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西妥昔单抗联合化疗治疗转移性结直肠癌的临床观察 被引量:3

A Clinical Observation of Cetuximab Combined with Chemotherapy for Metastatic Colorectal Cancer Patients
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摘要 目的:观察西妥昔单抗联合FOLFIRI或FOLFOX方案治疗转移性结直肠癌的近期疗效及毒副反应。方法:2006年11月至2009年1月,我院收治的12例转移性结直肠癌患者,接受西妥昔单抗联合化疗治疗,西妥昔单抗首次给予负荷剂量400mg/m^2,而后每周维持量为250mg/m^2。有7例联合FOLFIRI方案,4例联合FOLFOX方案,1例联合奥沙利铂+放疗。分别按照RECIST标准和NCI-CTC 3.0评价疗效和毒性。结果:全组12例均可评价疗效,.PR 7例,SD 3例,PD 2例,总有效率58.3%,疾病控制率83.3%。疾病进展时间(TTP)1.5个月~15个月。主要毒副反应为痤疮样皮疹和腹泻。结论:西妥昔单抗联合FOLFIRI或FOLFOX方案治疗转移性结直肠癌安全有效,除痤疮样皮疹外,毒副作用无明显增加。 Objective: To observe the efficacy and toxicity of cetuximab plus chemotherapy containing irinotecan or oxaliplatin in the treatment of metastatic colorectal cancer. Methods: From November 2006 to January 2009,12 patients with metastatic colorectal cancer histologically confirmed were treated with cetuximab combined with chemotherapy containing irinotecan or oxaliplatin regimen. Cetuximab was given at an initial dose of 400mg/m^2, followed by weekly infusions of 250mg/m^2, including 7 patients combined with FOLFIRI regimen,4 patients combined with FOLFOX regimen and 1 patient combined with oxaliplatin regimen and radiotherapy. The efficacy and toxicity were evaluated according to RECIST and NCI-CTC 3.0 criteria. Results: The effects could be observed in 12 patients. 7 patients got PR, 3 patients SD and 2 patients PD, with the response rate of 58.3% and the disease control-rate of 83.3 %. The time to progression (TIP) was 1.5 -15 months. The major toxicities were none-like rash and diarrhea. Conclusion: Cetuximab combined with the chemotherapy containing irlnotecan or oxaliplatin has clinical efficacy in patients with metastatic colorectal cancer. No more toxicities, except rash, are observed in the patients receiving cetuximab combined with chemotherapy than chemotherapy alone.
出处 《肿瘤预防与治疗》 2010年第4期286-290,共5页 Journal of Cancer Control And Treatment
关键词 转移性结直肠癌 西妥昔单抗 伊立替康 奥沙利铂 Metastatic Coloreetal Cancer Cetuximab Irinotecan Oxaliplatin
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参考文献13

  • 1Tournigand C,André T,Achille E,et al.FOLFIRI followed by FOLFOX6 or the reverse sequence in advanced colorectal cancer:a randomized GERCOR study[J].J Clin Oncol,2004,22(2):229-237.
  • 2Prewett MC,Hooper AT,Bassi R,et al.Enhanced antitumor activity of anti-epidermal growth factor receptor monoclonal antibody IMC-C225 in combination with irinotecan (CPT-11) against human colorectal tumor xenografts[J].Clin Cancer Res,2002,8(5):994-1003.
  • 3Saltz LB,Meropol NJ,Loehrer PJ Sr,et al.Phase Ⅱ trial of cetuximab in patients with refractory colorectal cancer that expresses the epidermal growth factor receptor[J].J Clin Oncol,2004,22(7):1201-1208.
  • 4Cunningham 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.
  • 5Tabermero J,Van Cutsem E,Díaz-Rubio E,et al.Phase Ⅱtrial of cetuximab in combina-tion with fluorouracil,leucovorin,and oxaliplatin in the first-line treatment of metastatic colorectal cancer[J].J Clin Oncol,2007,25(33):5225-5232.
  • 6Van Cutsem E,Nowacki M,Lang L,et al.Randomized phase Ⅲ study of irinotecan and 5-FU /FA with or without cetuximab in the first-line treatment of patients with metastatic colo-rectal cancer(mCRC):The CRYSTAL trial[J].J Clin Oncol,2007,25(16s):4000.
  • 7Chung KY,Shia J,Kemeny NE,et al.Cetuximab shows activity in colorectal cancer patients with tumors that do not express the epidermal growth factor receptor by immunohistochemistry[J].J Clin Oncol,2005,23(9):1803-1810.
  • 8Van Cutsem E,Lang L,D'Haens G,et al.K-ras status and efficacy in the first-line treat ment of patients with metastatic colorectal cancer (mCRC) treated with FOLFIRI with or without cetuximab:The CRYSTAL experience[J].J Clin Oncol,2008,26(Supp l):abstr 2.
  • 9Tejpar S,Peeters M,Humblet Y,et al.Relationship of efficacy with K-ras status (wild type versus mutant) in patients with irinotecan-refractory metastatic colorectal cancer (mCRC),treated with irinotecan (q2w) and escalating doses of cetuximab(q1w):The EVEREST experince (preliminary date)[J].J Clin Oncol,2008,26(Supp l):abstr 4001.
  • 10徐建明,张华.西妥昔单抗单药或与伊立替康联合治疗伊立替康耐药的转移性结直肠癌[J].循证医学,2006,6(5):274-276. 被引量:14

二级参考文献16

  • 1钱军,秦叔逵,曹梦苒,邵志坚,成远,吴成利.西妥昔单抗联合伊立替康为主方案治疗耐药性晚期结直肠癌的临床观察[J].中国癌症杂志,2007,17(1):29-31. 被引量:6
  • 2De Gramont A, Figer A, Seymour M, et al. Leucovorin and fluorouracil with or without oxaliplatin as first-line treatment in advanced colorectal cancer [J]. J Clin Oncol, 2000, 18:2938-2947.
  • 3Douillard JY, Cunningham D, Roth AD, et al. Irinotecan combined with fluorouracil compared with fluorouracil alone as first-line treatment for metastatic colorectal cancer: a multicentre randomized trial [J]. Lancet, 2000,355:1041-1047.
  • 4Herbst RS, Shin DM. Monoclonal antibodies to target epidermal growth factor receptor positive tumors:a new paradigm for cancer therapy [J]. Cancer, 2002,94: 1593-1611.
  • 5Hurwitz H, Fehrenbacher L, Novotny W, et al. Bevacizumab plus irinitecan, fluorouracil, and leucovorin for metastatic colorectal cancer [J]. N Engl J Med, 2004,350:2335-2342.
  • 6Lievre A, bachet JB, Le Corre D, et al. KRAS mutation status is predictive of response to cetuximab therapy in colorectal cancer [J]. Cancer Res, 2006,66: 3992-3995.
  • 7Moroni M, Veronese S, Benvenuti S, et al. Gene copy number for epidermal growth factor receptor (EGFR) and clinical response to antiEGFR treatment in colorectal cancer:a cohort study [J]. Lancet Oncol, 2005,6: 279-286.
  • 8Saltz LB, Meropol N J, Loehrer PJ Sr, et al. Phase Ⅱ trial of cetuximab in patients with refractory colorectal cancer that expresses the epidermal growth factor receptor [ J ]. J Clin Oncol, 2004,22 : 1201-1208.
  • 9Cunningham D, Humblet Y, Siena S, et al. Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer[J]. N Engl J Med, 2004,351:337-345.
  • 10Lenz HJ, 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, 2006,24:4914-4921.

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