Barts Cancer Institute, Barts Experimental Cancer Medicine Centre, Bart and the London NHS Trust, London, United Kingdom.
Clin Genitourin Cancer. 2012 Dec;10(4):213-8. doi: 10.1016/j.clgc.2012.06.002. Epub 2012 Aug 30.
Targeted therapy has changed the treatment of metastatic renal cell carcinoma (mRCC). However, it is unclear if patients need to start systemic therapy immediately or if treatment can be deferred. Identification of the appropriate time to discontinue therapy is also uncertain. We reviewed treatment guidelines and trials evaluating targeted agents for mRCC to assess the evidence regarding commencing and discontinuing therapy for mRCC. Guidelines recommend that patients with mRCC receive targeted agents; however, they do not address when therapy should start. Risk factors based on Memorial Sloan-Kettering Cancer Center (MSKCC) or Heng criteria can be used to stratify patients. MSKCC prognostic factors include Karnofsky performance status (< 80%), high lactate dehydrogenase levels, low hemoglobin levels, high serum calcium levels, and time from diagnosis to start of therapy < 1 year. In patients with poor and intermediate risk (≥ 3 and 1-2 factors, respectively) and/or with high tumor burden, targeted therapy should commence as soon as possible. In patients with MSKCC good-risk disease and few disease symptoms, active surveillance may be appropriate. Regular monitoring is required so that treatment can be initiated upon evidence of active disease. Second-line therapy is usually commenced after disease progression; however, because of the limitations of radiologic assessment of response to targeted therapies, other factors may need to be considered to guide decisions regarding stopping or switching therapy. These include scenarios such as a mixed response to therapy. For selected patients at favorable risk, active surveillance may be feasible; however, strict monitoring is required.
靶向治疗改变了转移性肾细胞癌(mRCC)的治疗方法。然而,目前尚不清楚患者是否需要立即开始全身治疗,或者是否可以推迟治疗。何时停止治疗也不确定。我们回顾了评估 mRCC 靶向药物的治疗指南和试验,以评估关于开始和停止 mRCC 治疗的证据。指南建议 mRCC 患者接受靶向药物治疗;但是,它们没有说明何时开始治疗。可以使用基于 Memorial Sloan-Kettering Cancer Center(MSKCC)或 Heng 标准的风险因素对患者进行分层。MSKCC 预后因素包括 Karnofsky 表现状态(<80%)、乳酸脱氢酶水平高、血红蛋白水平低、血清钙水平高以及从诊断到开始治疗的时间<1 年。对于风险较高和中等的患者(分别为≥3 个和 1-2 个因素)和/或肿瘤负荷较高的患者,应尽快开始靶向治疗。对于 MSKCC 预后良好且疾病症状较少的患者,主动监测可能是合适的。需要定期监测,以便在出现疾病活动的证据时开始治疗。二线治疗通常在疾病进展后开始;但是,由于对靶向治疗反应的影像学评估存在局限性,可能需要考虑其他因素来指导停止或转换治疗的决策。这些因素包括治疗反应混合等情况。对于风险较低的选定患者,主动监测可能是可行的;但是,需要严格监测。