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K. J. Scanlon, E. M. Newman, Y. Lu and D. G. Priest, “Biochemical Basis for Cisplatin and 5-Fluorouracil Synergism in Human Ovarian Carcinoma Cells,” Proceedings of the National Academy of Sciences of the United States of America, Vol. 83, No. 23, 1986, pp. 8923-8925. doi:10.1073/pnas.83.23.8923

has been cited by the following article:

• TITLE: Dose-Dense Regimen of Cisplatin and Infusional Fluorouracil in Advanced Gastric Cancer—A Single Institution Experience

  AUTHORS: Ofer Purim, Yulia Kundel, Roni Shapira, Baruch Brenner

  KEYWORDS: Gastric Cancer; Dose-Dense; Cisplatin; Fluorouracil

  JOURNAL NAME: Journal of Cancer Therapy, Vol.4 No.2, April 15, 2013

  ABSTRACT: Chemotherapy with continuous infusion of 5-fluorouracil and cisplatin in a monthly schedule is one of the most common regimens in the treatment of advanced gastric cancer. In this study, we evaluated the efficacy and safety of a dosedense administration of this regimen in this patient population. Sixty-six consecutive patients with previously untreated histologically confirmed unresectable or metastatic gastric adenocarcinoma were treated with a 2-hour infusion of cisplatin 100 mg/m2 followed by continuous infusion of 5-fluorouracil 1000 mg/m2/day for 5 days, every 21 days. The most common grade ≥3 toxicities were fatigue (42%), nausea/vomiting (30%) and leucopenia (12%). Four patients (6%) died from treatment-related toxicity. The response rate was 35%, the median progression-free survival was 4.3 months and the median survival was 5.9 months. In light of these results, the dose-dense approach seems to offer little, if any, benefit compared with the standard regimens.