Literature DB >> 9669654

5-Fluorouracil, high-dose folinic acid and mitomycin C combination chemotherapy in previously treated patients with advanced colorectal carcinoma.

J F Seitz1, H Perrier, M Giovannini, G Capodano, D Bernardini, V J Bardou.   

Abstract

The aim of this study was to evaluate the efficacy and tolerance of second-line continuous 5-fluorouracil (5FU) chemotherapy combined with folinic acid and mitomycin C in patients with advanced colorectal cancer who progressed on first-line chemotherapy. From June 1992 to April 1994, 24 consecutive patients, median age 59.7 years (range 41-73), performance status (PS) 0 to 2, were treated as second-line chemotherapy with mitomycin C, 7 mg/m2 every 4 weeks, folinic acid 200 mg/m2/day as a 2 h infusion followed by 400 mg/m2 of 5FU bolus and 600 mg/m2 continuous 5FU infusion for 22 h on days 1 and 2 and every 14 days; 19 patients did not respond to folinic acid and 5FU bolus regimen (in 2 patients, this was associated with pirarubicin in a continuous hepatic artery infusion) and 3 did not respond to irinotecan; 2 patients had disease progression during adjuvant chemotherapy with folinic acid and 5FU bolus. Tumor response was assessed every 12 weeks. One patient died before evaluation and 1 was lost to follow-up after 3 cycles; 7/24 patients had an objective response (29.2%, 95% confidence interval (CI): 11.0-47.4) including 2 complete responses; 7 additional patients had stable disease or minor response. Mean duration of response was 7.5 months. Median survival was 10 months and survival at 1 year was 39.4% (95% CI: 4-59.4). One patient who had a disease progression under irinotecan presented an objective response. No iatrogenic deaths occurred, nor was any grade 3 or 4 myelotoxicity seen. No hand-foot syndrome nor any cardiotoxicity arose but 2 grade II alopecia were seen. Digestive toxicities were the most frequent but with only 4 grade III toxicities (1 vomiting, 1 mucositis and 2 diarrhea) and no grade IV. With nearly 30% objective response and acceptable toxicity this treatment seems to offer a good alternative in the treatment of advanced colorectal cancers after the failure of first-line chemotherapy.

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Year:  1998        PMID: 9669654     DOI: 10.1179/joc.1998.10.3.258

Source DB:  PubMed          Journal:  J Chemother        ISSN: 1120-009X            Impact factor:   1.714


  5 in total

1.  Activity of boanmycin against colorectal cancer.

Authors:  Y C Deng; Y S Zhen; S Zheng; Y C Xue
Journal:  World J Gastroenterol       Date:  2001-02       Impact factor: 5.742

2.  A phase II study of mitomycin-C and S-1 as third-line chemotherapy in patients with advanced colorectal cancer.

Authors:  Jung Han Kim; Hyeong Su Kim; Dae Ro Choi; Geundoo Jang; Jung Hye Kwon; Ho Young Kim; Joo Young Jung; Hyo Jung Kim; Hun Ho Song; Yun Ho Shin; So Young Jung; Byung Chun Kim; Dae Young Zang
Journal:  Oncol Lett       Date:  2011-07-27       Impact factor: 2.967

3.  Sirolimus, bevacizumab, 5-Fluorouracil and irinotecan for advanced colorectal cancer: a pilot study.

Authors:  Francois Ghiringhelli; Boris Guiu; Bruno Chauffert; Sylvain Ladoire
Journal:  World J Gastroenterol       Date:  2009-09-14       Impact factor: 5.742

Review 4.  Complications of hepatic artery infusion: a review of 4580 reported cases.

Authors:  K T Barnett; M P Malafa
Journal:  Int J Gastrointest Cancer       Date:  2001

5.  Protracted infusional 5-fluorouracil plus high-dose folinic acid combined with bolus mitomycin C in patients with gastrointestinal cancer: a phase I/II dose escalation study.

Authors:  J T Hartmann; K Oechsle; D Quietzsch; A Wein; R D Hofheinz; F Honecker; O Nehls; C-H Köhne; G Käfer; L Kanz; C Bokemeyer
Journal:  Br J Cancer       Date:  2003-12-01       Impact factor: 7.640

  5 in total

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