Assessing clinical benefit response in the treatment of gastric malignant ascites with non-measurable lesions: a multicenter phase II trial of paclitaxel for malignant ascites secondary to advanced/recurrent gastric cancer

Assessing clinical benefit response in the treatment of gastric malignant ascites with non-measurable lesions: a multicenter phase II trial of paclitaxel for malignant ascites secondary to advanced/recurrent gastric cancer

  • نوع فایل : کتاب
  • زبان : انگلیسی
  • مؤلف : Haruhiko Imamoto Koji Oba Junichi Sakamoto Hiroyasu Iishi Hiroyuki Narahara Takeyoshi Yumiba Takashi Morimoto Masaki Nakamura Noboru Ori
  • چاپ و سال / کشور: 2011

Description

Background Paclitaxel has shown promise against advanced gastric cancer and associated malignant ascites with non-measurable lesions. In order to evaluate the therapeutic effect of paclitaxel against malignant gastric ascites, a prospective phase II clinical trial was designed according to our previously proposed criteria represented by the clinical benefit response in gastric cancer (CBR-GC) criteria and the five-point method (5PM). Methods Patients with advanced gastric cancer with malignant ascites were treated with 1-h intravenous (i.v.) infusions of 80 mg/m2 of paclitaxel weekly over a 3-week cycle on days 1, 8, and 15, followed by 1 week of rest. Therapeutic responses were measured according to the CBR-GC criteria and the 5PM. Results The CBR-GC criteria showed improved ascites volume and functional status in 39.1% of patients. A positive CBR-GC response in abdominal girth was seen in 31.3% of patients, and this was significantly correlated with the 5PM-estimated change in ascites volume (p\0.001). The median number of treatment cycles was 3 (range 1–12). The most common non-hematological toxicity was anorexia, in 22.2% of patients. Conclusion Weekly i.v. paclitaxel is a safe and effective chemotherapeutic regimen based on validated CBR-CG criteria.
Gastric Cancer (2011) 14:81–90 DOI 10.1007/s10120-011-0016-6 Received: 30 September 2010 / Accepted: 21 November 2010 / Published online: 17 February 2011
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