A systematic review of raltitrexed-based first-line chemotherapy in advanced colorectal cancer

被引:38
作者
Barni, Sandro [1 ]
Ghidini, Antonio [2 ]
Coinu, Andrea [1 ]
Borgonovo, Karen [1 ]
Petrelli, Fausto [1 ]
机构
[1] Treviglio Hosp, Dept Oncol, Med Oncol Unit, I-24047 Treviglio, BG, Italy
[2] Casa Cura Igea, Med Oncol, Milan, Italy
关键词
colorectal cancer; combination chemotherapy; first line; metastatic; overall survival; raltitrexed; toxicity; PHASE-II TRIAL; RANDOMIZED-TRIAL; PLUS OXALIPLATIN; IRINOTECAN; 5-FLUOROURACIL; CARDIOTOXICITY; FLUOROPYRIMIDINES; CAPECITABINE; FLUOROURACIL; LEUCOVORIN;
D O I
10.1097/CAD.0000000000000133
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Raltitrexed is a thymidylate synthase inhibitor belonging to the antimetabolite class of cytotoxic drugs. It is also effective in colorectal cancer (CRC) both as a single agent and in combination with other drugs, in particular in those patients with cardiologic risk factors or previous cardiotoxicity. The efficacy of first-line raltitrexed-based chemotherapy containing oxaliplatin (TOMOX) and irinotecan (TOMIRI) was investigated in this systematic review. Studies that enrolled advanced CRC patients for first-line therapy with TOMOX/ TOMIRI combinations were identified using electronic databases (Pubmed, SCOPUS, Web of Science, EMBASE, and the Cochrane Library). A systematic analysis was carried out using Comprehensive Meta Analysis (version 2.2.064) software to calculate the pooled response rate and 95% confidence limits. The median pooled overall survival and progression-free survival were also calculated. Results for TOMOX and TOMIRI studies were compared using the two-sided Student's t-test. We tested for significant heterogeneity using Cochran's chi(2)-test and I-2 index. Twelve studies published between 2001 and 2012 were eligible for this analysis and a total of 735 patients were enrolled in these studies. The overall response rate was 40% (95% confidence interval 34-46%): 43.9% for TOMOX and 34.1% for TOMIRI arms. The weighted median overall survival and progression-free survival times were 14.6 and 6.7 months, respectively. Neutropenia and liver toxicity were more frequent with TOMOX, whereas neutropenia and diarrhea were more frequent with TOMIRI. However, compared with historical FOLFOX and FOLFIRI trials, raltitrexed-based doublets are associated with less neutropenia and gastrointestinal toxicity and uncommon cardiotoxicity. TOMOX and TOMIRI doublets are active as first-line chemotherapy for advanced CRC and seem useful in particular when the use of 5-fluorouracil is contraindicated for cardiac comorbidity. (C) 2014 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
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页码:1122 / 1128
页数:7
相关论文
共 35 条
[31]  
Shaib W, 2009, IN VIVO, V23, P821
[32]  
Thomas R., 2000, P AN M AM SOC CLIN, V19, p308a
[33]   FOLFIRI followed by FOLFOX6 or the reverse sequence in advanced colorectal cancer:: A randomized GERCOR study [J].
Tournigand, C ;
André, T ;
Achille, E ;
Lledo, G ;
Flesh, M ;
Mery-Mignard, D ;
Quinaux, E ;
Couteau, C ;
Buyse, M ;
Ganem, G ;
Landi, B ;
Colin, P ;
Louvet, C ;
de Gramont, A .
JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (02) :229-237
[34]   Cetuximab and Chemotherapy as Initial Treatment for Metastatic Colorectal Cancer [J].
Van Cutsem, Eric ;
Koehne, Claus-Henning ;
Hitre, Erika ;
Zaluski, Jerzy ;
Chien, Chung-Rong Chang ;
Makhson, Anatoly ;
D'Haens, Geert ;
Pinter, Tamas ;
Lim, Robert ;
Bodoky, Gyoergy ;
Roh, Jae Kyung ;
Folprecht, Gunnar ;
Ruff, Paul ;
Stroh, Christopher ;
Tejpar, Sabine ;
Schlichting, Michael ;
Nippgen, Johannes ;
Rougier, Philippe .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 360 (14) :1408-1417
[35]   Adjuvant therapy with raltitrexed in patients with colorectal cancer intolerant of 5-fluorouracil: British Columbia cancer agency experience [J].
Wilson, Kenneth S. ;
Fitzgerald, Catherine A. ;
Barnett, Jeff B. ;
Gill, Sharlene ;
Khoo, Kong E. .
CANCER INVESTIGATION, 2007, 25 (08) :711-714