzed in relation to QOL scores.

    Patients reporting high social support 1 month after surgery had significantly higher emotional well-being at both 1 month and 1 year post surgery (P < .05). High perceived social support 1 year post surgery was associated with better general health scores (P < .05). Family support was linked to higher social functioning scores at 1 month and fewer emotional limitations at 1 year (P < .05).

    Support from significant others at 1 year was associated with improved physical functioning (P < .005), reduced pain (P < .05), less fatigue (P < .05), and better general and emotional well-being (P < .05). Additionally, higher social support levels were correlated with fewer medical visits during the year post surgery.

    Conversely, patients with comorbidities, such as hypertension and diabetes, reported higher levels of overall pain 1 year after surgery. Those with a BMI above the median exhibited lower physical functioning and general health scores at 1 year. Patients with grade 3 endometrial cancer had lower social functioning scores compared to those with grade 2 endometrial cancer, while those with grade 2 endometrial cancer had higher general health scores compared to grade 1 endometrial cancer.

    Furthermore, patients who underwent minimally invasive laparoscopy but were converted to laparotomy, a more invasive open surgery, and those with longer surgery durations, reported lower physical function scores at 1 year. Conversely, longer hospital stays were associated with higher general health scores, and postoperative complications correlated with higher energy/fatigue scores.

    Patients who received brachytherapy alone had better physical role functioning 1 month post surgery compared to those who received both brachytherapy and external beam radiation therapy.

    Regarding communication during diagnosis, 59.8% of patients had a family member present. The majority (75.3%) received their diagnosis in a gynecological oncology clinic, and 85.6% felt that the time allotted for communication was adequate. Most patients (82.5%) found physician communication to be empathetic and supportive, and 91.8% felt their privacy was protected.

    Nursing Considerations

    Patients with longer hospital stays, often associated with more severe conditions or complications, surprisingly reported higher general health scores 1 year after surgery. This may reflect a sense of resilience or improved well-being following recovery from more serious health challenges. Additionally, patients who experienced postoperative complications reported higher energy/fatigue scores, indicating that, despite setbacks, they felt more energetic and vital. These findings suggest that overcoming significant health hurdles may foster a greater sense of vitality and general health in the long term.

    This study underscores the vital role of social support and physician-patient communication in improving the QOL and emotional well-being of endometrial cancer patients. Those who felt supported by family, friends, and significant others reported better physical, social, and emotional functioning in the months following surgery.

    For oncology nurses, these findings highlight the importance of fostering open, empathetic communication with patients. Dedicating time to discussing diagnosis, treatment options, and postoperative care, and involving family members when appropriate, can enhance the support system crucial to patient well-being.

    References

    Mandato VD, Paterlini M, Torricelli F, Rabitti E, Mastrofilippo V, Aguzzoli L. Perceived social support and quality of life in endometrial cancer patients: a longitudinal study. Front Oncol. 2024;14:1447644. Published 2024 Aug 2. doi:10.3389/fonc.2024.1447644

  • Protagonist Therapeutics, Inc. (PTGX): Among the Best Cancer Stocks to Invest in for Long-Term Gain

    Artificial intelligence (AI) is revolutionizing numerous industries, and one of the most impactful transformations is happening in the field of oncology — the study and treatment of cancer. As cancer remains a leading cause of mortality worldwide, combining AI technology with oncology has the potential to drastically improve diagnosis accuracy, personalize treatments, and ease the burden on healthcare systems. According to a report by Mordor Intelligence, the AI market in oncology is projected to expand from around $1.98 billion in 2025 to a staggering $9.04 billion by 2030. This impressive growth rate, with a compound annual growth rate (CAGR) of 35.51%, reflects how deeply AI is embedding itself into cancer-related healthcare practices.

    A major reason AI is such a game changer in oncology is its ability to handle immensely complex datasets — something human clinicians struggle with given time constraints and the sheer volume of data. From advanced image recognition algorithms that assist in early tumor detection to personalized medicine models predicting patient responses to specific treatments, AI streamlines workflows and portends better patient outcomes. North America, primarily the U.S., currently dominates this innovative landscape, driven by heavy investment and technological infrastructure. However, the Asia-Pacific region is rapidly catching up, showcasing the globalization of AI in cancer care. These geographic trends reveal immense opportunities for investors eyeing cancer stocks with promising long-term potential, especially those already embraced by savvy hedge funds.

    Delving into the investment angle, a rigorous methodology was applied to pinpoint the top cancer stocks primed for long-term gains. The process began by filtering companies with high 5-year average returns and then cross-referencing this list with hedge fund data from Insider Monkey, focusing on the number of hedge fund holders per stock as of Q4 2024. Hedge funds are institutional investors renowned for their research prowess and selective strategies, so their picks often serve as strong signals for retail investors. The combination of robust past financial performance and hedge fund endorsement offers a compelling lens to evaluate potential market winners — and it’s no coincidence that mimicking hedge fund activity has historically outperformed broader market indexes by significant margins.

    One standout company emerging from this analysis is Protagonist Therapeutics, Inc. (NASDAQ: PTGX), a biopharmaceutical titan making waves with its innovative peptide-based therapies. Unlike conventional drugs, peptides are short chains of amino acids that can selectively modulate complex biological processes. Protagonist’s flagship cancer-related drug, Rusfertide, is in Phase 3 clinical trials targeting polycythemia vera (PV), a blood disorder characterized by excessive red blood cells. Rusfertide mimics the hormone hepcidin to regulate iron metabolism and aims to control hematocrit levels more effectively than traditional methods like phlebotomy, which can be invasive and cause quality-of-life issues. The company’s partnerships with pharmaceutical giants such as Takeda and Johnson & Johnson further bolster its credibility and financial strength, exemplified by upfront and milestone payments totaling hundreds of millions of dollars. Notably, Protagonist has significantly boosted its cash reserves in 2024, signaling strong operational footing.

    Looking ahead, Protagonist Therapeutics is expected to release critical clinical trial data soon, including Phase 3 outcomes for Rusfertide and early 2025 data from trials involving other pipeline candidates targeting immune-mediated diseases like psoriasis and ulcerative colitis. These milestones hold considerable sway over the company’s valuation and growth prospects. Although the company posted a modest net loss in Q3 2024, revenue strides from licensing and partnerships combined with milestone payments swung the overall profitability into positive territory for the year. This pattern reflects a common biotech lifecycle where clinical development phases require upfront investment followed by substantial returns upon trial successes and drug approvals. While Protagonist ranks highly among cancer stocks for long-term investment, the burgeoning AI sector within oncology also presents intriguing alternatives. Intriguingly, some AI stocks that began 2025 on a strong note have outperformed more established cancer stocks, suggesting diversification into AI-driven healthcare could yield robust returns.

    Beyond the immediate investment pointers, it’s fascinating to reflect on how AI's role in cancer care is reshaping the entire ecosystem. For example, AI algorithms today can analyze thousands of pathology slides in minutes, achieving diagnostic accuracy comparable to expert oncologists. Some AI platforms even integrate genomic data and patients’ electronic health records, enabling truly personalized treatment plans that predict therapeutic response and minimize adverse effects. Furthermore, hospitals are deploying AI-powered tools to optimize resource allocation, such as predicting patient inflows to efficiently manage chemotherapy suites and equipment. The synergy between AI and oncology is expected to accelerate as machine learning models grow more sophisticated and more extensive datasets become available. This ongoing convergence is not only a beacon of hope for millions of patients worldwide but also an exciting frontier for investors and innovators alike.

    #CancerStocks #ArtificialIntelligence #OncologyInnovation #BiotechInvesting #HealthcareAI #ProtagonistTherapeutics #TechInMedicine

  • Cancer Patients Often Do Better with Less Intensive Treatment, New Research Finds

    Recent studies presented at the American Society of Clinical Oncology conference have brought promising news for patients suffering from ovarian and esophageal cancer as well as Hodgkin lymphoma. These studies indicate that less intensive treatment approaches may be just as effective as more aggressive regimens, all while reducing the risk of complications and improving patient quality of life. One standout study conducted by French researchers focused on ovarian cancer patients undergoing surgery. Traditionally, the removal of lymph nodes during ovarian cancer surgery has been a common procedure intended to prevent the spread of cancer. However, this study showed that avoiding the removal of healthy lymph nodes did not negatively impact survival rates over a period of nine years. Furthermore, the avoidance of unnecessary lymph node removal significantly decreased the incidence of complications related to the surgery. This finding challenges the conventional wisdom and highlights the potential benefits of less invasive surgical techniques. In another important study carried out in Germany, researchers examined treatment options for esophageal cancer, a disease known for its aggressive nature and poor prognosis. Patients in this study either received chemotherapy followed by surgery alone or chemotherapy and surgery along with radiation therapy. After a rigorous comparison, the findings revealed no statistically significant difference in three-year survival rates between the two groups. This suggests that the addition of radiation may not always be necessary, thereby sparing patients the added side effects and stress that accompany radiation treatment. The third study addressed the treatment of advanced Hodgkin lymphoma. Traditionally, intense chemotherapy regimens have been used to combat this cancer, but these treatments often come with substantial toxicities that can diminish patients' quality of life. The German-led research discovered that a gentler chemotherapy regimen not only produced better outcomes at the four-year mark but also resulted in fewer side effects compared to the more aggressive treatment. This could signify a major shift in how oncologists manage Hodgkin lymphoma, favoring approaches that balance efficacy with tolerability. Collectively, these studies embody a growing trend in oncology: moving towards personalized, optimal cancer care that emphasizes doing enough to effectively treat the disease but avoids the harms of overtreatment. This philosophy is centered on the understanding that more aggressive treatment does not always equate to better outcomes and that patient well-being extends beyond survival statistics to encompass quality of life during and after therapy. The implications of these findings are significant. They suggest that cancer treatment protocols may need reevaluation, with a stronger focus on minimizing unnecessary interventions. This could lead to shorter hospital stays, reduced healthcare costs, fewer treatment-related complications, and an overall improvement in patient experiences. Cancer patients often endure a multitude of physical and emotional challenges during their treatment journeys. Reducing treatment intensity without compromising effectiveness has the potential to alleviate much of this burden. For example, sparing healthy lymph nodes from removal during ovarian cancer surgery can reduce the risk of lymphedema—a painful and chronic swelling condition. Patients who avoid additional radiation in esophageal cancer treatment can escape radiation-associated side effects such as fatigue, skin problems, and esophageal inflammation. Similarly, gentler chemotherapy protocols for Hodgkin lymphoma can help prevent long-term toxicities including heart and lung problems. Oncologists and medical professionals are embracing these findings as they work to tailor treatments to individual patient needs, balancing the scales between efficacy and safety. These studies exemplify the careful and methodical research necessary to challenge established standards and innovate patient care. As with any medical advancements, it is essential for patients to consult their healthcare providers to understand how these findings might apply to their specific cases. Cancer treatment remains highly individualized, and decisions must take into account tumor characteristics, overall health, patient preferences, and other critical factors. In conclusion, the research unveiled at the American Society of Clinical Oncology conference underscores an important paradigm shift in cancer treatment. By demonstrating that less intensive therapeutic approaches may yield similar survival outcomes with reduced side effects, these studies pave the way for treatments that prioritize patient well-being alongside clinical effectiveness. This optimistic outlook offers hope for improved cancer care in the years to come, reshaping the future of oncology towards smarter, gentler, and more compassionate therapies.

  • Experimental Immunotherapy Shows Promise in Bladder Cancer Treatment

    In a groundbreaking development for bladder cancer treatment, an experimental immunotherapy drug named cretostimogene has demonstrated promising results, offering new hope for patients whose cancers have stopped responding to existing therapies. These encouraging findings were shared during the Society of Urologic Oncology meeting in Dallas, marking a significant milestone in the fight against this often stubborn and aggressive cancer. Bladder cancer, particularly in its advanced stages, can be notoriously difficult to treat once it becomes resistant to chemotherapy, immunotherapy, and other targeted treatments. The introduction of cretostimogene could signal a new era of hope, improving outcomes for patients who previously had limited options.

    The late-stage clinical trial featured 112 patients who had advanced bladder cancer resistant to standard therapies. These patients represent a particularly challenging group, as their disease had progressed despite multiple attempts at treatment. What makes the trial results especially encouraging is that the administration of cretostimogene was largely manageable, with most participants avoiding invasive procedures or hospitalization during their treatment period. This indicates a favorable safety profile, which is a crucial consideration in oncology where treatment side effects can sometimes be as daunting as the disease itself. Dr. Mark Tyson, the study’s lead investigator, highlighted that the drug works by effectively activating the patient’s immune system to target and combat bladder cancer cells. This mechanism of action taps into the body’s natural defenses, a strategy that is increasingly transforming cancer therapy worldwide.

    Cretostimogene is not just a hopeful experimental drug; it has already secured regulatory authorization for continued clinical trials and is under evaluation for broader approval based on its demonstrated efficacy and safety. Ambaw Belay, President of CG Oncology—the biotech company behind cretostimogene—expressed cautious optimism about the drug’s future. The trial data not only support further clinical development but also suggest that cretostimogene may soon become an integral part of the standard treatment regimen for patients battling advanced bladder cancer. Such a transition would mark one of the most significant advances in bladder cancer therapy in recent years, reflecting how innovative immunotherapies are reshaping oncology.

    Bladder cancer treatments have long faced the hurdle of tumor resistance, making the introduction of a new agent like cretostimogene a beacon of progress. Resistance to treatments such as chemotherapy and previous immunotherapies can leave patients with dwindling options and a poor prognosis. This new drug’s ability to stimulate an immune response against resistant cancer cells not only holds potential for improved survival but also enhances the quality of life for those affected. Future research aims to build on these findings by enrolling larger patient populations to validate safety and effectiveness on a broader scale. Additionally, there are plans to explore combination therapies that could further boost the drug’s therapeutic impact, potentially leading to longer-lasting remissions or even cures.

    The presentation of these findings at the Society of Urologic Oncology meeting underscores the ongoing commitment within the medical community to combat bladder cancer through innovative research. It highlights how immunotherapy, a field that has revolutionized the treatment of multiple cancers such as melanoma and lung cancer, continues to evolve and expand into new territories. Drugs like cretostimogene represent the frontier of personalized cancer care, tailored to harness the body’s immune system with precision and power. As development continues, this novel approach promises to transform the prognosis for many bladder cancer patients, turning a once formidable diagnosis into a challenge increasingly within the realm of control and hope.

    #BladderCancer #Immunotherapy #Cretostimogene #CancerResearch #OncologyInnovation #HealthcareBreakthroughs #PersonalizedMedicine

  • From Bench to Bedside: SHRO-Led Review Illuminates the Translational Power of Liquid Biopsy in Gynecological Oncology | Newswise

    Newswise — Philadelphia, PA – 08 May 2025 – A landmark review, now published in the Journal of Experimental & Clinical Cancer Research, offers a sweeping and authoritative synthesis on the use of liquid biopsy in gynecological oncology placing this emerging tool at the forefront of precision medicine for women. Led by Professor Antonio Giordano, President of the Sbarro Health Research Organization (SHRO) and molecular oncologist at Temple University and the University of Siena, the study lays out a rigorous translational roadmap to bridge cutting-edge molecular diagnostics with real-world clinical application.

    The article, titled "Liquid biopsy in gynecological cancers: a translational framework from molecular insights to precision oncology and clinical practice," presents a decisive shift from mere technical exploration to clinically actionable guidance. It systematically addresses how liquid biopsy, through circulating tumor DNA (ctDNA), tumor-educated platelets, microRNAs, and extracellular vesicles, can revolutionize the diagnosis, monitoring, and therapeutic tailoring of endometrial, cervical, and ovarian cancers.

    A Translational Vision

    What distinguishes this review is its explicit focus on translational relevance. It does not limit itself to theoretical or laboratory insights. Rather, it rigorously maps fourteen critical fields of inquiry from assay design and biomarker validation to clinical endpoints and cost-effectiveness with a central aim: enabling reliable, standardized integration of liquid biopsy into routine oncology care.

    The authors argue that liquid biopsy is not merely an innovation in biomarker detection, it is a methodological bridge that aligns molecular biology with patient-centered care. This is especially vital in gynecological cancers, where the heterogeneity of disease and anatomical constraints often hinder early diagnosis and longitudinal monitoring. By offering a noninvasive, repeatable, and dynamic window into tumor biology, liquid biopsy has the potential to transform the clinical management of cancers that impact over 1.3 million women in the United States alone.

    Clinical Impact and Gender Relevance

    The implications for women's health are particularly profound. For ovarian cancer, where early-stage detection remains notoriously difficult, liquid biopsy demonstrates up to 90% specificity and increasing sensitivity through combined microRNA and ctDNA panels. In endometrial cancer, personalized ctDNA analysis shows over 87% concordance with traditional tissue-based classification and can predict recurrence several months in advance of clinical imaging.

    In cervical cancer, circulating HPV DNA and specific serum protein levels such as SCC-Ag and VCAM-1 correlate with prognosis and therapy response, reinforcing the value of plasma-based surveillance. Moreover, ctDNA profiling has proven effective in tracking chemotherapy resistance, especially in BRCA-mutated tumors treated with PARP inhibitors.

    These findings underscore not only the scientific innovation, but the gendered urgency of the work: the application of liquid biopsy in gynecological malignancies is not an abstract advance, but a concrete opportunity to improve survival, reduce diagnostic invasiveness, and individualize treatment for millions of women.

    Overcoming Barriers, Building Integration

    Despite its promise, the authors emphasize that liquid biopsy remains underutilized in clinical gynecologic oncology. The review therefore presents detailed considerations to overcome the barriers that prevent translation from the need for FDA-approved multi-analyte assays to standardization of sample handling and AI-driven data interpretation.

    The article calls for rigorous clinical trials that move beyond biomarker performance in advanced disease, toward validation in early-stage settings and population-level screening. Particular attention is paid to the integration of fragmentomics, methylomics, and machine learning in refining diagnostic precision.

    A Message from SHRO Leadership

    “This work is a testament to the potential of translational science to serve not only innovation, but people,” says Professor Antonio Giordano. “Liquid biopsy offers us the unprecedented ability to detect, understand, and treat cancer in real time without waiting for symptoms to emerge or disease to advance. For gynecological cancers, this may well mean the difference between life and loss.”

    SHRO continues to promote scientific rigor, cross-disciplinary collaboration, and patient-centered innovation as pillars of its research mission. This publication reflects the organization’s commitment to translational oncology as a vehicle for equity, efficiency, and excellence in cancer care.

    *The full review is available open-access at the Journal of Experimental & Clinical Cancer Research. For media inquiries or expert commentary, please contact SHRO at [email protected].

    About Sbarro Health Research Organization (SHRO)

    The Sbarro Health Research Organization conducts groundbreaking research in cancer, diabetes, and cardiovascular disease. Based in Philadelphia, Pennsylvania, on the campus of Temple University, SHRO’s programs train young scientists from around the globe, accelerating the pace of health research and innovation.

  • From Bench to Bedside: SHRO-Led Review Illuminates the Translational Power of Liquid Biopsy in Gynecological Oncology | Newswise

    A groundbreaking review published in the Journal of Experimental & Clinical Cancer Research has placed liquid biopsy at the cutting edge of gynecological oncology, heralding a new era of precision medicine for women. Spearheaded by Professor Antonio Giordano, a distinguished molecular oncologist and President of the Sbarro Health Research Organization (SHRO), the study presents a comprehensive translational framework that connects advanced molecular diagnostics with practical clinical application. By focusing on real-world implementation, this landmark review moves beyond theoretical discussion into actionable guidance for integrating liquid biopsy into the routine care of women facing endometrial, cervical, and ovarian cancers.

    Liquid biopsy, a technique that detects cancer-related molecules in blood and other body fluids, promises to revolutionize the detection, monitoring, and treatment tailoring of gynecological malignancies. The review meticulously explores how circulating tumor DNA (ctDNA), tumor-educated platelets, microRNAs, and extracellular vesicles serve as key biomarkers in this noninvasive approach. Unlike traditional tissue biopsies, liquid biopsy offers a dynamic and repeatable glimpse into tumor biology, which is especially critical for gynecological cancers notorious for diagnostic challenges due to disease heterogeneity and anatomical complexities. This innovation opens doors for earlier diagnoses, more precise treatment adjustments, and better monitoring of disease progression or recurrence—all essential steps toward personalized care for over 1.3 million women in the United States affected by these cancers annually.

    What sets this review apart is its dedicated focus on translational relevance—the crucial bridge between laboratory discoveries and bedside application. Rather than examining liquid biopsy purely as a laboratory technique, the authors outline fourteen pivotal areas spanning assay design, biomarker validation, clinical outcomes, and cost-effectiveness to ensure this promising technology is standardized and reliably integrated into oncology practices. This holistic approach hopes to surmount existing barriers such as regulatory approval processes and variability in sample handling, which currently hinder widespread clinical adoption. Moreover, the incorporation of emerging fields like fragmentomics, methylomics, and machine learning illustrates how cutting-edge computational tools can refine diagnostic accuracy, ultimately enabling smarter, faster, and more personalized therapeutic decisions.

    The clinical impact of liquid biopsy on women's health cannot be overstated. In ovarian cancer, one of the deadliest gynecological cancers due to late diagnosis, the technology achieves up to 90% specificity and an improved sensitivity when using combined microRNA and ctDNA panels, offering hope for earlier intervention. Endometrial cancer patients benefit from personalized ctDNA analyses that align closely with traditional tissue classifications and can predict disease recurrence months before it becomes radiologically visible. Furthermore, in cervical cancer—where human papillomavirus (HPV) plays a central role—monitoring circulating HPV DNA alongside serum proteins like SCC-Ag and VCAM-1 correlates strongly with treatment response and prognosis, supporting plasma-based surveillance programs. Particularly striking is the ability of ctDNA profiling to track chemotherapy resistance in BRCA-mutated ovarian tumors treated with PARP inhibitors, highlighting liquid biopsy’s role in guiding adaptive therapeutic strategies tailored to tumor evolution.

    Despite these advances, the path to clinical integration is not without obstacles. The review underscores the need for multi-analyte FDA-approved assays tailored to gynecological oncology and stresses consistent protocols for sample capture and processing to avoid variability that could compromise results. Additionally, the application of AI-driven data interpretation promises to manage complex biomarker signatures but requires validation and standardization before becoming routine tools in clinical decision-making. Rigorous prospective clinical trials are urgently needed, especially in early disease and population screening settings, to confirm that liquid biopsy’s impressive performance in advanced cancers translates into tangible survival benefits and improved quality of life for patients. The authors advocate for cross-disciplinary collaboration to expedite these efforts, combining expertise in molecular biology, clinical oncology, bioinformatics, and healthcare economics.

    Reflecting on the significance of this work, Professor Antonio Giordano remarked, “Liquid biopsy offers us the unprecedented ability to detect, understand, and treat cancer in real time without waiting for symptoms to emerge or disease to advance. For gynecological cancers, this may well mean the difference between life and loss.” SHRO continues to champion rigorous scientific inquiry and patient-centered innovation, underscoring translational oncology as a vehicle for equitable and effective cancer care. Situated on the Temple University campus in Philadelphia, the Sbarro Health Research Organization remains at the forefront of health research, nurturing young scientists worldwide to accelerate breakthroughs in cancer, diabetes, and cardiovascular disease. This landmark publication not only advances scientific understanding but also ignites hope for millions of women worldwide facing gynecological cancer challenges.

    #LiquidBiopsy #GynecologicalOncology #PrecisionMedicine #WomenInScience #CancerResearch #TranslationalMedicine #SHRO

  • Former HaysMed oncologist opens new practice in western Kansas

    In western Kansas, a notable development is offering fresh hope and convenience to cancer patients and those with blood disorders. Dr. Robert Rodriguez, a seasoned medical oncologist, has launched the Western Kansas Oncology Group alongside advanced practice provider Amanda Volchko. Their new practice, although based in Tribune, serves a vital regional role by extending care to the neighboring communities of Oakley, Tribune, and Goodland. This initiative addresses a critical need, offering both in-person consultations and telemedicine services across all three critical-access hospitals, significantly enhancing accessibility for patients who previously faced long travel times for treatment.

    Dr. Rodriguez brings a wealth of experience and dedication to his practice. A proud alum of the University of Kansas, he earned both his undergraduate and medical degrees there and completed his residency and fellowship at the University of Kansas Medical Center. After nearly a decade at HaysMed, his decision to establish a practice in western Kansas reflects a deep commitment to his roots and the rural communities that shaped him. Notably, Rodriguez was involved in a high-profile legal confrontation with HaysMed over the restrictive noncompete clauses in doctors’ contracts, a dispute that was eventually resolved through confidential mediation. This determined stand underscores his passion for ensuring that patients in western Kansas have direct, local access to expert care—a principle that defines the Western Kansas Oncology Group.

    Amanda Volchko, who partners with Dr. Rodriguez, complements the practice with her own unique journey. Originally from New Jersey, she trained in Philadelphia before a recruiter brought her to the rural town of Hoxie. Her expressed interest in oncology coincided fortuitously with Rodriguez’s vision, making Western Kansas Oncology Group a fitting home for her expertise and compassion. Together, they offer comprehensive services in oncology and hematology, including treating blood cancers and noncancerous conditions like anemia and low platelet counts, often linked to medication effects or aging. This holistic approach caters not just to cancer but to a spectrum of blood-related health issues, providing rural patients with a broad safety net.

    One of the most critical aspects of the practice is its emphasis on reducing the physical, emotional, and financial burden of cancer treatment by bringing care closer to home. Dr. Rodriguez recognizes the intense toll systemic cancer treatments take on patients. He explains that even with the most effective therapies, the process is grueling, making the lengthy commutes to urban centers for care difficult for both patients and their families. By offering local chemotherapy administration, diagnostics, labs, and evaluations through their Ortiz-based practice and satellite services, the team relieves a significant amount of stress. This model not only improves patient comfort but also trims costs, a vital factor since oncology treatments can be prohibitively expensive. As anyone who has cared for a cancer patient can attest, the ability to avoid long trips can mean the difference between sustained hope and exhaustion.

    Dr. Rodriguez’s personal connection to the communities he serves is perhaps what makes this practice especially promising. A native of Goodland, Kansas, and married to a Larned native, he understands firsthand the challenges rural patients face. His gratitude to the communities that nurtured his growth fuels his mission to give back in the most meaningful way possible—by providing expert, compassionate care where it is most urgently needed. The early response has been overwhelmingly positive, with appointment slots filling quickly, particularly at the Oakley clinic, which is booked through July. Dr. Rodriguez’s commitment extends beyond routine care; he personally oversees all treatment plans, assuring patients they have a dedicated advocate at every stage. His vision—to combine top-tier oncology services with the deep comfort of receiving care near home—is now a lived reality. This new chapter in western Kansas healthcare shines a hopeful light for local patients and their families, promising enhanced quality of life and extended time to enjoy it.

    #WesternKansasOncology #CancerCareCloseToHome #RuralHealthcareHeroes #OncologyInnovation #PatientCenteredCare #TelemedicineInRuralAreas #CommunityFocusedMedicine

  • Olema Oncology to Participate in Upcoming Investor Conferences

    Olema Pharmaceuticals, a clinical-stage biopharmaceutical company rooted in innovation and dedicated to revolutionizing breast cancer treatment, has announced its participation in two highly anticipated investor conferences this May 2025. Known for its sharp focus on targeted therapies addressing not just breast cancer but also expanding into other arenas, Olema is drawing significant attention within the oncology and investment communities alike. The company’s involvement in these conferences signals ongoing developments and provides a platform to showcase the progress and potential of its novel therapeutic candidates.

    The first event where Olema will present is the H.C. Wainwright 3rd Annual BioConnect Investor Conference, scheduled for May 20, 2025, at 4:30 p.m. ET in New York City. This conference focuses on bridging the gap between innovative biotech companies and investors through interactive discussions such as fireside chats, which allow for an intimate and informative exchange of insights. Olema’s presence here is strategic, opening channels of communication with investors eager to learn about cutting-edge therapies and the future direction of cancer treatment. Following this, Olema will also participate virtually in the T.D. Cowen 6th Annual Oncology Innovation Summit on May 27, 2025, at 5 p.m. ET. This summit, renowned for its forward-looking approach, provides insights aligned with upcoming major oncology gatherings like ASCO (American Society of Clinical Oncology) and EHA (European Hematology Association), making it a crucial event for unveiling promising innovations.

    A standout highlight in Olema's drug development pipeline is palazestrant (OP-1250), a proprietary, orally available complete estrogen receptor antagonist (CERAN) and a selective estrogen receptor degrader (SERD). This dual-action drug aims to block and degrade ERs that drive many forms of breast cancer, offering hope for more effective and long-lasting treatments. Currently undergoing a Phase 3 clinical trial known as OPERA-01, palazestrant represents a significant advancement in endocrine-driven cancer therapy. What makes palazestrant particularly interesting is its design as an orally available medication. Oral cancer therapies have the advantage of improving patient quality of life compared to intravenous treatments that require hospital visits — a subtle but vital improvement that’s transforming cancer care globally.

    But Olema’s innovation does not stop with palazestrant. The company is also advancing the development of OP-3136, a potent KAT6 inhibitor. KAT6 enzymes have been implicated in cancer cell proliferation and survival, making them a promising target for novel therapies. By inhibiting KAT6, OP-3136 seeks to disrupt key pathways essential for tumor growth and resistance, potentially offering a complementary approach to existing cancer treatments. The biopharmaceutical company has positioned itself within two major hubs of innovation: headquartered in San Francisco, a city famous for its blend of biotech creativity and technological advancement, with operations in Cambridge, Massachusetts—often dubbed the biotech capital of the world. This strategic positioning allows Olema to harness leading-edge research talent and foster partnerships that drive scientific and clinical progress.

    Delving deeper into the science behind Olema Pharmaceuticals, the focus on endocrine-driven cancers taps into a surprisingly complex biological realm. Breast cancer, one of the most common cancers worldwide, often depends on hormones like estrogen to grow. Traditional therapies have aimed to block estrogen’s effects, but cancers can develop resistance over time, challenging treatment efficacy. Olema’s approach combines the use of a CERAN and SERD in palazestrant, which not only antagonizes but also promotes degradation of the estrogen receptor, potentially overcoming resistance mechanisms. This multi-faceted attack increases the likelihood of robust tumor suppression. It’s an exciting frontier, tackling cancer not only by blocking signals but by knocking down the receptors themselves—a concept that's gaining momentum as researchers unravel the nuances of receptor biology and cancer resistance.

    This commitment to innovation and patient outcomes positions Olema as a company to watch in the evolving landscape of breast cancer therapies. The live webcasts and recorded presentations from Olema’s upcoming investor conferences will be made available on their investor relations website, enabling broader access for stakeholders eager to keep pace with their progress. As the public and scientific community alike await the results of ongoing clinical trials such as OPERA-01, Olema’s dynamic approach to oncology exemplifies the best of contemporary biopharmaceutical research—blending cutting-edge science with a clear patient-centric focus. For more information, enthusiasts and investors can visit www.olema.com to explore the company’s pipeline, corporate mission, and the latest news on their quest to transform cancer care.

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