John Wayne Cancer Institute at Saint John's Health Center, 2200 Santa Monica Blvd, Santa Monica, CA 90404, USA.
J Clin Oncol. 2012 Nov 1;30(31):3819-26. doi: 10.1200/JCO.2011.40.0887. Epub 2012 Sep 24.
The outcomes of patients with melanoma who have sentinel lymph node (SLN) metastases can be highly variable, which has precluded establishment of consensus regarding treatment of the group. The detection of high-risk patients from this clinical setting may be helpful for determination of both prognosis and management. We report the utility of multimarker reverse-transcriptase quantitative polymerase chain reaction (RT-qPCR) detection of circulating tumor cells (CTCs) in patients with melanoma diagnosed with SLN metastases in a phase III, international, multicenter clinical trial.
Blood specimens were collected from patients with melanoma (n = 331) who were clinically disease-free after complete lymphadenectomy (CLND) before entering onto a randomized adjuvant melanoma vaccine plus bacillus Calmette-Guérin (BCG) versus BCG placebo trial from 30 melanoma centers (United States and international). Blood was assessed using a verified multimarker RT-qPCR assay (MART-1, MAGE-A3, and GalNAc-T) of melanoma-associated proteins. Cox regression analyses were used to evaluate the prognostic significance of CTC status for disease recurrence and melanoma-specific survival (MSS).
Individual CTC biomarker detection ranged from 13.4% to 17.5%. There was no association of CTC status (zero to one positive biomarkers v two or more positive biomarkers) with known clinical or pathologic prognostic variables. However, two or more positive biomarkers was significantly associated with worse distant metastasis disease-free survival (hazard ratio [HR] = 2.13, P = .009) and reduced recurrence-free survival (HR = 1.70, P = .046) and MSS (HR = 1.88, P = .043) in a multivariable analysis.
CTC biomarker status is a prognostic factor for recurrence-free survival, distant metastasis disease-free survival, and MSS after CLND in patients with SLN metastasis. This multimarker RT-qPCR analysis may therefore be useful in discriminating patients who may benefit from aggressive adjuvant therapy or stratifying patients for adjuvant clinical trials.
患有前哨淋巴结(SLN)转移的黑色素瘤患者的预后结果可能存在高度变异性,这使得针对该人群的治疗方法无法达成共识。从这一临床背景中检测出高危患者,可能有助于确定预后和管理。我们报告了在一项 III 期、国际、多中心临床试验中,使用多标志物逆转录定量聚合酶链反应(RT-qPCR)检测黑色素瘤患者 SLN 转移后循环肿瘤细胞(CTC)的效用。
在完全淋巴结清扫术(CLND)后临床无疾病的黑色素瘤患者(n = 331)入组一项随机辅助黑色素瘤疫苗加卡介苗(BCG)与 BCG 安慰剂试验前,从 30 个黑色素瘤中心采集血液标本(美国和国际)。使用已验证的多标志物 RT-qPCR 检测黑色素瘤相关蛋白(MART-1、MAGE-A3 和 GalNAc-T)评估血液。Cox 回归分析用于评估 CTC 状态对疾病复发和黑色素瘤特异性生存(MSS)的预后意义。
单独的 CTC 生物标志物检测范围为 13.4%至 17.5%。CTC 状态(零到一个阳性生物标志物与两个或更多阳性生物标志物)与已知的临床或病理预后变量无关。然而,两个或更多阳性标志物与远处转移无病生存率(危险比 [HR] = 2.13,P =.009)和无复发生存率(HR = 1.70,P =.046)以及 MSS(HR = 1.88,P =.043)显著相关。多变量分析。
在 SLN 转移的黑色素瘤患者 CLND 后,CTC 生物标志物状态是无复发生存率、远处转移无病生存率和 MSS 的预后因素。这种多标志物 RT-qPCR 分析可能有助于区分可能受益于强化辅助治疗的患者或分层患者进行辅助临床试验。