Department of Dermatology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology (HUST), Wuhan, China.
Hubei Engineering Research Center for Skin Repair and Theranostics, Wuhan, China.
Cancer Med. 2020 Jul;9(13):4561-4571. doi: 10.1002/cam4.3065. Epub 2020 May 5.
This study aimed to assess the independent prognostic value of tumor size compared with other clinical and pathologic features of primary invasive cutaneous melanoma (CM).
This study included 28,593 patients with primary invasive CM in Surveillance, Epidemiology, and End Results Program database diagnosed from 2004 through 2016. Tumor size was divided into five subgroups (≤6, 7-12, 13-30, 31-42, and >42 mm). The primary endpoint was melanoma-specific survival (MSS).
The relationship between tumor size and survival was piecewise. After adjusting for age, sex, primary site, histopathologic cell type, Breslow thickness, ulceration, mitotic rate, regional metastasis, and distant metastasis, the hazard ratio (HR) of MSS increased with increasing tumor size until a peak at 31-42 mm (HRs, 1.33, 1.59, 2.41, respectively; all P < .0001), and then decreased when tumor size was larger than 42 mm using tumor size ≤ 6 mm as the reference (HR, 2.11; 95% confidence interval [CI], 1.84 -2.42; P < .0001). This pattern mostly remained after stratification by T subcategories from T1 to T4 in localized primary CM except that tumor size >42 mm subgroup had the shortest MSS in T4. In addition, tumor size with a cutoff value of 12 mm showed stronger prognostic value for MSS (HR, 2.32; 95% CI, 1.80-2.98; P < .0001) than Breslow thickness and mitotic rate in primary CM with T1N0M0.
Tumor size was an important independent prognostic factor for MSS in patients with primary invasive CM. Tumor size larger than 30 mm would provide additional and important prognostic information in each T subcategory of localized CM. Furthermore, tumor size with a cutoff value of 12 mm has great potential in improving the accuracy of melanoma T1 substaging.
本研究旨在评估肿瘤大小与原发性侵袭性皮肤黑色素瘤(CM)的其他临床和病理特征相比的独立预后价值。
本研究纳入了 2004 年至 2016 年间监测、流行病学和结果计划(SEER)数据库中诊断的 28593 例原发性侵袭性 CM 患者。肿瘤大小分为五组(≤6、7-12、13-30、31-42 和 >42mm)。主要终点为黑色素瘤特异性生存(MSS)。
肿瘤大小与生存之间存在分段关系。调整年龄、性别、原发部位、组织病理学细胞类型、Breslow 厚度、溃疡、有丝分裂率、区域转移和远处转移后,MSS 的风险比(HR)随肿瘤大小的增加而增加,直至 31-42mm 时达到峰值(HR 分别为 1.33、1.59、2.41;均 P<.0001),然后当肿瘤大小大于 42mm 时(以肿瘤大小≤6mm 为参考)下降(HR 为 2.11;95%置信区间 [CI],1.84-2.42;P<.0001)。除 T4 期肿瘤大小>42mm 亚组 MSS 最短外,局部原发性 CM 的 T1 至 T4 亚分类分层后,这种模式基本保持不变。此外,肿瘤大小的截断值为 12mm 时,在 T1N0M0 期原发性 CM 中对 MSS 的预后价值强于 Breslow 厚度和有丝分裂率(HR 为 2.32;95%CI,1.80-2.98;P<.0001)。
肿瘤大小是原发性侵袭性 CM 患者 MSS 的重要独立预后因素。肿瘤大小大于 30mm 可在每个局部 CM 的 T 亚分类中提供额外的重要预后信息。此外,肿瘤大小的截断值为 12mm 在提高黑色素瘤 T1 亚分期的准确性方面具有很大潜力。