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西妥昔单抗联合化疗方案治疗晚期结直肠癌的临床疗效 被引量:7

Clinical investigation of cetuximab treatment combined with radio- and chemotherapy in advanced colorectal cancer patients
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摘要 目的评价西妥昔单抗联合化疗方案治疗晚期结直肠癌的疗效及不良反应。方法选择我院2007年1月-2010年6月单用或联合化疗使用西妥昔单抗治疗晚期或转移性结直肠癌患者35例,采用RF,cISr 1.1版实体肿瘤客观疗效评定标准进行临床疗效评价。并采用美国毒性反应评价标准(CIE 3.0)进行不良反应评价。结果共有31例纳入疗效评价。其中完全缓解l例,部分缓解9例,疾病稳定14例,疾病进展7例,有效率32.3%,疾病控制率75.O%;K-RAS基因野生型的患者有效率(40.0%)明显高于未检测组(18.2%)。33例发生了不良反应,发生率94.3%,主要为I~Ⅱ级(占74.1%)。结论西妥昔单抗联合放化疗方案治疗晚期结直肠癌可获得较高有效率,延长了疾病进展时间。 AIM To investigate the response and adverse drug reactions of cetuximab treatment combined with raclio- and cberno- therapy in advanced colorectal cancer patients. METHODS From Jan. 2007 to Jun. 2010, clinical data of 35 patients with advanced or metastatic colorectal cancer treated by cetuximab singly or by cetuximab combined with chemotherapy were analyzed. The clinical curative effect and adverse drug reactions as well as the effective response rate of patients with wild-type K-RAS were studied. RESULTS There,was one patient reached complete response (CR), 9 patients reached partial response(PB), 14 patients were in stable condition (SC), and the 7 patients were disease progression (DP). The effective response rate was 32.3%, disease control rate(DCB) was 75.0%. The effective response rate(40.0% )of patients with wild-type K-RAS was better than untested group( 18.2% ). The adverse effect incidence rate was 94.3%, and I - II grade adverse drug reactions happened most frequently which accounted for 74.1%. CONCLUSION The effective response rate of cetuximab treatment combined with radio- and chemotherapy in advanced colorectal cancer patients is pretty high, and the combination treatment which prolonged the time-to-progression (1TP) and is worthy of clinical application.
出处 《中国临床药学杂志》 CAS 2012年第2期99-102,共4页 Chinese Journal of Clinical Pharmacy
关键词 靶向治疗 西妥昔单抗 药物不良反应 targeted therapy cetuximab adverse drug reaction
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参考文献8

  • 1刘慧龙,徐建明.EGFR单抗治疗结直肠癌研究进展[J].临床肿瘤学杂志,2008,13(10):948-953. 被引量:8
  • 2Cunningham D, Humblet Y, Siena S, et al. Cetuximab monotherapy and cetu~mab plus irinotecan in irinotecan-rdractm-y metastatic coloectal cancer[J] .N Engl Jmed,2004,351(4):337.
  • 3王洁.EGFRI相关皮肤不良反应中国临床治疗指导原则[N].中国医学论坛报,2008-04-03(B5).
  • 4叶煌阳,张映红,陈建清,陈培臻,林建清,庞红霞,孙龙,李晓虹,陈莉林.西妥昔单抗联合化疗在晚期结直肠癌一线治疗中的疗效观察[J].中国癌症杂志,2008,18(9):704-706. 被引量:6
  • 5Tabemero J, Pfeiffer P, Cervantes A. Administration of cetuximab every weeks in the tieatngnt d metastatic colorectal cancear: an effective,more convenient altemative to weekly administration[ J]. Oncologist,2008,13(2):113.
  • 6李瑾昱,焦顺昌.西妥昔单抗疗效预测指标的研究进展[J].现代肿瘤医学,2010,18(5):1026-1028. 被引量:5
  • 7Benvenuti S, Sartol-Bianchi A, Di Nicolantonio F, et al. Oncogc activation d the RAS/RAF signaling pathway impeh the response dmetastatic colorectal can to anti- epidermal growth factor Rcepto an-mmpies[J]. Crleer Res, 2007,67(6):2643.
  • 8Lievre A, Bachet JB, Boige V, et -1. KRAS nmtations as an indepen- dent prognostic factor in patients with advanced colorectal cancer treated with cettvdmeb[J]. J Clin Oncol,2008,26(3) :374.

二级参考文献60

  • 1Cunningham D, Humblet Y, Siena S, et al. Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer[ J]. N Engl J Med, 2004,351(4) :337 - 345.
  • 2Wilke H, Glynne-Jones R, Thaler J, et al. MABEL-A large multinational study of cetuximab plus irinotecan in irinotecan resistant metastatic colorectal cancer [ J ]. J Clin Oncol, 24 (18 Suppl ) :3549.
  • 3Lenz H J, Van Cutsem E, Khambata-Ford S, et al. Multicenter phase Ⅱ and translational study of cetuximab in metastatic colorectal carcinoma refractory to irinotecan, oxaliplatin, and fluoropyrimidines[ J]. J Clin Oncol, 2006,24(30) :4914 -4921.
  • 4Jonker D J, O'Callaghan C J, Karapetis CS, et al. Cetuximab for the treatment of colorectal cancer[ J]. N Engl J Med, 2007,357 (20) :2040-2048.
  • 5Saltz LB, Lenz HJ, Kindler HL, et al. Randomized phase Ⅱ trial of cetuximab, bevacizumab, and irinotecan compared with cetuximab and bevacizumab alone in irinotecan-refractory colorectal cancer: the BOND-2 study[J]. J Clin Oncol, 2007,25(29) : 4557 -4561.
  • 6Hecht JR, Patnaik A, Berlin J,et al. Panitumumab monotherapy in patients with previously treated metastatic colorectal cancer [J]. Cancer, 2007,110(5) :980 -988.
  • 7Van Cutsem E, Peeters M,Siena S,et al. Open-label phase Ⅲ trial of panitumumab plus best supportive care compared with best supportive care alone in patients with chemotherapy-refractory metastatic colorectal cancer[ J]. J Clin Oncot, 2007,25 (13) :1658 -1664.
  • 8Sobrero AF, Fehrenbacher L, Rivera F, et al. Randomized phase Ⅲ trial of cetuximab plus irinotecan vs. irinotecan alone for metastatic colorectal cancer in 1298 patients who have failed prior oxaliplatin-based therapy : The EPIC trial [ J/OL ]. 2007 [ 2008 - 3 -15]. http://www, medscape, com/viewarticle1560219.
  • 9Jennis A, Polikoff J, Mitchell E, et al. Erbitux (cetuximab) plus FOLFOX for colorectal cancer ( EXPLORE ) : preliminary efficacy analysis of a randomized phase Ⅲ trial[ J]. J Clin Oncol, 2005,23( 16 Suppl) :3574.
  • 10Souglakos J, Kalykaki A, Vamvakas L, et al. Phase Ⅱ trial of capecitabine and oxaliplatin (CAPOX) plus cetuximab in patients with metastatic colorectal cancer who progressed after oxali- platin-based chemotherapy [ J ]. Ann Oncol, 2007,18 ( 2 ) :305 - 310.

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