Literature DB >> 15456953

Weekly irinotecan (CPT-11) in 5-FU heavily pretreated and poor-performance-status patients with advanced colorectal cancer.

M Benavides1, P García-Alfonso, M Cobo, A Muñoz-Martín, S Gil-Calle, F Carabantes, E Villar, J Graupera, M Balcells, G Pérez-Manga.   

Abstract

Irinotecan (CPT-11) is an effective drug in patients with advanced colorectal cancer (CRC). Little is known about its efficacy and safety in previously treated patients with poor performance status. We prospectively evaluated the antitumor efficacy and safety of CPT-11 monotherapy in this setting. Thirty-four patients with poor performance status (Karnofsky score between 60 and 80) and/or progressing on one or more previous 5-FU-based chemotherapy lines for advanced colorectal adenocarcinoma were enrolled in this study. Treatment consisted of irinotecan (CPT-11) at 100 mg/m(2) administered as a 60-min iv infusion every week for four consecutive weeks followed by a 2-wk rest period until disease progression or unacceptable toxicity. The overall objective response rate (WHO criteria) for the 34 patients included was 20.6% [95% confidence interval (CI): 6.3%-34.9%]. Stable disease was obtained in 13 patients (38.2%) and 14 patients (41.2%) progressed. The median time to disease progression was 5.5 mo (range: 0.9-17.5) and the median survival was 8.3 mo (95% CI: 1.7-16.9). Overall, weekly CPT-11 was well tolerated with grade 3/4 neutropenia as the main hematological toxicity (11 patients: 32.4%; 14 infusions: 3.3%), and delayed diarrhea (10 patients: 29.4%; 16 infusions: 3.8%) as the main grade 3/4 non-hematological toxicity. In conclusion, weekly CPT-11 at 100 mg/m(2) for four consecutive weeks followed by a 2-wk rest period showed antitumor efficacy and may be safely administered to heavily pretreated patients with advanced colorectal cancer and a poor performance status. Weekly CPT-11 monotherapy may be considered as a therapeutic option for this population of patients.

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Year:  2004        PMID: 15456953     DOI: 10.1385/MO:21:3:255

Source DB:  PubMed          Journal:  Med Oncol        ISSN: 1357-0560            Impact factor:   3.064


  14 in total

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Journal:  J Clin Oncol       Date:  1997-08       Impact factor: 44.544

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Authors:  L B Saltz; J V Cox; C Blanke; L S Rosen; L Fehrenbacher; M J Moore; J A Maroun; S P Ackland; P K Locker; N Pirotta; G L Elfring; L L Miller
Journal:  N Engl J Med       Date:  2000-09-28       Impact factor: 91.245

4.  Efficacy of intravenous continuous infusion of fluorouracil compared with bolus administration in advanced colorectal cancer.

Authors:  P Piedbois; P Rougier; M Buyse; J Pignon; L Ryan; R Hansen; B Zee; B Weinerman; J Pater; C Leichman; J Macdonald; J Benedetti; J Lokich; J Fryer; G Brufman; R Isacson; A Laplanche; E Levy
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Journal:  J Clin Oncol       Date:  1997-01       Impact factor: 44.544

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Journal:  J Clin Oncol       Date:  1993-05       Impact factor: 44.544

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Journal:  Lancet       Date:  1998-10-31       Impact factor: 79.321

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Journal:  Lancet       Date:  1998-10-31       Impact factor: 79.321

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Authors:  E Lévy; P Piedbois; M Buyse; J P Pignon; P Rougier; L Ryan; R Hansen; B Zee; B Weinerman; J Pater; C Leichman; J Macdonald; J Benedetti; J Lokich; J Fryer; G Brufman; R Isacson; A Laplanche; E Quinaux; P Thirion
Journal:  J Clin Oncol       Date:  1998-11       Impact factor: 44.544

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  1 in total

1.  Treatment of patients with metastatic colorectal cancer and poor performance status: current evidence and challenges.

Authors:  Lucila Soares da Silva Rocha; Rachel P Riechelmann
Journal:  Clinics (Sao Paulo)       Date:  2018-09-21       Impact factor: 2.365

  1 in total

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