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西妥昔单抗联合mFOLFOX6一线治疗k-ras野生型结直肠癌肝转移临床疗效观察 被引量:9

Cetuximab plus mFOLFOX6 in k-ras wild–type patients with unresectable liver metastases from colorectal cancer
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摘要 目的评价西妥昔单抗联合mFOLFOX6一线治疗k-ras野生型结直肠癌肝转移患者的临床疗效及安全性。方法本院自2008年1月至2011年12月收治的失去手术机会的晚期结直肠癌肝转移患者39例,其中一线接受西妥昔单抗联合mFOLFOX6方案治疗19例(联合组),单用mFOLFOX6方案化疗20例(化疗组),具体方案为:西妥昔单抗首次400 mg/m2,静脉滴注120 min,后续每周250 mg/m2,静脉滴注60 min,每周给药1次或500 mg/m2,首次静脉滴注120 min,之后每次滴注60 min,每2周给药1次;mFOLFOX6方案:奥沙利铂85 mg/m2,第1天,LV 400 mg/m2,第1天,5-FU 400 mg/m2,静推,第1天,2400 mg/m2,持续静注46 h,2周为一周期;化疗组仅接受上述mFOLFOX6方案化疗。结果全组39例患者均可评价疗效,联合组获得CR 2例(10.5%),PR 11例(57.9%),SD 4例(21.1%),PD 2例(10.5%),RR为68.4%,DCR为89.5%。化疗组获得CR为0例,PR 6例(30.0%),SD 8例(40.0%),PD 6例(30.0%),RR为30.0%,DCR为70.0%。两组缓解率RR比较有统计学差异(P=0.016),中位PFS分别为10.4个月、6.3个月,联合组优于化疗组;获得R0肝转移灶切除者两组分别为36.8%vs.10.0%(P=0.047),手术者PFS分别为12.6个月、15.6个月,均优于未获得手术机会的患者;主要不良反应为皮疹、腹泻、恶心呕吐、神经毒性及血液学毒性,均可耐受。结论西妥昔单抗联合mFOLFOX6一线治疗k-ras野生型晚期结直肠癌肝转移患者,获得较好的临床缓解率及更高的肝切除率,获得R0肝转移灶切除的患者可以获得更高的疾病无进展时间,两组不良反应均可耐受,值得在临床推广应用。 Objective To assess the efficacy and adverse effects of cetuximab plus mFOLFOX6 as first-line treatment for K-Ras wild type patients with unresectable colorectal liver metastases. Methods From January 2008 to December 2011, 39 patients with unresectable liver metastases from k-ras wild-type colorectal cancer were assigned, while 19 patients were treated with cetuximab (500 mg/m2 iv ) biweekly plus mFOLFOX6 (L-OHP 100 mg/m2, leucovorin 400 mg/m2, 5-fluorouracil 400 mg/m2 bolus and 5-fluorou- racil 2400 mg/m2 46-hour infusion, biweekly) and 20 patients received mFOLFOX6 only. Results In two teams, RR was 57.9% vs. 30.0%, DCR was 84.2% vs. 70.0%, mPFS was 10.4 vs. 6.3 months; The liver resection rate was 26.3% (5/19) vs. 10.0% (2/20), the PFS was 12.6 and 15.6 months,longer than these who had no chance of resection. The common adverse events were skin rash, digestive reaction and neutropenia, mainly in grade 1-2. Conclusion Cetuximab plus mFOLFOX6 in k-ras wild-type patients with unresectable liver metastases from colorectal cancer is effective and the adverse effect is tolerate, worth further study.
出处 《中华临床医师杂志(电子版)》 CAS 2013年第19期41-43,共3页 Chinese Journal of Clinicians(Electronic Edition)
关键词 西妥昔单抗 结直肠肿瘤 肿瘤转移 K-RAS基因 药物疗法 Cetuximab Colorectal neoplasms Neoplasm metastasis K-Ras gene Drug therapy
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参考文献11

  • 1Tajima Y,Ishibashi K,Matsuzawa T. A long-term survivor of colorectal cancer associated with multiple liver metastases and peritoneal carcinomatosis treated through a multidisciplinary approach[J].Gan To Kagaku Ryoho,2012.2240-2242.
  • 2Ku GY,Haaland BA,de Lima Lopes G Jr. Cetuximab in the first-line treatment of K-ras wild-type metastatic colorectal cancer:the choice and schedule of fluoropyrimidine matters[J].Cancer Chemotherapy and Pharmacology,2012.231-238.
  • 3Ye LC,Liu TS,Ren L. Randomized Controlled Trial of Cetuximab Plus Chemotherapy for Patients With KRAS Wild-Type Unresectable Colorectal Liver-Limited Metastases[J].Journal of Clinical Oncology,2013.1931-1938.
  • 4Brodowicz T,Ciuleanu TE,Radosavljevic D. FOLFOX4 plus cetuximab administered weekly or every second week in the first-line treatment of patients with KRAS wild-type metastatic colorectal cancer:a randomized phase II CECOG study[J].ANNALS OF ONCOLOGY,2013.1769-1777.
  • 5Chibaudel B,Tournigand C,Andre T. Therapeutic strategy in unresectable metastatic colorectal cancer[J].Ther Adv Med Oncol,2012.75-89.
  • 6Modest DP,Laubender RP. Early tumor shrinkage in patients with metastatic colorectal cancer receiving first-line treatment with cetuximab combined with either CAPIRI or CAPOX:An analysis of the German AIO KRK 0104 trial[J].ACTA ONCOLOGICA,2013.956-962.
  • 7Jiang Z,Li C,Li F. EGFR gene copy number as a prognostic marker in colorectal cancer patients treated with cetuximab or panitumumab:asystematic review and meta analysis[J].PLoS One,2013.e56205.
  • 8Licitra L,St?rkel S,Kerr KM. Predictive value of epidermal growth factor receptor expression for first-line chemotherapy plus cetuximab in patients with head and neck and colorectal cancer:Analysis of data from the EXTREME and CRYSTAL studies[J].EUROPEAN JOURNAL OF CANCER,2013.1161-1168.
  • 9Saridaki Z,Androulakis N,Vardakis N. A triplet combination with irinotecan(CPT-11),oxaliplatin(LOHP),continuous infusion 5-fluorouracil and leucovorin(FOLFOXIRI)plus cetuximab as first-line treatment in KRAS wt,metastatic colorectal cancer:a pilot phase Ⅱ trial[J].British Journal of Cancer,2012.1932-1937.
  • 10Van Cutsem E,K?hne CH,Láng I. Cetuximab plus irinotecan,fluorouracil,and leucovorin as first-line treatment for metastatic colorectal cancer:updated analysis of overall survival according to tumor KRAS and BRAF mutation status[J].Journal of Clinical Oncology,2011.2011-2019.

同被引文献101

  • 1王磊,白喜玲,朱道奇.西妥昔单抗治疗胃肠道恶性肿瘤的临床疗效观察[J].中华结直肠疾病电子杂志,2014,3(3):22-25. 被引量:2
  • 2许剑民,钟芸诗,牛伟新,任黎,赖衍翰,王建华,颜志平,程洁敏,秦新裕.术前肝动脉联合区域动脉灌注化疗预防结直肠癌术后肝转移[J].中华医学杂志,2006,86(2):88-92. 被引量:20
  • 3腹腔镜结肠直肠癌根治手术操作指南(2006版)[J].外科理论与实践,2006,11(5):462-464. 被引量:271
  • 4庞丹梅,邓燕明,林耀东,徐绮华.mFOLFOX6方案用于进展期胃癌术后辅助化疗的临床研究[J].实用癌症杂志,2007,22(3):269-270. 被引量:10
  • 5Hernandez - Hernandez OT, Camacho - Arroyo I. Regulation of geneex- pression by progesterone in cancer cells: Effects on cyclin D1, EGFR and VEGF[J]. Mini Rev Med Chem, 2013,13 (5) : 635 - 642.
  • 6Bronte G, Cicero G, Cusenza S, eta|. Monoc|ona| antibodies ingastrointesti- nal cancers [ J ]. Expert Opin Biol Ther, 2013,13 (6) : 889 - 900.
  • 7Shuman ML, Jensen - Taubman S, Stetler - Stevenson WG. Matrixmetallo- proteinases: Changing roles in tumor progression and metastasis [J]. Am J Pathol, 2012,181 (6) : 1 895 - 1 899.
  • 8Gibson R.I, Keefe DM, Lalla RV, et al. Systematic review ofagents for the management of gastrointestinal mucositis in cancerpatients [J]. Support Care Cancer,2013,21 (1): 313 - 326.
  • 9Nordlinger B,Sorbye H,Glimelius B,et al.Perioperative FOLFOX4 chemotherapy and surgery versus surgery alone for resectable liver metastases from colorectal cancer(EORTC 40983):long-term results of a randomised,controlled,phase 3 trial[J].Lancet Oncol,2013,14:1208-1215.
  • 10Ychou M,Rivoire M,Thezenas S,et al.A randomized phaseⅡtrial of three intensified chemotherapy regimens in first-line treatment of colorectal cancer patients with initially unresectable or not optimally resectable liver metastases.The METHEP trial[J].Ann Surg Oncol,2013,20:4289-4297.

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