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Multicenter Retrospective Analysis of Original versus Modified FOLFIRINOX in Metastatic Pancreatic Cancer: Results of the NAPOLEON Study.
Nakazawa, Junichi; Tsuruta, Nobuhiro; Shimokawa, Mototsugu; Kawahira, Machiko; Arima, Shiho; Ido, Akio; Koga, Futa; Ueda, Yujiro; Komori, Azusa; Otsu, Satoshi; Fukahori, Masaru; Makiyama, Akitaka; Taguchi, Hiroki; Honda, Takuya; Shibuki, Taro; Nio, Kenta; Ide, Yasushi; Ureshino, Norio; Mizuta, Toshihiko; Otsuka, Taiga; Shirakawa, Tsuyoshi; Mitsugi, Kenji.
Afiliação
  • Nakazawa J; Department of Medical Oncology, Kagoshima City Hospital, Kagoshima, Japan.
  • Tsuruta N; Department of Medical Oncology, Hamanomachi Hospital, Fukuoka, Japan.
  • Shimokawa M; Clinical Research Institute, National Kyushu Cancer Center, Fukuoka, Japan.
  • Kawahira M; Department of Biostatistics, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan.
  • Arima S; Department of Gastroenterology, Kagoshima Kouseiren Hospital, Kagoshima, Japan.
  • Ido A; Digestive and Lifestyle Diseases, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
  • Koga F; Digestive and Lifestyle Diseases, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
  • Ueda Y; Digestive and Lifestyle Diseases, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
  • Komori A; Department of Hepatobiliary and Pancreatology, Saga Medical Center Koseikan, 400 Kase-machi, Saga-shi, Saga, Japan.
  • Otsu S; Department of Hematology and Oncology, Japanese Red Cross Kumamoto Hospital, Kumamoto, Japan.
  • Fukahori M; Department of Medical Oncology and Hematology, Oita University Faculty of Medicine, Oita, Japan.
  • Makiyama A; Department of Medical Oncology and Hematology, Oita University Faculty of Medicine, Oita, Japan.
  • Taguchi H; Division of Gastroenterology, Department of Medicine, Kurume University School of Medicine, Fukuoka, Japan.
  • Honda T; Department of Hematology/Oncology, Japan Community Healthcare Organization Kyushu Hospital, Fukuoka, Japan.
  • Shibuki T; Cancer Center, Gifu University Hospital, Gifu, Japan.
  • Nio K; Department of Gastroenterology, Saiseikai Sendai Hospital, Kagoshima, Japan.
  • Ide Y; Department of Gastroenterology, Imamura General Hospital, Kagoshima, Japan.
  • Ureshino N; Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Mizuta T; Department of Internal Medicine, Imari Arita Kyoritsu Hospital, Saga, Japan.
  • Otsuka T; Department of Hepatobiliary and Pancreatic Oncology, National Cancer Center Hospital East, Chiba, Japan.
  • Shirakawa T; Department of Medical Oncology, Hamanomachi Hospital, Fukuoka, Japan.
  • Mitsugi K; Department of Medical Oncology, Sasebo Kyosai Hospital, Nagasaki, Japan.
Oncology ; 101(1): 22-31, 2023.
Article em En | MEDLINE | ID: mdl-36195058
ABSTRACT

INTRODUCTION:

Original FOLFIRINOX (oFFX) is more toxic than other regimens for patients with metastatic pancreatic cancer (mPC); therefore, a modified FFX (mFFX) regimen with a reduced dosage has been used in Japanese clinical practice. However, very few studies have compared these two regimens.

METHODS:

This study was conducted as part of a multicenter retrospective study of 318 patients with mPC across 14 centers in Japan (NAPOLEON study). To control for potential bias and confounders, we conducted a propensity score-adjusted analysis of patient characteristics and clinical outcomes.

RESULTS:

oFFX and mFFX were administered to 48 and 54 patients. More patients with younger age and poorer performance status were included in the oFFX group. The overall survival (OS; median, 11.6 vs. 11.3 months; hazard ratio [HR], 0.91; 95% confidence interval [CI], 0.60-1.40; p = 0.67), progression-free survival (PFS) (median, 6.3 vs. 5.7 months; HR, 0.85; 95% CI, 0.56-1.28; p = 0.44), and overall response rate (29 vs. 26%, p = 0.71) were not significantly different for the oFFX and mFFX groups. Thrombopenia and liver dysfunction were significantly more frequent with oFFX than with mFFX. The median received dose intensity of CPT-11 was higher with oFFX than with mFFX (299 vs. 270 mg/m2/week, p < 0.01). The propensity score-adjusted analysis revealed no statistically significant differences in OS and PFS between the two groups.

CONCLUSION:

In our data, there was no significant difference in efficacy between mFFX and oFFX, and mFFX has fewer adverse events.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas Tipo de estudo: Clinical_trials / Observational_studies Limite: Humans Idioma: En Revista: Oncology Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas Tipo de estudo: Clinical_trials / Observational_studies Limite: Humans Idioma: En Revista: Oncology Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão