Peninsula Dermatology, Burlingame, California.
Department of Dermatology, Universitario de Salamanca, Salamanca, Spain.
Int J Radiat Oncol Biol Phys. 2024 Nov 1;120(3):760-771. doi: 10.1016/j.ijrobp.2024.05.022. Epub 2024 May 27.
Adjuvant radiation therapy (ART) for cutaneous squamous cell carcinoma is recommended based on a number of wide-ranging clinicopathologic features, which encompass a broad array of patients. The 40-gene expression profile (GEP) test classifies cutaneous squamous cell carcinoma tumors into low (class 1), higher (class 2A), or highest (class 2B) risk of nodal and/or distant metastasis. This study's hypotheses are as follows: (1) local recurrence is associated with metastatic disease progression and (2) 40-GEP, by identifying high risk for metastasis, could predict a metastasis-specific benefit from ART.
Samples were obtained from 920 patients (ART-untreated: 496 class 1, 335 class 2A, and 33 class 2B; ART-treated: 11 class 1, 35 class 2A, and 10 class 2B) who were matched on clinical risk factors and stratified by ART status to create 49 matched patient strata. To control for the variety of characteristics and treatment selection bias, randomly sampled pairs of matched ART and non-ART patients comprising 10,000 resampled cohorts were each analyzed for 5-year metastasis-free survival and predicted time to metastatic event.
Of 96 patients experiencing local recurrence, 56.3% experienced metastasis; of those experiencing both, 88.9% experienced local recurrence before (75.9%) or concurrently (13.0%) with metastasis. After matching for clinicopathologic risk, median 5-year disease progression rates for resampled cohorts demonstrated approximately 50% improvement for class 2B ART-treated compared with ART-untreated cohorts. ART-treated class 2B cohorts had a 5-fold delay in predicted time to metastatic event and deceleration of disease progression compared with ART-untreated cohorts (Kolmogorov-Smirnov test, P < .01); this was not observed for patients with class 1 or 2A cSCC (P > .05 for each). No risk factor or staging system combined with ART status identified groups that would benefit from ART as well as 40-GEP.
Forty-GEP identifies patients at the highest risk of nodal/distant metastasis who may derive the greatest benefit from ART, as well as patients who may have clinical indications for ART but are at low risk of metastasis. Compared with current guidelines, 40-GEP could provide greater specificity concerning the benefit of ART in individual patients.
根据广泛的临床病理特征,建议对皮肤鳞状细胞癌进行辅助放射治疗(ART),这些特征涵盖了广泛的患者群体。40 基因表达谱(GEP)测试将皮肤鳞状细胞癌肿瘤分为低(1 类)、较高(2A 类)或最高(2B 类)淋巴结和/或远处转移风险。本研究的假设如下:(1)局部复发与转移疾病进展相关,(2)40-GEP 通过识别转移高风险,可预测 ART 对转移的特异性获益。
对 920 名患者(未经 ART 治疗:496 例 1 类,335 例 2A 类,33 例 2B 类;经 ART 治疗:11 例 1 类,35 例 2A 类,10 例 2B 类)的样本进行了检测,这些患者根据临床危险因素进行了匹配,并按 ART 状态进行了分层,以创建 49 个匹配患者层。为了控制各种特征和治疗选择偏差,对包含 10,000 个抽样队列的每个 ART 和非 ART 患者的随机抽样对进行了 5 年无转移生存率和预测转移事件时间的分析。
在 96 名发生局部复发的患者中,56.3%发生了转移;在同时发生局部复发和转移的患者中,88.9%在转移之前(75.9%)或同时(13.0%)发生了局部复发。在匹配临床病理风险后,抽样队列的中位 5 年疾病进展率表明,与未经 ART 治疗的队列相比,2B 类 ART 治疗的队列的改善约为 50%。与未经 ART 治疗的队列相比,ART 治疗的 2B 类队列的预测转移事件时间延迟了 5 倍,疾病进展速度也有所减缓(柯尔莫哥洛夫-斯米尔诺夫检验,P<.01);而 1 类或 2A 类 cSCC 患者则无此现象(每种情况下 P>.05)。没有任何风险因素或分期系统与 ART 状态相结合,可以识别出受益于 ART 的人群,以及可能有 ART 临床适应证但转移风险较低的人群。与现有指南相比,40-GEP 可以为个体患者接受 ART 的获益提供更高的特异性。