A systematic review of FOLFOXIRI chemotherapy for the first-line treatment of metastatic colorectal cancer: improved efficacy at the cost of increased toxicity
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作者:
Montagnani, F.
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S Giuseppe Hosp, Dept Oncol, Oncol Unit, Florence, ItalyS Giuseppe Hosp, Dept Oncol, Oncol Unit, Florence, Italy
Montagnani, F.
[1
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Chiriatti, A.
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Univ Siena, Sch Med, Nurse Med Sch, I-53100 Siena, ItalyS Giuseppe Hosp, Dept Oncol, Oncol Unit, Florence, Italy
Chiriatti, A.
[2
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Turrisi, G.
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机构:S Giuseppe Hosp, Dept Oncol, Oncol Unit, Florence, Italy
Turrisi, G.
Francini, G.
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Univ Siena, Sch Med, Med Oncol Unit, Giorgio Segre Dept Pharmacol, I-53100 Siena, ItalyS Giuseppe Hosp, Dept Oncol, Oncol Unit, Florence, Italy
Francini, G.
[3
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Fiorentini, G.
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机构:S Giuseppe Hosp, Dept Oncol, Oncol Unit, Florence, Italy
Fiorentini, G.
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[1] S Giuseppe Hosp, Dept Oncol, Oncol Unit, Florence, Italy
Aim The simultaneous administration of irinotecan, 5-fluorouracil, folinic acid and oxaliplatin (FOLFOXIRI) has been compared with standard 5-fluorouracil, folinic acid and irinotecan (FOLFIRI) in randomized trials in metastatic colorectal cancer patients. A superior efficacy of FOLFOXIRI has been reported by some authors, but others have failed to show any differences and do not recommend its use because of greater cost and toxicity. We performed a systematic review of the literature to analyse efficacy and toxicity of FOLFOXIRI. Method Odds ratios (OR) with 95% confidence intervals (CI) were used to analyse dichotomous variables. Hazard ratios (HR) for progression and death were combined with an inverse variance method based on logarithmic conversion. A fixed-effect model and Mantel-Haenszel's method were used. Heterogeneity was tested with Cochrane's Q test and I-2 test. Results A significant increase in response rate (OR 2.04; P < 0.01) was associated with treatment by FOLFOXIRI and a benefit was also shown by the HR for progression (HR 0.72; P < 0.01) and death (HR 0.71; P < 0.01). Analysis for toxicity found a significant increase associated with FOLFOXIRI except for anaemia, fatigue and febrile neutropenia. Conclusion FOLFOXIRI confers significant benefit in progression-free survival, survival, response and R0 resection rates but is more toxic compared with FOLFIRI.
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Univ Lisbon, Res Inst Med iMed ULisboa, Fac Pharm, Ave Prof Gama Pinto, P-1649003 Lisbon, Portugal
Hosp Santa Maria, Ctr Hosp Lisboa Norte, Lisbon, PortugalUniv Lisbon, Res Inst Med iMed ULisboa, Fac Pharm, Ave Prof Gama Pinto, P-1649003 Lisbon, Portugal
Marques, Rui Pedro
Duarte, Goncalo S.
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Univ Lisbon, Fac Med, Lab Farmacol Clin & Terapeut, Lisbon, Portugal
Inst Med Mol, Clin Pharmacol Unit, Lisbon, Portugal
Univ Lisbon, Fac Med, Ctr Estudos Med Baseada Evidencia, Lisbon, PortugalUniv Lisbon, Res Inst Med iMed ULisboa, Fac Pharm, Ave Prof Gama Pinto, P-1649003 Lisbon, Portugal
Duarte, Goncalo S.
Sterrantino, Carmelo
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Univ York, Ctr Reviews & Disseminat, York, N Yorkshire, England
Univ Messina, Policlin G Martino, Dept Clin & Expt Med, Messina, ItalyUniv Lisbon, Res Inst Med iMed ULisboa, Fac Pharm, Ave Prof Gama Pinto, P-1649003 Lisbon, Portugal
Sterrantino, Carmelo
Pais, Helena Luna
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Hosp Santa Maria, Ctr Hosp Lisboa Norte, Lisbon, PortugalUniv Lisbon, Res Inst Med iMed ULisboa, Fac Pharm, Ave Prof Gama Pinto, P-1649003 Lisbon, Portugal
Pais, Helena Luna
Quintela, Antonio
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Hosp Santa Maria, Ctr Hosp Lisboa Norte, Lisbon, PortugalUniv Lisbon, Res Inst Med iMed ULisboa, Fac Pharm, Ave Prof Gama Pinto, P-1649003 Lisbon, Portugal
Quintela, Antonio
Martins, Ana Paula
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Univ Lisbon, Res Inst Med iMed ULisboa, Fac Pharm, Ave Prof Gama Pinto, P-1649003 Lisbon, PortugalUniv Lisbon, Res Inst Med iMed ULisboa, Fac Pharm, Ave Prof Gama Pinto, P-1649003 Lisbon, Portugal
Martins, Ana Paula
Costa, Joao
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Univ Lisbon, Fac Med, Lab Farmacol Clin & Terapeut, Lisbon, Portugal
Inst Med Mol, Clin Pharmacol Unit, Lisbon, Portugal
Univ Lisbon, Fac Med, Ctr Estudos Med Baseada Evidencia, Lisbon, PortugalUniv Lisbon, Res Inst Med iMed ULisboa, Fac Pharm, Ave Prof Gama Pinto, P-1649003 Lisbon, Portugal