First-Line Cetuximab Plus Capecitabine in Elderly Patients with Advanced Colorectal Cancer: Clinical Outcome and Subgroup Analysis According to KRAS Status from a Spanish TTD Group Study

被引:58
|
作者
Sastre, Javier [1 ,2 ]
Gravalos, Cristina [3 ]
Rivera, Fernando [4 ]
Massuti, Bartomeu [5 ]
Valladares-Ayerbes, Manuel [6 ]
Marcuello, Eugenio [7 ]
Manzano, Jose L. [8 ]
Benavides, Manuel [9 ]
Hidalgo, Manuel [10 ]
Diaz-Rubio, Eduardo
Aranda, Enrique [11 ]
机构
[1] Hosp Clin San Carlos, Dept Med Oncol, Madrid 28040, Spain
[2] Spanish Minist Sci & Innovat, Inst Carlos 3, Ctr Red Temat Invest Cooperat Rd06 0020 0021, Madrid, Spain
[3] Hosp 12 Octubre, E-28041 Madrid, Spain
[4] Hosp Marques de Valdecilla, Santander, Spain
[5] Hosp Gen Alicante, Alicante, Spain
[6] Complejo Hosp Univ, La Coruna, Spain
[7] Hosp Santa Creu & Sant Pau, Barcelona, Spain
[8] Hosp Badalona Germans Trias & Pujol, Badalona, Spain
[9] Hosp Carlos Haya, Malaga, Spain
[10] Ctr Oncol Clara Campal, Madrid, Spain
[11] Hosp Reina Sofia, Cordoba, Spain
关键词
Capecitabine; Cetuximab; Colorectal neoplasms; Aged patients; RANDOMIZED CONTROLLED-TRIAL; PHASE-III TRIALS; COMBINATION CHEMOTHERAPY; COOPERATIVE GROUP; LOW TOXICITY; IRINOTECAN; OXALIPLATIN; EFFICACY; LEUCOVORIN; SURVIVAL;
D O I
10.1634/theoncologist.2011-0406
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Single-agent cetuximab is safe and active in elderly patients with advanced colorectal cancer (CRC). A cetuximab-capecitabine combination has not previously been tested in elderly patients with advanced CRC. Material and Methods. Sixty-six patients with advanced CRC were treated with cetuximab as a 400 mg/m(2) i.v. infusion followed by 250 mg/m(2) i.v. weekly plus capecitabine at a dose of 1,250 mg/m(2) every 12 hours. After the inclusion of 27 patients, the protocol was amended for safety reasons, reducing the dose of capecitabine to 1,000 mg/m(2) every 12 hours. Thirty-nine additional patients were treated with the reduced dose of capecitabine. Results. The overall response rate was 31.8%. KRAS status was determined in 58 patients (88%). Fourteen of 29 patients with wild-type KRAS tumors responded (48.3%; 95% confidence interval [CI], 29.4%-67.5%), compared with six of 29 patients with mutant KRAS tumors (20.7%; 95% CI, 8.0%-39.7%). The median progression-free survival (PFS) interval was 7.1 months. The median PFS interval for patients whose tumors were wild-type KRAS was significantly longer than for those with mutant KRAS tumors (8.4 months versus 6.0 months; p = .024). The high incidence of severe paronychia (29.6%) declined (7.7%) after capecitabine dose adjustment. Conclusions. Cetuximab plus capecitabine at a dose of 1,000 mg/m(2) every 12 hours may be an alternative to more aggressive regimens in elderly patients with advanced wild-type KRAS CRC. The Oncologist 2012; 17: 339-345
引用
收藏
页码:339 / 345
页数:7
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