KRAS Mutation Status and Clinical Outcome of Preoperative Chemoradiation With Cetuximab in Locally Advanced Rectal Cancer: A Pooled Analysis of 2 Phase II Trials

被引:29
|
作者
Kim, Sun Young [1 ]
Shim, Eun Kyung [1 ]
Yeo, Hyun Yang [2 ]
Baek, Ji Yeon [1 ]
Hong, Yong Sang [3 ]
Kim, Dae Yong [1 ,2 ]
Kim, Tae Won [3 ]
Kim, Jee Hyun [4 ]
Im, Seock-Ah [5 ]
Jung, Kyung Hae [3 ]
Chang, Hee Jin [1 ,2 ]
机构
[1] Natl Canc Ctr, Res Inst & Hosp, Ctr Colorectal Canc, Goyang, Gyeonggi Do, South Korea
[2] Natl Canc Ctr, Res Inst & Hosp, Div Translat & Clin Res 1, Goyang, Gyeonggi Do, South Korea
[3] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Oncol, Seoul, South Korea
[4] Seoul Natl Univ, Bundang Hosp, Coll Med, Dept Internal Med, Songnam, South Korea
[5] Seoul Natl Univ, Coll Med, Seoul Natl Univ Hosp, Dept Internal Med, Seoul, South Korea
关键词
GROWTH-FACTOR RECEPTOR; PLUS IRINOTECAN; PRIMARY TUMORS; PTEN; CAPECITABINE; INTEGRATION; METASTASES; INHIBITORS; EXPRESSION; THERAPY;
D O I
10.1016/j.ijrobp.2012.03.048
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Cetuximab-containing chemotherapy is known to be effective for KRAS wild-type metastatic colorectal cancer; however, it is not clear whether cetuximab-based preoperative chemoradiation confers an additional benefit compared with chemoradiation without cetuximab in patients with locally advanced rectal cancer. Methods and Materials: We analyzed EGFR, KRAS, BRAF, and PIK3CA mutation status with direct sequencing and epidermal growth factor receptor (EGFR) and Phosphatase and tensin homolog (PTEN) expression status with immunohistochemistry in tumor samples of 82 patients with locally advanced rectal cancer who were enrolled in the IRIX trial (preoperative chemoradiation with irinotecan and capecitabine; n=44) or the ERBIRIX trial (preoperative chemoradiation with irinotecan and capecitabine plus cetuximab; n=38). Both trials were similarly designed except for the administration of cetuximab; radiation therapy was administered at a dose of 50.4 Gy/28 fractions and irinotecan and capecitabine were given at doses of 40 mg/m(2) weekly and 1650 mg/m(2)/day, respectively, for 5 days per week. In the ERBIRIX trial, cetuximab was additionally given with a loading dose of 400 mg/m(2) on 1 week before radiation, and 250 mg/m(2) weekly thereafter. Results: Baseline characteristics before chemoradiation were similar between the 2 trial cohorts. A KRAS mutation in codon 12, 13, and 61 was noted in 15 (34%) patients in the IRIX cohort and 5 (13%) in the ERBIRIX cohort (P=.028). Among 62 KRAS wild-type cancer patients, major pathologic response rate, disease-free survival and pathologic stage did not differ significantly between the 2 cohorts. No mutations were detected in BRAF exon 11 and 15, PIK3CA exon 9 and 20, or EGFR exon 18-24 in any of the 82 patients, and PTEN and EGFR expression were not predictive of clinical outcome. Conclusions: In patients with KRAS wild-type locally advanced rectal cancer, the addition of cetuximab to the chemoradiation with irinotecan plus capecitabine regimen was not associated with improved clinical outcome compared with chemoradiation without cetuximab. (C) 2013 Elsevier Inc.
引用
收藏
页码:201 / 207
页数:7
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