Updated toxicity data from the ongoing SWOG/NRG 1806 clinical trial, which tests combining chemoradiation therapy with immunotherapy in patients with localized muscle-invasive bladder cancer, reveal no significant safety concerns with the combination.
S/N1806 study team member Sameer G. Jhavar, MD, PhD, of Baylor Scott and White Health, of Temple, Texas, will present a safety report on 213 patients as an oral presentation at the 2022 annual meeting of the American Society for Radiation Oncology (ASTRO) in San Antonio on October 25. Study S/N1806 is supported by the National Cancer Institute (NCI), part of the National Institutes of Health (NIH), jointly led by the SWOG Cancer Research Network and NRG Oncology, and conducted by the NIH-funded National Clinical Trials Network (NCTN).
Patients enrolled to the phase 3 S/N1806 trial have non-metastatic muscle-invasive bladder cancer. All patients on the trial are randomized 1:1 to one of two treatment arms. Patients on both arms are treated with standard trimodality therapy, which combines endoscopic surgery to maximally remove the bladder tumor with chemoradiation therapy. The one half of patients on the investigational arm also receive the immunotherapy drug atezolizumab in combination with the chemoradiation, every three weeks for six months.
The lead author on the report is Parminder Singh, MD, a SWOG investigator at the Mayo Clinic in Phoenix, Arizona.
“This is a randomized phase 3 clinical trial investigating the addition of immunotherapy to bladder-preserving trimodality chemoradiation therapy,” Singh said. “There is no sign of significant toxicity concerns in the investigative arm, which suggests the regimen is safe, and the trial continues to accrue very well. If positive, the trial may lead to improved treatment options for patients with bladder cancer by which they can preserve their bladder.”
Among the 213 patients assessed, 113 received the trimodality therapy plus atezolizumab combination. The remaining 100 patients were randomized to the control arm of trimodality therapy alone.
Overall, 65 of the 113 patients (58 percent) on the atezolizumab arm reported Grade 3 or higher toxicities, compared to 44 of 100 patients (44 percent) on the control arm. Most toxicities were hematological and were not considered to be immune related by the treating physician. However, a number of known immune-related adverse events of atezolizumab were reported at Grade 3 or higher on the investigational arm.
An earlier pre-specified safety analysis of the first 80 patients enrolled to the trial also showed no significant increase in toxicity on the investigational arm as compared to the control arm. The S/N1806 trial continues to accrue well and is expected to reach its enrollment goal of 475 patients within the next two years. It is the largest study investigating bladder-preserving therapy in North America.
S/N1806 was funded by the NIH/NCI through grants CA180888, CA180819, CA180820, CA180821, and CA180868; and supported in part by Genentech, a member of the Roche Group, through a Cooperative Research and Development Agreement with the NCI.
In addition to Singh, the S/N1806 study team included Jason A. Efstathiou, of Harvard; Melissa Plets, of SWOG Statistics and Data Management Center and Fred Hutchinson Cancer Center; Sameer G. Jhavar, of Baylor Scott and White Health; Scott E. Delacroix, Jr., of Gulf South MU-NCORP/East Jefferson General Hospital/Louisiana State University; Abhishek Tripathi, of University of Oklahoma; Amit Gupta, of Cedars Sinai Medical Center; Sean Sachdev, of Department of Radiation Oncology, Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine; Ashesh Jani, of Department of Radiation Oncology, Winship Cancer Institute of Emory University; Austin Kirschner, of Department of Radiation Oncology, Vanderbilt University Medical Center; Catherine Tangen, of SWOG Statistics and Data Management Center and Fred Hutchinson Cancer Center; Richard C. Bangs, of Bladder Cancer Advocacy Network; Monika Joshi, of Penn State Cancer Institute; Brian A. Costello, of Division of Medical Oncology, Mayo Clinic, Rochester; Felix Y. Feng, of Helen Diller Family Comprehensive Cancer Center, University of California at San Francisco; Daniel P. Petrylak, of Yale School of Medicine; Ian M. Thompson, Jr., of CHRISTUS Santa Rosa Health System of San Antonio; and Seth P. Lerner, of Baylor College of Medicine, Houston, Texas.
SWOG Cancer Research Network is part of the National Cancer Institute’s National Clinical Trials Network and the NCI Community Oncology Research Program and is part of the oldest and largest publicly funded cancer research network in the nation. SWOG has more than 18,000 members in 45 states and nine foreign countries who design and conduct clinical trials to improve the lives of people with cancer. SWOG trials have led to the approval of 14 cancer drugs, changed more than 100 standards of cancer care, and saved more than 3 million years of human life. Learn more at swog.org, and follow us on Twitter at @SWOG.
About NRG Oncology
NRG Oncology conducts practice-changing, multi-institutional clinical and translational research to improve the lives of patients with cancer. Founded in 2012, NRG Oncology is a Pennsylvania-based nonprofit corporation that integrates the research of the legacy National Surgical Adjuvant Breast and Bowel Project (NSABP), Radiation Therapy Oncology Group (RTOG), and Gynecologic Oncology Group (GOG) programs. The research network seeks to carry out clinical trials with emphases on gender-specific malignancies, including gynecologic, breast, and prostate cancers, and on localized or locally advanced cancers of all types. NRG Oncology’s extensive research organization comprises multidisciplinary investigators, including medical oncologists, radiation oncologists, surgeons, physicists, pathologists, and statisticians, and encompasses more than 1,300 research sites located world-wide with predominance in the United States and Canada. NRG Oncology is supported primarily through grants from the National Cancer Institute (NCI) and is one of five research groups in the NCI’s National Clinical Trials Network.
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