Efficacy and Safety of Raltitrexed Combinations with Uracil-Tegafur or Mitomycin C as Salvage Treatment in Advanced Colorectal Cancer Patients: A Multicenter Study of Anatolian Society of Medical Oncology (ASMO)

被引:7
|
作者
Bozkurt, Oktay [1 ]
Karaca, Halit [1 ]
Ciltas, Aydin [2 ]
Kaplan, M. Ali [3 ]
Benekli, Mustafa [2 ]
Sevinc, Alper [4 ]
Demirci, Umut [5 ]
Eren, Tulay [6 ]
Kodaz, Hilmi [7 ]
Isikdogan, Abdurrahman [3 ]
Ozkan, Metin [1 ]
Buyukberber, Suleyman [2 ]
机构
[1] Erciyes Univ, Dept Med Oncol, Fac Med, Kayseri, Turkey
[2] Gazi Univ, Dept Med Oncol, Fac Med, Ankara, Turkey
[3] Dicle Univ, Dept Med Oncol, Fac Med, Diyarbakir, Turkey
[4] Gaziantep Univ, Dept Med Oncol, Fac Med, Gaziantep, Turkey
[5] Ankara Ataturk Res & Teaching Hosp, Ankara, Turkey
[6] Ankara Numune Res & Teaching Hosp, Ankara, Turkey
[7] Trakya Univ, Dept Med Oncol, Fac Med, Trakya, Turkey
关键词
Raltitrexed; uracil-tegafur; mitomycin C; salvage treatment; colorectal cancer; 3RD-LINE CHEMOTHERAPY; RANDOMIZED-TRIAL; ORAL LEUCOVORIN; PHASE-III; FLUOROURACIL; IRINOTECAN; 5-FLUOROURACIL; THERAPY; TOMUDEX; 5-FU;
D O I
10.7314/APJCP.2014.15.4.1845
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: There is no standard treatment for patients with colorectal cancer (CRC) progressing after irinotecan and oxaliplatin treatment. Here we aimed to retrospectively evaluate the efficacy and tolerability of raltitrexed in combination with oral 5-fluoropyrimidine (uracil tegafur-UFT) or mitomycin C as salvage therapy in mCRC patients. Materials and Methods: A total of 62 patients who had received raltitrexed combined with UFT or mitomycin C were identified between December 2008 and June 2013. They were given raltitrexed 2.6 mg/m(2) (max 5 mg) i.v. on day 1 in combination with either oral UFT 500 mg/day on days 1-14 every 3 weeks (group A) or mitomycin C 6 mg/m(2) i.v. on day every 3 weeks (group B). Results: Forty-two patients (67.7%) were in group A and 20 (32.2%) in group B. In 15 patients (24%) grade 3/4 toxicity was observed, resulting in dose reduction, and in 13 patients (20.9%) dose delay was necessary. The median progression free survival (PFS) was 3 months (95% CI 2.65-3.34) and median overall survival (OS) was 6 months (95% CI 2.09-9.90) in the whole group. Median PFS was 3 months (95% CI 2.60-3.39) in group A vs 3 months (95% CI 1.64-4.35) in group B (p=0.90). Median OS was 6 months (95% CI 2.47-9.53) in group A vs 12 months (95% CI 2.83-21.1) in group B (p=0.46). Conclusions: The combination of raltitrexed with UFT or mitomycin C seem to be a salvage therapy option due to safety profile and moderate clinical activity in heavily-pretreated mCRC patients.
引用
收藏
页码:1845 / 1849
页数:5
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