Dell Medical School, The University of Texas at Austin, Austin.
Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill.
JAMA Dermatol. 2023 Jul 1;159(7):703-710. doi: 10.1001/jamadermatol.2023.1494.
The incidence of melanoma in situ (MIS) is increasing more rapidly than any invasive or in situ cancer in the US. Although more than half of melanomas diagnosed are MIS, information about long-term prognosis following a diagnosis of MIS remains unknown.
To evaluate mortality and factors associated with mortality after a diagnosis of MIS.
DESIGN, SETTING, AND PARTICIPANTS: This population-based cohort study of adults with a diagnosis of first primary MIS from 2000 to 2018 included data from the US Surveillance, Epidemiology, and End Results Program, which were analyzed from July to September 2022.
Mortality after a diagnosis of MIS was evaluated using 15-year melanoma-specific survival, 15-year relative survival (ie, compared with similar individuals without MIS), and standardized mortality ratios (SMRs). Cox regression was used to estimate hazard ratios (HRs) for death by demographic and clinical characteristics.
Among 137 872 patients with a first-and-only MIS, the mean (SD) age at diagnosis was 61.9 (16.5) years (64 027 women [46.4%]; 239 [0.2%] American Indian or Alaska Native, 606 [0.4%] Asian, 344 [0.2%] Black, 3348 [2.4%] Hispanic, and 133 335 [96.7%] White individuals). Mean (range) follow-up was 6.6 (0-18.9) years. The 15-year melanoma-specific survival was 98.4% (95% CI, 98.3%-98.5%), whereas the 15-year relative survival was 112.4% (95% CI, 112.0%-112.8%). The melanoma-specific SMR was 1.89 (95% CI, 1.77-2.02); however, the all-cause SMR was 0.68 (95% CI, 0.67-0.7). Risk of melanoma-specific mortality was higher for older patients (7.4% for those 80 years or older vs 1.4% for those aged 60-69 years; adjusted HR, 8.2; 95% CI, 6.7-10.0) and patients with acral lentiginous histology results (3.3% for acral lentiginous vs 0.9% for superficial spreading; HR, 5.3; 95% CI, 2.3-12.3). Of patients with primary MIS, 6751 (4.3%) experienced a second primary invasive melanoma and 11 628 (7.4%) experienced a second primary MIS. Compared with patients without a subsequent melanoma, the risk of melanoma-specific mortality was increased for those with a second primary invasive melanoma (adjusted HR, 4.1; 95% CI, 3.6-4.6) and was decreased for those with a second primary MIS (adjusted HR, 0.7; 95% CI, 0.6-0.9).
The results of this cohort study suggest that patients with a diagnosis of MIS have an increased but low risk of melanoma-specific mortality and live longer than people in the general population, suggesting that there is significant detection of low-risk disease among health-seeking individuals. Factors associated with death following MIS include older age (≥80 years) and subsequent primary invasive melanoma.
在美国,原位黑色素瘤(MIS)的发病率增长速度比任何侵袭性或原位癌症都要快。尽管超过一半的黑色素瘤被诊断为 MIS,但关于 MIS 诊断后长期预后的信息仍不清楚。
评估 MIS 诊断后死亡率和与死亡率相关的因素。
设计、地点和参与者:这项基于人群的队列研究纳入了 2000 年至 2018 年期间首次被诊断为原发性 MIS 的成年人的数据,这些数据来自美国监测、流行病学和最终结果计划,研究分析于 2022 年 7 月至 9 月进行。
通过 15 年黑色素瘤特异性生存率、15 年相对生存率(即与无 MIS 的相似个体相比)和标准化死亡率比(SMR)来评估 MIS 诊断后的死亡率。使用 Cox 回归估计按人口统计学和临床特征的死亡风险比(HR)。
在 137872 名首次且唯一 MIS 的患者中,诊断时的平均(SD)年龄为 61.9(16.5)岁(64027 名女性[46.4%];239 名[0.2%]美国印第安人或阿拉斯加原住民,606 名[0.4%]亚洲人,344 名[0.2%]黑人,3348 名[2.4%]西班牙裔,133335 名[96.7%]白人)。平均(范围)随访时间为 6.6(0-18.9)年。15 年黑色素瘤特异性生存率为 98.4%(95%CI,98.3%-98.5%),而 15 年相对生存率为 112.4%(95%CI,112.0%-112.8%)。黑色素瘤特异性 SMR 为 1.89(95%CI,1.77-2.02);然而,全因 SMR 为 0.68(95%CI,0.67-0.7)。黑色素瘤特异性死亡率风险较高的患者为年龄较大的患者(80 岁及以上者为 7.4%,60-69 岁者为 1.4%;调整后的 HR,8.2;95%CI,6.7-10.0)和肢端雀斑样黑色素瘤组织学结果的患者(肢端雀斑样黑色素瘤为 3.3%,浅表扩散性黑色素瘤为 0.9%;HR,5.3;95%CI,2.3-12.3)。在原发性 MIS 的患者中,有 6751 名(4.3%)患者发生了第二原发性侵袭性黑色素瘤,11628 名(7.4%)患者发生了第二原发性 MIS。与没有后续黑色素瘤的患者相比,有第二原发性侵袭性黑色素瘤的患者黑色素瘤特异性死亡率风险增加(调整后的 HR,4.1;95%CI,3.6-4.6),而有第二原发性 MIS 的患者黑色素瘤特异性死亡率风险降低(调整后的 HR,0.7;95%CI,0.6-0.9)。
这项队列研究的结果表明,MIS 诊断后的患者黑色素瘤特异性死亡率虽然增加但风险较低,且比一般人群寿命更长,这表明在寻求医疗的人群中存在大量低风险疾病的检测。与 MIS 相关的死亡因素包括年龄较大(≥80 岁)和随后的侵袭性黑色素瘤。