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Early results of a randomized two-by-two factorial phase II trial comparing neoadjuvant chemotherapy with two and four courses of cisplatin/S-1 and docetaxel/cisplatin/S-1 as neoadjuvant chemotherapy for locally advanced gastric cancer.
Aoyama, T; Nishikawa, K; Fujitani, K; Tanabe, K; Ito, S; Matsui, T; Miki, A; Nemoto, H; Sakamaki, K; Fukunaga, T; Kimura, Y; Hirabayashi, N; Yoshikawa, T.
Afiliación
  • Aoyama T; Department of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama.
  • Nishikawa K; Department of Surgery, Osaka National Hospital.
  • Fujitani K; Osaka General Medical Center, Department of Surgery, Osaka, Japan.
  • Tanabe K; Department of Gastrointestinal Surgery, Hiroshima University, Hiroshima.
  • Ito S; Department of Gastroenterological Surgery, Aichi Cancer Center, Nagoya.
  • Matsui T; Department of Surgery, Aichi Cancer Center Aichi Hospital, Okazaki.
  • Miki A; Department of Surgery, Kobe City Medical Center General Hospital, Kobe.
  • Nemoto H; Department of Surgery, Showa University Fujigaoka Hospital, Yokohama.
  • Sakamaki K; Department of Biostatistics and Epidemiology, Yokohama City University Medical Center, Yokohama.
  • Fukunaga T; Department of Surgery, Saint Marianna University, Kawasaki.
  • Kimura Y; Department of Surgery, Sakai City Hospital, Sakai.
  • Hirabayashi N; Department of Surgery, Hiroshima City Asa Citizens Hospital, Hiroshima, Japan.
  • Yoshikawa T; Department of Gastrointestinal Surgery, Kanagawa Cancer Center, Yokohama.
Ann Oncol ; 28(8): 1876-1881, 2017 Aug 01.
Article en En | MEDLINE | ID: mdl-28486692
ABSTRACT

BACKGROUND:

Neoadjuvant chemotherapy (NAC) is a promising method of improving the survival of resectable gastric cancer. Cisplatin/S-1 (CS) and docetaxel/cisplatin/S-1 (DCS) are both effective against metastatic gastric cancer. This report clarified the impact of these regimens on early endpoints, including the pathological responses, chemotherapy-related toxicities, and surgical results.

METHODS:

Patients with M0 and either T4 or T3 in case of junctional cancer or scirrhous type received two or four courses of cisplatin (60 mg/m2 at day 8)/S-1 (80 mg/m2 for 21 days with 1 week rest) or docetaxel (40 mg/m2 at day 1)/cisplatin (60 mg/m2 at day 1)/S-1 (80 mg/m2 for 14 days with 2 weeks rest) as NAC. Patients then underwent D2 gastrectomy and adjuvant S-1 chemotherapy for 1 year. The primary endpoint was the 3-year overall survival.

RESULTS:

Between October 2011 and September 2014, 132 patients were assigned to receive CS (n = 66; 33 in 2 courses and 33 in 4 courses) or DCS (n = 66; 33 in 2 courses and 33 in 4 courses). The respective major grade 3 or 4 hematological toxicities (CS/DCS) were leukocytopenia (14.1%/26.2%), neutropenia (29.7%/47.7%), anemia (14.1%/12.3%), and platelet reduction (3.1%/1.5%). The rate of pathological response, defined as a complete response or < 10% residual cancer remaining, was 19.4% in the CS group and 15.4% in the DCS group, and 15.6% in the two-course group and 19.0% in the 4-course group. The R0 resection rate was 72.7% in the CS group and 81.8% in the DCS group and 80.3% in the two-course group and the 74.2% in the four-course group. No treatment-related deaths were observed.

CONCLUSIONS:

Our results do not support three-drug therapy with a taxane over two-drug therapy, or any further treatment beyond two cycles as an attractive candidate for the test arm of NAC.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Gástricas / Protocolos de Quimioterapia Combinada Antineoplásica / Terapia Neoadyuvante Tipo de estudio: Clinical_trials Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Gástricas / Protocolos de Quimioterapia Combinada Antineoplásica / Terapia Neoadyuvante Tipo de estudio: Clinical_trials Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article