SWOG S1815: A Phase III Randomized Trial of Gemcitabine, Cisplatin, and Nab-Paclitaxel Versus Gemcitabine and Cisplatin in Newly Diagnosed, Advanced Biliary Tract Cancers
Abstract
PURPOSE SWOG S1815 was a randomized, open label phase III trial, evaluating gemcitabine, nab-paclitaxel, and cisplatin (GAP) versus gemcitabine and cisplatin (GC) in patients with newly diagnosed advanced biliary tract cancers (BTCs). METHODS Patients with newly diagnosed locally advanced unresectable or metastatic BTC, including intrahepatic cholangiocarcinoma (ICC) and extrahepatic cholangiocarcinoma (ECC) and gallbladder carcinoma (GBC), were randomly assigned 2:1 to either GAP (gemcitabine 800 mg/m 2 , cisplatin 25 mg/m 2 , and nab-paclitaxel 100 mg/m 2 intravenously once per day on days 1 and 8 of a 21-day cycle) or GC (gemcitabine 1,000 mg/m 2 and cisplatin 25 mg/m 2 intravenously once per day on days 1 and 8 of a 21-day cycle). RESULTS Among 452 randomly assigned participants, 441 were eligible and analyzable, 67% with ICC, 16% with GBC, and 17% with ECC. There was no significant difference in overall survival (OS) between GAP versus GC. Median OS with GAP was 14.0 months (95% CI, 12.4 to 16.1) and 13.6 months with GC (95% CI, 9.7 to 16.6); hazard ratio (HR), 0.91 (95% CI, 0.72 to 1.14); P = .41. Median progression-free survival (PFS) was similar between groups with median PFS for GAP being 7.5 months (95% CI, 6.4 to 8.5) versus 6.3 months for GC (95% CI, 4.4 to 8.2); HR, 0.89 (95% CI, 0.71 to 1.12); P = .32. In exploratory subset analyses, the OS and PFS benefits of GAP versus GC treatment were greater in locally advanced disease compared with metastatic disease, although not statistically significant (interaction P = .14 for OS and P = .17 for PFS). Moreover, GAP versus GC showed greater improvement in PFS among participants with GBC than those with ICC or ECC (interaction P = .01), but not OS (interaction P = .28). CONCLUSION The addition of a taxane in the GAP regimen to the standard gemcitabine-cisplatin regimen did not improve OS in newly diagnosed BTC. More toxicity was encountered with GAP versus GC.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (22)
Rachna T. Shroff
Gentry King
Fred Hutchinson Cancer Center, University of Washington, Seattle, WA
Sarah Colby
Fred Hutch Cancer Center and SWOG Statistics and Data Management Center, Seattle, WA
Aaron J. Scott
University of Arizona Cancer Center, Tucson, AZ
Mitesh J. Borad
Department of Oncology, Mayo Clinic, Phoenix, AZ
Laura Goff
Vanderbilt-Ingram Cancer Center, Nashville, TN
Khalid Matin
Division of Hematology and Oncology, Virginia Commonwealth University, Richmond
Amit Mahipal
Department of Oncology, University Hospitals Seidman Cancer Center, Case Western Reserve University, Cleveland, OH
Aparna Kalyan
Hematology and Oncology, Developmental Therapeutics Institute, Northwestern University, Chicago, IL
Milind M. Javle
Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX
Imane El Dika
Memorial Sloan Kettering Cancer Center, New York, NY
Benjamin Tan
Washington University Siteman Cancer Center, St Louis, MO
Puneet Cheema
Metro Minnesota Community Oncology Research Consortium/Saint John's Hospital, St Louis Park, MN
Anuj Patel
Dana-Farber Harvard Cancer Center, Boston, MA
Renuka Iyer
2roswell park cancer center, buffalo, United States
R. Katie Kelley
Hellen Diller Family Comprehensive Cancer Center, University of California San Francisco Medical Center, San Francisco, CA
Jaykumar Thumar
Yale Cancer Center, New Haven, CT
Anthony El-Khoueiry
Department of Clinical Medicine, Keck School of Medicine, University of Southern California Norris Comprehensive Cancer Center, Los Angeles, CA
Katherine A. Guthrie
Fred Hutchinson Cancer Center; and SWOG Statistics and Data Management Center, Seattle, WA
E. Gabriela Chiorean
Division of Hematology-Oncology, Department of Medicine, University of Washington School of Medicine, Seattle, WA
Howard Hochster
Rutgers University, Newark, NJ
Philip A. Philip
Department of Oncology and Pharmacology, Wayne State University School of Medicine, Detroit, MI