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A. Oliver Sartor, MD

A. Oliver Sartor, MD

Dr. Sartor earned his MD from Tulane University School of Medicine in 1982. After training at the University of Pennsylvania and Tulane Medical School, he completed a fellowship at the National Cancer Institute, where he focused on advanced prostate cancer therapies. He held positions at LSU Medical School and LSU Health Sciences Center, directing oncology programs before joining Dana Farber Cancer Institute in 2006. In 2008, he returned to Tulane University as the C. E. and Bernadine Laborde Professor of Cancer Research.

An internationally recognized expert in prostate cancer, Dr. Sartor’s interests have focused broadly on prostate cancer, predominantly in those patients who failed initial therapies. His publications range from genetic studies on prostate cancer to clinical trials involving novel agents. He has been a lead author on two studies pivotal for FDA drug approval in prostate cancer and has been the PI or co-PI on a number of prospective international clinical trials evaluating new therapies for patients with advanced prostate cancer.

Having published over 500 scholarly articles and having served as the past Chairman of the Department of Defense Prostate Integration Panel, Dr. Sartor, in addition to being the C.E. and Bernadine Laborde Professor of Cancer Research in the Departments of Medicine and Urology, is the Medical Oncology Chair of the GU Committee of the NRG, the Assistant Dean for Oncology at Tulane University School of Medicine, the Medical Director of the Tulane Cancer Center, and the Editor-in-Chief of the peer-reviewed journal, Clinical Genitourinary Cancer. In addition, he is currently a member of the NCI Board of Scientific Counselors (Clinical Sciences and Epidemiology).

Disclosures:

Talks by A. Oliver Sartor, MD

Immunotherapy in Metastatic Prostate Cancer

A. Oliver Sartor, MD, highlights immunotherapy and its goal of harnessing and enhancing the body’s immune system to target and eradicate cancer cells. He emphasizes the distinct mechanisms of immunotherapeutic agents compared to traditional treatments, noting their potential to offer durable responses and improved survival outcomes in specific patient populations.
Dr. Sartor reviews sipuleucel-T, the first FDA-approved immunotherapy for metastatic castrate-resistant prostate cancer (mCRPC), and its ability to extend overall survival, despite minimal impact on disease progression markers like PSA levels. He also addresses the role of immune checkpoint inhibitors, such as pembrolizumab, particularly for mCRPC patients with specific biomarkers like microsatellite instability-high (MSI-H) or mismatch repair deficiency (dMMR). He presents data from recent studies showing promising responses in these subsets of patients, highlighting the importance of genetic profiling in identifying candidates for checkpoint inhibition.
Additionally, Dr. Sartor explores emerging immunotherapeutic approaches, including the use of chimeric antigen receptor (CAR) T-cell therapy and novel vaccines targeting prostate-specific antigens. He discusses the ongoing clinical trials evaluating these innovative treatments and their potential to transform the therapeutic landscape of metastatic prostate cancer.

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Metastatic Castrate-Resistant Prostate Cancer: Options and Possible Sequences

Dr. A. Oliver Sartor outlines the available therapeutic options for metastatic castrate-resistant prostate cancer (mCRPC), which include novel hormonal agents, chemotherapy, immunotherapy, and targeted therapies. He addresses androgen receptor signaling inhibitors such as abiraterone acetate and enzalutamide, and the use of chemotherapy agents like docetaxel and cabazitaxel.

Dr. Sartor also addresses the emerging role of immunotherapy in mCRPC, particularly with agents like pembrolizumab for patients with specific genetic mutations or microsatellite instability. Additionally, he discusses the potential of radionuclide therapies, such as radium-223.

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PSMA Radiopharmaceuticals: Update 2023

A. Oliver Sartor, MD of Tulane University School of Medicine, presents on the use of prostate-specific membrane antigen (PSMA) radiopharmaceuticals in the treatment of prostate cancer in 2023. He provides a comprehensive overview of recent advancements, clinical applications, and future directions for PSMA-targeted therapies. He discusses the latest developments in PSMA-based imaging, highlighting the efficacy of PSMA PET/CT scans in detecting prostate cancer metastases with high sensitivity and specificity. Dr. Sartor emphasizes that these imaging techniques have revolutionized the staging and restaging of prostate cancer, enabling more accurate assessment of disease spread and guiding treatment decisions.

Dr. Sartor also covers therapeutic applications of PSMA radiopharmaceuticals, focusing on PSMA-targeted radioligand therapy (RLT). He presents data from recent clinical trials demonstrating the efficacy of PSMA RLT with agents such as lutetium-177 (Lu-177) PSMA-617 in patients with metastatic castration-resistant prostate cancer (mCRPC).

In conclusion, Dr. Sartor highlights the transformative impact of PSMA radiopharmaceuticals on the management of prostate cancer, underscoring the potential of PSMA-targeted radiopharmaceuticals to significantly enhance the detection and treatment of prostate cancer, offering new hope for patients with advanced disease.

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