Low‐dose gemcitabine plus nab‐paclitaxel versus standard‐dose gemcitabine plus nab‐paclitaxel in elderly patients with metastatic pancreatic cancer: A randomized Phase II trial
Ken Kamata,
Hajime Imai,
Hisakazu Matsumoto,
Yukitaka Yamashita,
Takao Kato,
Katsuhisa Nishi,
Shunsuke Omoto,
Kosuke Minaga,
Kentaro Yamao,
Tomoko Hyodo,
Sung‐Woon Im,
Akane Hara,
Tomoe Yoshikawa,
Rei Ishikawa,
Ayana Okamoto,
Tomohiro Yamazaki,
Atsushi Nakai,
Kazuomi Ueshima,
Yasutaka Chiba,
Mamoru Takenaka,
Tomohiro Watanabe,
Masayuki Kitano,
Masatoshi Kudo
Affiliations
Ken Kamata
Department of Gastroenterology and Hepatology Kindai University Faculty of Medicine Osaka Japan
Hajime Imai
Department of Gastroenterology Okanami General Hospital Mie Japan
Hisakazu Matsumoto
Department of Gastroenterology Japanese Red Cross Wakayama Medical Center Wakayama Japan
Yukitaka Yamashita
Department of Gastroenterology Japanese Red Cross Wakayama Medical Center Wakayama Japan
Takao Kato
Department of Gastroenterology Hyogo Prefectural Awaji Medical Center Hyogo Japan
Katsuhisa Nishi
Department of Gastroenterology Hyogo Prefectural Awaji Medical Center Hyogo Japan
Shunsuke Omoto
Department of Gastroenterology and Hepatology Kindai University Faculty of Medicine Osaka Japan
Kosuke Minaga
Department of Gastroenterology and Hepatology Kindai University Faculty of Medicine Osaka Japan
Kentaro Yamao
Department of Gastroenterology and Hepatology Kindai University Faculty of Medicine Osaka Japan
Tomoko Hyodo
Department of Radiology Kindai University Faculty of Medicine Osaka‐Sayama Japan
Sung‐Woon Im
Department of Radiology Kindai University Faculty of Medicine Osaka‐Sayama Japan
Akane Hara
Department of Gastroenterology and Hepatology Kindai University Faculty of Medicine Osaka Japan
Tomoe Yoshikawa
Department of Gastroenterology and Hepatology Kindai University Faculty of Medicine Osaka Japan
Rei Ishikawa
Department of Gastroenterology and Hepatology Kindai University Faculty of Medicine Osaka Japan
Ayana Okamoto
Department of Gastroenterology and Hepatology Kindai University Faculty of Medicine Osaka Japan
Tomohiro Yamazaki
Department of Gastroenterology and Hepatology Kindai University Faculty of Medicine Osaka Japan
Atsushi Nakai
Department of Gastroenterology and Hepatology Kindai University Faculty of Medicine Osaka Japan
Kazuomi Ueshima
Department of Gastroenterology and Hepatology Kindai University Faculty of Medicine Osaka Japan
Yasutaka Chiba
Clinical Research Center Kindai University Hospital Osaka Japan
Mamoru Takenaka
Department of Gastroenterology and Hepatology Kindai University Faculty of Medicine Osaka Japan
Tomohiro Watanabe
Department of Gastroenterology and Hepatology Kindai University Faculty of Medicine Osaka Japan
Masayuki Kitano
Second Department of Internal Medicine Wakayama Medical University School of Medicine Wakayama Japan
Masatoshi Kudo
Department of Gastroenterology and Hepatology Kindai University Faculty of Medicine Osaka Japan
Abstract Background and Aim A multicenter, open‐label randomized Phase II trial was conducted to determine whether low‐dose gemcitabine plus nab‐paclitaxel (GnP) could improve tolerability and show equivalent efficacy to the standard‐dose GnP for elderly patients with metastatic pancreatic cancer. Methods Consecutive patients aged ≥65 years with metastatic pancreatic cancer who presented at one of four Japanese referral centers between November 2016 and January 2021 were enrolled. The 60 patients were randomly assigned to low‐ or standard‐dose groups with a 1:1 ratio. Patients in the low‐dose GnP group received gemcitabine at a dose of 250 mg/m2 and nab‐paclitaxel at 125 mg/m2. Results Low‐dose GnP significantly decreased the rate of cases requiring dose reduction (16.7% vs 63.3%). The response rate (36.7% vs 33.3%) and progression‐free survival (7.3 vs 8 months) were comparable between the low‐ and standard‐dose groups as determined by independent review. The difference in the median overall survival between the two groups was not significant (7.9 vs 12 months). The proportion of patients with hematologic and non‐hematologic treatment‐related adverse events was comparable between the two groups. Conclusion Low‐dose GnP had an equivalent efficacy to conventional therapy; however, it did not reduce adverse events.