麻豆传媒

• Alternating pazopanib and bevacizumab found superior to pazopanib alone
• Strategy aims to delay onset of resistance to pazopanib
• Study reveals median progression-free survival of 23.3 months

News — BUFFALO, N.Y. — A phase 1/2 clinical trial for patients with metastatic kidney cancer demonstrated that a novel two-agent treatment regimen developed at Roswell Park Comprehensive Cancer Center more than doubled progression-free survival compared with single-agent treatment. , Professor of Oncology and Medicine and Director of Network Clinical Trials at Roswell Park, served as Principal Investigator of the study and delivered the findings of the phase 2 portion in a p today at the European Society for Medical Oncology (ESMO) Congress in Barcelona, Spain.

Patients in the single-arm study had received no prior therapy. During each 10-week treatment cycle, they received pazopanib (brand name Votrient), which is FDA-approved for the treatment of metastatic clear cell renal carcinoma (mccRCC), on days 1-28. Pazopanib works by shutting down vascular endothelial growth factor (VEGF) signaling, which supports the growth of new blood vessels that feed the tumor. An increase in VEGF activity is thought to produce resistance to pazopanib, so the patients also received bevacizumab (brand name Avastin) on days 36-50 during the cycle, to neutralize VEGF in the hope of extending progression-free survival (PFS).

In clinical trials that supported FDA approval of pazopanib for advanced RCC, the median progression-free survival (PFS) was 11.1 months. Median PFS for patients who received the combination therapy was 23.3 months.

Study participants were assigned to groups of various risk levels using the International Metastatic Renal Cell Carcinoma Database (IMDC). “Because immunotherapy options were available to patients in other risk groups, the phase 2 group included more patients in the Favorable Risk category,” explains Dr. George. “The encouraging results suggest that alternating pazopanib with bevacizumab is a promising treatment regimen for renal cell carcinoma patients in the Favorable Risk group.”

Data from the clinical trial showed equal or superior efficacy compared with immunotherapy combinations or sunitinib (brand name Sutent) administered as a single agent, and superior safety compared with immunotherapy combinations, in patients in the IMDC Favorable Risk group.

Earlier results from a phase 1 study to evaluate safety of this combination were presented at the 2019 Genitourinary Cancer Symposium of the American Society of Clinical Oncology (ASCO).

Based on preclinical studies at Roswell Park, enrolled 51 patients and was conducted at five U.S. cancer centers, including Roswell Park, the University of Pittsburgh, the University of Kansas, the Medical College of Wisconsin and Karmanos Cancer Center in Detroit. Prior preclinical research was funded by Roswell Park/the Roswell Park Alliance Foundation, the National Cancer Institute and Novartis.

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From the world’s first chemotherapy research to the PSA prostate cancer biomarker, Roswell Park Comprehensive Cancer Center generates innovations that shape how cancer is detected, treated and prevented worldwide. Driven to eliminate cancer’s grip on humanity, the Roswell Park team of 4,000 makes compassionate, patient-centered cancer care and services accessible across New York State and beyond. Founded in 1898, Roswell Park was among the first three cancer centers nationwide to become a National Cancer Institute-designated comprehensive cancer center and is the only one to hold this designation in Upstate New York. To learn more about and the , visit , call 1-800-ROSWELL (1-800-767-9355) or email [email protected].