II期结肠癌患者的辅助化疗

H. J. Kim
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引用次数: 0

摘要

67结肠癌根治性切除术后辅助化疗的目的是根除微转移,减少复发率,提高总生存率。然而,化疗可能有副作用的风险,并降低生活质量。因此,在决定是否增加化疗时,应综合考虑复发风险与化疗风险之间的平衡。辅助化疗在III期结肠癌治疗中的优势已被大量随机对照试验充分证实,目前已被视为一种标准治疗方法[1]。对于方案,建议采用传统的5-氟尿嘧啶(5-FU)和亚叶酸钙,卡培他滨单药治疗,FOLFOX或CAPOX。然而,在II期结肠癌中,如果进行根治性切除,预后非常好,根治性切除后的总生存率约为80%[2,3]。辅助化疗在II期结肠癌中的作用很小,仍然是一个有很大争议的领域[4]。哪些患者会从辅助化疗中受益,以及使用何种化疗仍然是一个有很大争议的领域。因为II期结肠癌患者是一个异质性组合,包括IIA期(pT3N0)、IIB期(pT4aN0)和IIC期(pT4bN0)。目前的指南建议对有复发高危因素的II期结肠癌患者进行辅助化疗,如低分化组织学(不包括那些微卫星不稳定性高的癌症[MSI-H])、淋巴/血管浸润、肠梗阻、检查的< 12个淋巴结、神经周围浸润、局部穿孔或边缘闭合、不确定或阳性。对于奥沙利铂的添加,根据MOSAIC和NSABP C-07试验的亚组分析,在5- fu和亚叶酸蛋白的基础上添加奥沙利铂治疗II期结肠癌没有发现明显的获益[5,6]。因此,考虑到奥沙利铂潜在的副作用风险,包括神经病变,不建议在II期结肠癌患者中添加奥沙利铂。另一个应该考虑的因素是错配修复或MSI测试。由于MSI-H患者可能预后较好,5-FU辅助治疗效果不佳,因此应在确定II期结肠癌辅助化疗前进行检查[7]。作者试图找出哪些患者可以在II期结肠癌中省略辅助化疗。他们发现只有一种复发高危因素的患者通过辅助化疗可能没有明显的获益[8]。然而,我们应该谨慎解读,因为为了证明辅助化疗对II期结肠癌的潜在益处很小,不可避免地需要大量的人群。综上所述,考虑到以上所有因素,临床医生和患者之间关于辅助化疗对II期结肠癌的潜在风险和益处的对话对于决策非常重要。应该进行个性化治疗。韩国临床肿瘤杂志2018;14:67-68 https://doi.org/10.14216/kjco.18012 pISSN 1738-8082∙eISSN 2288-4084
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adjuvant chemotherapy in patients with stage II colon cancer
67 The purpose of adjuvant chemotherapy after curative resection of colon cancer is eradication of micrometastatic disease, decreasing the recurrence and improving the overall survival. However, chemotherapy may have risk of side effects, and decrease the quality of life. Therefore, the decision making to adding chemotherapy should be made under considering the balance between the risk of recurrence and chemotherapy. The advantage of adjuvant chemotherapy in stage III colon cancer is well proven by many randomized controlled trials and now it is regarded as a standard treatment [1]. As for the regimen, traditional 5-fluorouracil (5-FU) and leucovorin, capecitabine monotherapy, FOLFOX, or CAPOX are recommended. However, in stage II colon cancer, if the curative resection was performed, the prognosis is very good and the overall survival after curative resection is reported around 80% [2,3]. The role of adjuvant chemotherapy in stage II colon cancer is minimal and remains an area of great controversy [4]. And which patients will benefit from adjuvant chemotherapy and what chemotherapy to use also remain an area of great controversy. Because patients with stage II colon cancer comprise a heterogeneous combination including stage IIA (pT3N0), stage IIB (pT4aN0), and stage IIC (pT4bN0). Current guidelines recommend adjuvant chemotherapy for stage II colon cancer for the patient with high-risk factors for recurrence such as poorly differentiated histology (exclusive of those cancers that are high microsatellite instability [MSI-H]), lymphatic/vascular invasion, bowel obstruction, < 12 lymph nodes examined, perineural invasion, localized perforation, or close, indeterminate or positive margins. As for the adding oxaliplatin, according to the subgroup analysis of MOSAIC and NSABP C-07 trial, no significant benefit was found by adding oxaliplatin to 5-FU and leucovorin to stage II colon cancer [5,6]. Therefore, considering the potential risk of side effects of oxaliplatin including neuropathy, it is not recommended to adding oxaliplatin in stage II colon cancer patients. Another factors should be considered is mismatch repair or MSI testing. it should be performed before deciding adjuvant chemotherapy for stage II colon cancer, because MSI-H patients may have a good prognosis and do not benefit from 5-FU adjuvant therapy [7]. The authors tried to find which patient could omit the adjuvant chemotherapy in stage II colon cancer. And they found that the patients with only one high-risk factor for the recurrence may not have significant benefit by adjuvant chemotherapy [8]. However, it should be interpreted cautiously, because to prove a small potential benefit of adjuvant chemotherapy in stage II colon cancer, large population are inevitably needed. In conclusion, considering all above factors, conversation between clinicians and patients regarding the potential risks and benefits with adjuvant chemotherapy for stage II colon cancers is very important for decision making. And personalized treatment should be performed. Editorial Korean Journal of Clinical Oncology 2018;14:67-68 https://doi.org/10.14216/kjco.18012 pISSN 1738-8082 ∙ eISSN 2288-4084
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