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Conversion Surgery for Unresectable Pancreatic Cancer Treated With FOLFIRINOX or Gemcitabine Plus Nab-paclitaxel.
Ide, Yasushi; Otsuka, Taiga; Shimokawa, Mototsugu; Koga, Futa; Ueda, Yujiro; Nakazawa, Junichi; Komori, Azusa; Otsu, Satoshi; Arima, Shiho; Fukahori, Masaru; Makiyama, Akitaka; Shinohara, Yudai; Ueno, Shohei; Taguchi, Hiroki; Honda, Takuya; Shibuki, Taro; Nio, Kenta; Ureshino, Norio; Mizuta, Toshihiko; Mitsugi, Kenji; Shirakawa, Tsuyoshi.
Afiliación
  • Ide Y; Department of Internal Medicine, Karatsu Red Cross Hospital, Saga, Japan.
  • Otsuka T; Department of Internal Medicine, National Hospital Organization Saga Hospital, Saga, Japan.
  • Shimokawa M; Department of Medical Oncology, Saga Medical Center Koseikan, Saga, Japan; otsuka-t@umin.ac.jp.
  • Koga F; Department of Internal Medicine, Minato Medical Clinic, Fukuoka, Japan.
  • Ueda Y; Clinical Research Institute, National Kyushu Cancer Center, Fukuoka, Japan.
  • Nakazawa J; Department of Biostatistics, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan.
  • Komori A; Department of Hepatobiliary and Pancreatology, Saga Medical Center Koseikan, Saga, Japan.
  • Otsu S; Department of Hematology and Oncology, Japanese Red Cross Kumamoto Hospital, Kumamoto, Japan.
  • Arima S; Department of Medical Oncology, Kagoshima City Hospital, Kagoshima, 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.
  • Shinohara Y; Digestive and Lifestyle Diseases, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
  • Ueno S; Department of Internal Medicine, Division of Gastroenterology, Kurume University Hospital, Fukuoka, Japan.
  • Taguchi H; Department of Hematology/Oncology, Japan Community Healthcare Organization Kyushu Hospital, Fukuoka, Japan.
  • Honda T; Cancer Center, Gifu University Hospital, Gifu, Japan.
  • Shibuki T; Department of Hematology/Oncology, Japan Community Healthcare Organization Kyushu Hospital, Fukuoka, Japan.
  • Nio K; Department of Hematology/Oncology, Japan Community Healthcare Organization Kyushu Hospital, Fukuoka, Japan.
  • Ureshino N; Department of Gastroenterology, Saiseikai Sendai Hospital, Kagoshima, Japan.
  • Mizuta T; Department of Gastroenterology, Imamura General Hospital, Kagoshima, Japan.
  • Mitsugi K; Department of Gastroenterology and Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
  • Shirakawa T; Department of Internal Medicine, Imari Arita Kyoritsu Hospital, Saga, Japan.
Anticancer Res ; 43(4): 1817-1826, 2023 Apr.
Article en En | MEDLINE | ID: mdl-36974805
ABSTRACT
BACKGROUND/

AIM:

Recent advances in chemotherapy have made significant progress in conversion surgery (CS) for unresectable pancreatic cancer (uPC). However, the success rate and efficacy of CS have not been fully demonstrated in patients with uPC treated with FOLFIRINOX (FFX) or gemcitabine plus nab-paclitaxel (GnP). PATIENTS AND

METHODS:

We retrospectively reviewed the records of 318 patients with uPC who received FFX or GnP as first-line chemotherapy. The efficacy in the CS group, defined as undergoing complete resection after chemotherapy, was analyzed, and compared with the non-CS group; then, contributing factors to achieving CS were extracted. We also analyzed differences in the efficacy of CS between locally advanced pancreatic cancer (LAPC) and metastatic pancreatic cancer (MPC).

RESULTS:

Overall, CS was achieved in 4.3% of cases, eight patients (13.3%) with LAPC and five (2.1%) with MPC. Contributing factors to CS were LAPC, no liver metastasis, CA19-9 ≤37, and chemotherapy response. After adjusting for these, overall survival was significantly better in the CS group than in the non-CS group [median of 32.9 vs. 11.3 months; adjusted hazard ratio (HR)=0.32; 95% confidence interval (CI)=0.14-0.70; p<0.01]. Median relapse-free survival duration after CS was 19.1 and 18.1 months in the LAPC-CS and MPC-CS group, respectively (p=0.84). The median post-conversion survival was 27.6 months in the entire CS group, 43.8 months in the LAPC-CS group and 21.3 months in the MPC-CS group.

CONCLUSION:

CS was achieved in 13.3% of LAPC and 2.1% of MPC cases. If possible, CS can markedly improve prognosis, even in MPC.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Anticancer Res Año: 2023 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Anticancer Res Año: 2023 Tipo del documento: Article País de afiliación: Japón