A genotype-directed phase I-IV dose-finding study of irinotecan in combination with fluorouracil/leucovorin as first-line treatment in advanced colorectal cancer


Por: Marcuello, E, Paez, D, Pare, L, Salazar, J, Sebio, A, del Rio, E, Baiget, M

Publicada: 28 jun 2011
Resumen:
BACKGROUND: Infusional fluorouracil/leucovorin (FU/LV) plus irinotecan (FOLFIRI) is one of the standard first-line options for patients with metastatic colorectal cancer (mCRC). Irinotecan is converted into 7-ethyl-10-hydroxycamptothecin (SN-38) by a carboxylsterase and metabolised through uridine diphosphate glucuronosyl transferase (UGT1A1). The UGT1A1*28 allele has been associated with the risk of developing severe toxicities. The present trial was designed to define the maximum tolerated dose according to UGT1A1 genotype. This report focuses on the results of tolerance to different escalated doses of FOLFIRI first-line of chemotherapy. PATIENTS AND METHODS: Patients undergoing first-line treatment for mCRC and eligible for treatment with FOLFIRI were classified according to UGT1A1 genotype. A total of 94 patients were eligible for dose escalation of irinotecan. The starting dose of biweekly irinotecan was 180 mgm(-2) for the *1/*1, 110 mgm(-2) for the *1/*28 and 90 mgm(-2) for the *28/*28 genotypes. RESULTS: The dose of irinotecan was escalated to 450 mgm(-2) in patients with the *1/*1 genotype, to 390 mgm(-2) in those with the *1/*28 genotype and to 150 mgm(-2) in those with the *28/*28 genotype. Neutropenia and diarrhoea were the most common grade 3 or 4 toxicities. CONCLUSIONS: Our results demonstrated that the recommended dose of 180 mgm(-2) for irinotecan in FOLFIRI is considerably lower than the dose that can be tolerated for patients with the UGT1A1 *1/*1 and *1/*28 genotypes. The maximum tolerable dose (MTD) in patients with a high-risk UGT1A1 *28/*28 genotype is 30% lower than the standard dose of 180 mgm(-2). British Journal of Cancer (2011) 105, 53-57. doi:10.1038/bjc.2011.206 www.bjcancer.com Published online 7 June 2011 (C) 2011 Cancer Research UK

Filiaciones:
Marcuello, E:
 Univ Autonoma Barcelona, Dept Med Oncol, Barcelona 08025, Spain

Paez, D:
 Univ Autonoma Barcelona, Dept Med Oncol, Barcelona 08025, Spain

Pare, L:
 Univ Autonoma Barcelona, Dept Genet, Hosp Santa Creu & Sant Pau, Barcelona 08025, Spain

Salazar, J:
 Univ Autonoma Barcelona, Dept Genet, Hosp Santa Creu & Sant Pau, Barcelona 08025, Spain

 CIBERER, U 705, Barcelona, Spain

Sebio, A:
 Univ Autonoma Barcelona, Dept Med Oncol, Barcelona 08025, Spain

del Rio, E:
 Univ Autonoma Barcelona, Dept Genet, Hosp Santa Creu & Sant Pau, Barcelona 08025, Spain

Baiget, M:
 Univ Autonoma Barcelona, Dept Genet, Hosp Santa Creu & Sant Pau, Barcelona 08025, Spain
ISSN: 00070920





BRITISH JOURNAL OF CANCER
Editorial
NATURE PUBLISHING GROUP, MACMILLAN BUILDING, 4 CRINAN ST, LONDON N1 9XW, ENGLAND, GB
Tipo de documento: Article
Volumen: 105 Número: 1
Páginas: 53-57
WOS Id: 000292182400009
ID de PubMed: 21654688
imagen Green Published, Hybrid Gold

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