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
[1]   First-line treatment with irinotecan and raltitrexed in metastatic colorectal cancer -: Mature results of a multicenter phase II study [J].
Aparicio, J ;
Vicent, JM ;
Maestu, I ;
Bosch, C ;
Galán, A ;
Busquier, I ;
Llorca, C ;
Garcerá, S ;
Campos, JM ;
López-Tendero, P ;
Balcells, M .
ONCOLOGY, 2005, 68 (01) :58-63
[2]   Multicenter phase II trial evaluating a three-weekly schedule of irinotecan plus raltitrexed in patients with 5-fluorouracil-refractory advanced colorectal cancer [J].
Aparicio, J ;
Vicent, JM ;
Maestu, I ;
Garcerá, S ;
Busquier, I ;
Bosch, C ;
Llorca, C ;
Díaz, R ;
Fernández-Martos, C ;
Galán, A .
ANNALS OF ONCOLOGY, 2003, 14 (07) :1121-1125
[3]   Targeting thymidylate synthase in colorectal cancer: critical re-evaluation and emerging therapeutic role of raltitrexed [J].
Avallone, Antonio ;
Di Gennaro, Elena ;
Silvestro, Lucrezia ;
Iaffaioli, Vincenzo Rosario ;
Budillon, Alfredo .
EXPERT OPINION ON DRUG SAFETY, 2014, 13 (01) :113-129
[4]   Cardiotoxicity of the antiproliferative compound fluorouracil [J].
Becker, K ;
Erckenbrecht, JF ;
Häussinger, D ;
Frieling, T .
DRUGS, 1999, 57 (04) :475-484
[5]   Irinotecan and raltitrexed: an active combination in advanced colorectal cancer [J].
Carnaghi, C ;
Rimassa, L ;
Garassino, I ;
Zucali, PA ;
Masci, G ;
Fallini, M ;
Morenghi, E ;
Santoro, A .
ANNALS OF ONCOLOGY, 2002, 13 (09) :1424-1429
[6]   Dosing Considerations for Capecitabine-Irinotecan Regimens in the Treatment of Metastatic and/or Locally Advanced Colorectal Cancer [J].
Cartwright, Thomas ;
McCollum, David ;
Boehm, Kristi A. .
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2010, 33 (03) :307-313
[7]   Raltitrexed plus oxaliplatin (TOMOX) as first-line chemotherapy for metastatic colorectal cancer.: A phase II study of the Italian Group for the Study of Gastrointestinal Tract Carcinomas (GISCAD) [J].
Cascinu, S ;
Graziano, F ;
Ferraù, F ;
Catalano, V ;
Massacesi, C ;
Santini, D ;
Silva, RR ;
Barni, S ;
Zaniboni, A ;
Battelli, N ;
Siena, S ;
Giordani, P ;
Mari, D ;
Baldelli, AM ;
Antognoli, S ;
Maisano, R ;
Priolo, D ;
Pessi, MA ;
Tonini, G ;
Rota, S ;
Labianca, R .
ANNALS OF ONCOLOGY, 2002, 13 (05) :716-720
[8]  
Chiara S, 2005, ANTICANCER RES, V25, P1391
[9]   'Tomudex' (ZD1694): Results of a randomised trial in advanced colorectal cancer demonstrate efficacy and reduced mucositis and leucopenia [J].
Cunningham, D ;
Zalcberg, JR ;
Rath, U ;
Olver, I ;
VanCutsem, E ;
Svensson, C ;
Seitz, JF ;
Harper, P ;
Kerr, D ;
PerezManga, G ;
Azab, M ;
Seymour, L ;
Lowery, K ;
Ackland, SP ;
Basser, RL ;
Clarke, SJ ;
Goldstein, D ;
Green, MD ;
Grygiel, JJ ;
McKendrick, JJ ;
Millward, MJ ;
Olver, IN ;
Tattersall, MHN ;
Thomson, DB ;
Jakesz, R ;
Buset, M ;
Tueni, EA ;
VanCutsem, EJD ;
Bauer, J ;
Beska, F ;
Adenis, A ;
Brunet, R ;
Francois, E ;
Paillot, B ;
Rougier, P ;
Fink, UFW ;
Knuth, KRA ;
Koenig, HJ ;
Bohme, MWJ ;
Wander, HE ;
Amadori, D ;
Frassineti, L ;
Cocconi, G ;
Passalacqua, R ;
Frigerio, F ;
Barni, S ;
Luporini, G ;
Labianca, R ;
Marini, G ;
Zaniboni, A .
EUROPEAN JOURNAL OF CANCER, 1995, 31A (12) :1945-1954
[10]   Efficacy, tolerability and management of raltitrexed (Tomudex™) monotherapy in patients with advanced colorectal cancer:: a review of phase II/III trials [J].
Cunningham, D ;
Zalcberg, J ;
Maroun, J ;
James, R ;
Clarke, S ;
Maughan, TS ;
Vincent, M ;
Schulz, J ;
Barón, MG ;
Facchini, T .
EUROPEAN JOURNAL OF CANCER, 2002, 38 (04) :478-486