Norfolk and Norwich University Hospital NHS Trust, Norwich, United Kingdom.
Melanoma Institute of Australia, The University of Sydney, Sydney, New South Wales, Australia.
J Clin Oncol. 2022 Dec 1;40(34):3940-3951. doi: 10.1200/JCO.21.02488. Epub 2022 Jul 18.
Indications for offering adjuvant systemic therapy for patients with early-stage melanomas with low disease burden sentinel node (SN) micrometastases, namely, American Joint Committee on Cancer (AJCC; eighth edition) stage IIIA disease, are presently controversial. The current study sought to identify high-risk SN-positive AJCC stage IIIA patients who are more likely to derive benefit from adjuvant systemic therapy.
Patients were recruited from an intercontinental (Australia/Europe/North America) consortium of nine high-volume cancer centers. All were adult patients with pathologic stage pT1b/pT2a primary cutaneous melanomas who underwent SN biopsy between 2005 and 2020. Patient data, primary tumor and SN characteristics, and survival outcomes were analyzed.
Three thousand six hundred seven patients were included. The median follow-up was 34 months. Pairwise disease comparison demonstrated no significant survival difference between N1a and N2a subgroups. Survival analysis identified a SN tumor deposit maximum dimension of 0.3 mm as the optimal cut point for stratifying survival. Five-year disease-specific survival rates were 80.3% and 94.1% for patients with SN metastatic tumor deposits ≥ 0.3 mm and < 0.3 mm, respectively (hazard ratio, 1.26 [1.11 to 1.44]; < .0001). Similar findings were seen for overall disease-free and distant metastasis-free survival. There were no survival differences between the AJCC IB patients and low-risk (< 0.3 mm) AJCC IIIA patients. The newly identified high-risk (≥ 0.3 mm) subgroup comprised 271 (66.4%) of the AJCC IIIA cohort, whereas only 142 (34.8%) patients had SN tumor deposits > 1 mm in maximum dimension.
Patients with AJCC IIIA melanoma with SN tumor deposits ≥ 0.3 mm in maximum dimension are at higher risk of disease progression and may benefit from adjuvant systemic therapy or enrollment into a clinical trial. Patients with SN deposits < 0.3 mm in maximum dimension can be managed similar to their SN-negative, AJCC IB counterparts, thereby avoiding regular radiological surveillance and more intensive follow-up.
对于低疾病负担前哨淋巴结(SN)微转移的早期黑色素瘤患者,即美国癌症联合委员会(AJCC;第八版)分期 IIIA 期患者,提供辅助全身治疗的适应证目前存在争议。本研究旨在确定更有可能从辅助全身治疗中获益的高危 SN 阳性 AJCC IIIA 期患者。
本研究从一个由 9 个大容量癌症中心组成的洲际(澳大利亚/欧洲/北美)联盟中招募患者。所有患者均为接受 SN 活检的 2005 年至 2020 年间病理分期为 pT1b/pT2a 原发性皮肤黑色素瘤的成年患者。分析了患者数据、原发肿瘤和 SN 特征以及生存结局。
共纳入 3670 例患者。中位随访时间为 34 个月。疾病两两比较显示 N1a 和 N2a 亚组之间的生存无显著差异。生存分析确定 SN 肿瘤转移灶最大直径 0.3mm 为分层生存的最佳切点。SN 转移性肿瘤沉积≥0.3mm 和<0.3mm 的患者 5 年疾病特异性生存率分别为 80.3%和 94.1%(危险比,1.26[1.11 至 1.44];<0.0001)。总无病生存率和远处无转移生存率也有类似发现。AJCC IB 患者与低危(<0.3mm)AJCC IIIA 患者的生存无差异。新确定的高危(≥0.3mm)亚组包括 AJCC IIIA 队列中的 271(66.4%)例患者,而仅有 142(34.8%)例患者的 SN 肿瘤沉积最大直径>1mm。
SN 肿瘤沉积最大直径≥0.3mm 的 AJCC IIIA 黑色素瘤患者疾病进展风险较高,可能受益于辅助全身治疗或入组临床试验。SN 沉积最大直径<0.3mm 的患者可以与 SN 阴性、AJCC IB 对应的患者类似管理,从而避免常规影像学监测和更密集的随访。