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[转移性结直肠癌的抗血管生成治疗:持续的血管生成阻断是否合理?]

[Anti-angiogenic treatments in metastatic colorectal cancer: Does a continuous angiogenic blockade make sense?].

作者信息

Jary Marine, Borg Christophe, Bouché Olivier, Kim Stéfano, André Thierry, Bennouna Jaafar

机构信息

CHRU de Besançon, IRFC, service d'oncologie médicale, 25000 Besançon, France.

CHRU de Besançon, IRFC, service d'oncologie médicale, 25000 Besançon, France; Unité Inserm 1098, université de Franche-Comté, 25000 Besançon, France.

出版信息

Bull Cancer. 2015 Sep;102(9):758-71. doi: 10.1016/j.bulcan.2015.05.002. Epub 2015 Jul 29.

Abstract

Ten years after the approval of bevacizumab in colorectal cancer patients, results from ML18147 and CORRECT studies have recently demonstrated the possibility to target angiogenesis in patients previously exposed to anti-VEGF. An increasing number of anti-angiogenic treatments are now available, however, no biomarker has yet succeeded in rationalizing our therapeutic strategies. Nevertheless, several lessons have been learned from preclinical and pivotal clinical studies. The first clinical trials demonstrated a survival benefit, adding VEGFA targeting monoclonal antibodies to chemotherapy in metastatic colorectal cancer patients (AVF2107, ECOG 3200). Many phase III clinical trials confirmed the interest of this strategy, in combination with chemotherapies containing irinotecan, oxaliplatin, or with 5-fluorouracil in monotherapy. To date, such results have not been reproduced with tyrosine kinase inhibitors targeting the angiogenesis pathways, with an increasing rate of chemotherapy related toxicities. Clinical trials performed in the adjuvant setting (AVANT, NSABPC08) failed to demonstrate any efficacy of the anti-VEGFA treatments on the micrometastatic disease, encouraging its prescription in the unresectable cases. On the other hand, a continuous inhibition of angiogenesis during the course of the metastatic disease was shown to be feasible and to extend colon cancer patient's survival in two recent randomized trials. For these patients, the continuation of bevacizumab beyond progression in first line improves overall survival. Lastly, results achieved by the CORRECT and CONCUR studies demonstrated that anti-angiogenics might be effective in colorectal cancers resistant to chemotherapy. This review presents the main results of preclinical and clinical studies sustaining the prescription of anti-angiogenics in metastatic colorectal cancers. The future challenge is to promote the development of biomarkers to enable the stratification of the different therapeutic strategies.

摘要

贝伐单抗获批用于治疗结直肠癌患者十年后,ML18147和CORRECT研究的结果最近表明,在先前接受过抗VEGF治疗的患者中靶向血管生成是可行的。目前有越来越多的抗血管生成治疗方法,但尚未有生物标志物能够成功地使我们的治疗策略合理化。尽管如此,从临床前和关键临床研究中还是吸取了一些经验教训。首批临床试验显示了生存获益,在转移性结直肠癌患者中(AVF2107,ECOG 3200),将靶向VEGFA的单克隆抗体添加到化疗中。许多III期临床试验证实了该策略的益处,该策略可与含伊立替康、奥沙利铂的化疗联合使用,或与单药5-氟尿嘧啶联合使用。迄今为止,靶向血管生成途径的酪氨酸激酶抑制剂尚未再现此类结果,且化疗相关毒性发生率不断增加。在辅助治疗环境中进行的临床试验(AVANT,NSABPC08)未能证明抗VEGFA治疗对微转移疾病有任何疗效,这促使其在不可切除病例中使用。另一方面,在两项近期的随机试验中,显示在转移性疾病过程中持续抑制血管生成是可行的,并可延长结肠癌患者的生存期。对于这些患者,一线治疗进展后继续使用贝伐单抗可改善总生存期。最后,CORRECT和CONCUR研究取得的结果表明,抗血管生成药物可能对化疗耐药的结直肠癌有效。本综述介绍了支持在转移性结直肠癌中使用抗血管生成药物的临床前和临床研究的主要结果。未来的挑战是促进生物标志物的开发,以实现不同治疗策略的分层。

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