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Efficacy and Safety of Bolus 5-Fluorouracil and L-Leucovorin as Salvage Chemotherapy for Oral Fluoropyrimidine-Resistant Unresectable or Recurrent Gastric Cancer: A Single Center Experience.
Muranaka, Tetsuhito; Yuki, Satoshi; Komatsu, Yoshito; Sawada, Kentaro; Harada, Kazuaki; Kawamoto, Yasuyuki; Nakatsumi, Hiroshi; Sakamoto, Naoya.
Afiliação
  • Muranaka T; Cancer Center, Hokkaido University Hospital, Sapporo, Japan.; Department of Gastroenterology and Hepatology, Hokkaido University Hospital, Sapporo, Japan.
  • Yuki S; Department of Gastroenterology and Hepatology, Hokkaido University Hospital, Sapporo, Japan.
  • Komatsu Y; Cancer Center, Hokkaido University Hospital, Sapporo, Japan.
  • Sawada K; Department of Gastroenterology and Hepatology, Hokkaido University Hospital, Sapporo, Japan.
  • Harada K; Cancer Center, Hokkaido University Hospital, Sapporo, Japan.
  • Kawamoto Y; Cancer Center, Hokkaido University Hospital, Sapporo, Japan.
  • Nakatsumi H; Cancer Center, Hokkaido University Hospital, Sapporo, Japan.
  • Sakamoto N; Department of Gastroenterology and Hepatology, Hokkaido University Hospital, Sapporo, Japan.
J Gastric Cancer ; 16(3): 177-181, 2016 Sep.
Article em En | MEDLINE | ID: mdl-27752395
ABSTRACT

PURPOSE:

The International Organization for Standardization-5fluorouracil (FU) 10 trial found that bolus 5-FU and l-leucovorin was not inferior to S-1 in the treatment of gastric cancer (GC). Continuous 5-FU and the rapid injection of 5-FU have different anti-cancer effects. Thus, bolus 5-FU and l-leucovorin treatment might be useful for oral FU-resistant GC. MATERIALS AND

METHODS:

We retrospectively analyzed the medical records of all patients with S-1 or capecitabine-resistant, unresectable, or recurrent GC treated with bolus 5-FU and l-leucovorin between January 2010 and December 2015 at Hokkaido University Hospital. The bolus 5-FU and l-leucovorin regimen consisted of intravenous l-leucovorin (250 mg/m2/2 h) and bolus 5-FU (600 mg/m2) administered once weekly followed by a 2-week rest period; each cycle was repeated every 8 weeks.

RESULTS:

A total of 14 patients were identified. The disease control rate was 35.7%. The median progression-free survival was 1.6 months (95% confidence interval [CI], 1.3~2.0 months), and the median overall survival was 6.3 months (95% CI, 4.7~7.9 months). No patient died from treatment-related causes. The most common severe adverse event associated with bolus 5-FU and l-leucovorin was neutropenia, which occurred in 21.4% of patients.

CONCLUSIONS:

Bolus 5-FU and l-leucovorin treatment might be useful for oral FU-resistant GC. We are planning a multi-center prospective phase II trial to evaluate the efficacy and safety of bolus 5-FU and l-leucovorin treatment for pre-treated unresectable or recurrent GC to confirm the results of this limited, retrospective study.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Idioma: En Ano de publicação: 2016 Tipo de documento: Article