Literature DB >> 12544262

Safety and efficacy of outpatient treatment with CPT-11 plus bolus folinic acid/5-fluorouracil as first-line chemotherapy for metastatic colorectal cancer.

Markus Moehler1, Tanja Hoffmann, Christine Zanke, Horst Hohl, Helmut Burg, Peter Ehscheid, Peter Schwindt, Bernd Adami, Martin Schroeder, Ortwin Klein, Michael Baldus, Peter R Galle, Michael Heike.   

Abstract

The combination of irinotecan (CPT-11), bolus 5-fluorouracil (5-FU) and folinic acid (FA) (Saltz regimen) has recently been questioned as first-line chemotherapy for metastatic colorectal cancer after high early death rates due to gastrointestinal and thromboembolic events were reported in two US trials. Therefore, we carefully evaluated the safety and efficacy of this regimen, with high value placed on the management of delayed diarrhea. Forty-six patients with metastatic colorectal cancer received this first-line treatment in nine German outpatient clinics. Dose reductions were mandatory from the first cycle in case of toxicity grade >2. Chemotherapy was administered only to diarrhea-free patients. During a total of 175 cycles administered treatments were delayed for 1 week in 11.6% and given at a reduced dose in 14.5%. All and 40 patients were evaluable for toxicity and response, respectively. Grade 3/4 toxicities included diarrhea (n=10), leukopenia (n=9), neutropenia (n=3) and anemia (n=4). One non-fatal pulmonary embolism occurred. Four complete responses (CR) and 10 partial responses were seen, for an overall response rate of 35%. In addition, 16 patients (40%) had stable disease. Resectability of liver metastases was achieved in three patients, including one pathologically confirmed CR. Median progression-free and overall survival were 5 and 13 months, respectively. We conclude that outpatient treatment with the Saltz regimen was well tolerated. Severe gastrointestinal toxicity and thromboembolic events were rarely observed and never fatal. As down-staging was possible, combinations of CPT-11 and FA/5-FU should be further investigated in neoadjuvant protocols. Copyright 2003 Lippincott Williams & Wilkins

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12544262     DOI: 10.1097/00001813-200301000-00011

Source DB:  PubMed          Journal:  Anticancer Drugs        ISSN: 0959-4973            Impact factor:   2.248


  4 in total

1.  Weekly irinotecan plus UFT and leucovorin as first-line chemotherapy of patients with advanced colorectal cancer.

Authors:  M Méndez; P G Alfonso; E Pujol; E González; C Castañon; P Cerezuela; Y López-Mateos; J J Cruz
Journal:  Invest New Drugs       Date:  2005-06       Impact factor: 3.850

2.  Capecitabine and irinotecan with and without bevacizumab for advanced colorectal cancer patients.

Authors:  Markus Moehler; Martin-F Sprinzl; Murad Abdelfattah; Carl-C Schimanski; Bernd Adami; Werner Godderz; Klaus Majer; Dimitri Flieger; Andreas Teufel; Juergen Siebler; Thomas Hoehler; Peter-R Galle; Stephan Kanzler
Journal:  World J Gastroenterol       Date:  2009-01-28       Impact factor: 5.742

3.  A phase II experience with neoadjuvant irinotecan (CPT-11), 5-fluorouracil (5-FU) and leucovorin (LV) for colorectal liver metastases.

Authors:  Oliver F Bathe; Scott Ernst; Francis R Sutherland; Elijah Dixon; Charles Butts; David Bigam; David Holland; Geoffrey A Porter; Jennifer Koppel; Scot Dowden
Journal:  BMC Cancer       Date:  2009-05-20       Impact factor: 4.430

4.  Irinotecan plus folinic acid/continuous 5-fluorouracil as simplified bimonthly FOLFIRI regimen for first-line therapy of metastatic colorectal cancer.

Authors:  Andreas Teufel; Silke Steinmann; Jürgen Siebler; Christiane Zanke; Herbert Hohl; Bernd Adami; M Schroeder; O Klein; Thomas Höhler; Peter R Galle; Michael Heike; Markus Moehler
Journal:  BMC Cancer       Date:  2004-07-20       Impact factor: 4.430

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.