Attenuated FOLFIRINOX in the salvage treatment of gemcitabine-refractory advanced pancreatic cancer: a phase II study

Wiley - Tập 38 - Trang 1-8 - 2018
Jung Hoon Kim1, Sang-Cheol Lee2, Sung Yong Oh3, Seo-Young Song4, Namsu Lee5, Eun Mi Nam6, Soonil Lee7, In Gyu Hwang8, Hyo Rak Lee9, Kyu Taek Lee2, Sang-Byung Bae2, Han Jo Kim2, Joung Soon Jang8, Do Hyoung Lim7, Hyun Woo Lee10, Seok Yun Kang10, Jung Hun Kang1
1Department of Internal Medicine, Institute of Health Sciences, Gyeongsang National University, Jinju, Republic of Korea
2Divsion of Hematology and Oncology, Department of Internal Medicine, Soonchunhyang University Hospital Cheonan, Cheonan, Republic of Korea
3Department of Internal Medicine, Dong-A University Hospital, Busan, Republic of Korea
4Department of Internal Medicine, Kangwon National University School of Medicine, Chuncheon, Republic of Korea
5Divsion of Hematology and Oncology, Department of Internal Medicine, Soonchunhyang University Hospital Seoul, Seoul, Republic of Korea
6Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Republic of Korea
7Department of Internal Medicine, Dankook University Hospital, Cheonan, Republic of Korea
8Department of Internal Medicine, Chung-Ang University College of Medicine, Seoul, Republic of Korea
9Division of Hematology and Medical Oncology, Department of Internal Medicine, Korea Cancer Hospital, Seoul, Republic of Korea
10Department of Hematology-Oncology, Ajou University Hospital, Suwon, Republic of Korea

Tóm tắt

Combination therapy with oxaliplatin, irinotecan, fluorouracil, and leucovorin (FOLFIRINOX) chemotherapy drastically improves survival of advanced pancreatic cancer patients. However, the efficacy of FOLFIRINOX as a second-line treatment after gemcitabine failure has not been tested prospectively. We investigated the feasibility and safety of attenuated FOLFIRINOX in patients with gemcitabine-refractory advanced pancreatic cancer. A multicenter phase II prospective open-label, single-arm study was conducted at 14 hospitals. Patients with histologically proven invasive ductal pancreatic adenocarcinoma, a measurable or evaluable lesion, Eastern Cooperative Oncology Group performance status 0 or 1, adequate organ function, and aged 19 years or older were eligible. Attenuated FOLFIRINOX consisted of oxaliplatin 65 mg/m2, irinotecan 135 mg/m2, and leucovorin 400 mg/m2 injected intravenously on day 1 and 5-fluorouracil 2000 mg/m2 continuously infused intravenously over 46 h on days 1–2, repeated every 2 weeks. The primary endpoint was progression-free survival from the initiation of FOLFIRINOX. Secondary endpoints were the objective response rate, disease control rate, overall survival, safety, and tolerability. We estimated overall survival and progression-free survival using the Kaplan–Meier methods. We enrolled 39 patients from 14 institutions. The objective response rate was 10.3%, while the disease control rate was 64.1%. The 6-month and 1-year overall survival rates were 59.0% and 15.4%, respectively. Median progression-free survival and overall survival were 3.8 months (95% confidence interval [CI] 1.5–6.0 months) and 8.5 months (95% CI 5.6–11.4 months), respectively. Grade 3 or 4 adverse events were neutropenia (41.0%), nausea (10.3%), anorexia (10.3%), anemia (7.7%), mucositis (7.7%), pneumonia/pleural effusion (5.1%), and fatigue (5.1%). One treatment-related death attributable to septic shock occurred. Attenuated FOLFIRINOX may be promising as a second-line therapy for gemcitabine-refractory pancreatic cancer.

Tài liệu tham khảo

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