Relationships between survival and real-world recurrence-free survival or distant metastasis-free survival among patients with completely resected stage IIB or IIC melanoma.

IF 1.5 4区 医学 Q3 DERMATOLOGY Melanoma Research Pub Date : 2024-08-01 Epub Date: 2024-05-27 DOI:10.1097/CMR.0000000000000962
Wolfram Samlowski, Michelle A Silver, Andriana Hohlbauch, Shujing Zhang, Mizuho Fukunaga-Kalabis, Clemens Krepler, Yunfei Wang, Ila Sruti, Ruixuan Jiang
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Abstract

Long follow-up time is needed for overall survival (OS) data to mature for early-stage melanoma. This retrospective study aimed to describe the relationships between OS and two intermediate endpoints - real-world recurrence-free survival (rwRFS) and real-world distant metastasis-free survival (rwDMFS) - for patients with stage IIB or IIC melanoma that was completely resected from 1 January 2008 to 31 December 2017, with follow-up to 31 December 2020. We used three different approaches to describe the relationships: estimates of correlation using Kendall τ rank correlation; comparisons of all-cause survival with/without recurrence or distant metastasis using adjusted Cox proportional hazard models; and landmark analyses of all-cause survival stratified by recurrence status at 1-5 years. During a 39-month median follow-up from surgical resection, 223/567 patients (39%) experienced recurrence, among whom 171/567 patients (30%) developed distant metastasis. Median OS from surgical resection was 117.6 months [95% confidence interval (CI), 104.7-not reached], median rwRFS was 49.8 months (95% CI, 39.6-61.0), and median rwDMFS was 70.9 months (95% CI, 58.4-89.1). We observed strong correlations between rwRFS and OS, and between rwDMFS and OS (Kendall τ of 0.73 and 0.82, respectively). Risk of death was significantly greater after recurrence (all-cause survival adjusted hazard ratio [HR], 7.48; 95% CI, 4.55-12.29) or distant metastasis (adjusted HR, 11.00; 95% CI, 6.92-17.49). Risk of death remained significantly elevated with recurrence or distant metastasis by landmark years 1, 3, and 5 after surgical resection. These findings support the use of recurrence/rwRFS and distant metastasis/rwDMFS as surrogate endpoints for OS after complete resection of stage IIB or IIC melanoma.

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完全切除的 IIB 期或 IIC 期黑色素瘤患者的生存期与实际无复发生存期或无远处转移生存期之间的关系。
早期黑色素瘤的总生存期(OS)数据需要长时间的随访才能成熟。这项回顾性研究旨在描述2008年1月1日至2017年12月31日期间完全切除的IIB或IIC期黑色素瘤患者的OS与两个中间终点--实际无复发生存期(rwRFS)和实际无远处转移生存期(rwDMFS)--之间的关系,随访至2020年12月31日。我们使用了三种不同的方法来描述这些关系:使用 Kendall τ 秩相关性估计相关性;使用调整后的 Cox 比例危险模型比较有/无复发或远处转移的全因生存率;以及根据 1-5 年的复发状况对全因生存率进行分层的地标分析。在手术切除后39个月的中位随访期间,223/567例患者(39%)出现复发,其中171/567例患者(30%)出现远处转移。手术切除后的中位 OS 为 117.6 个月[95% 置信区间 (CI),104.7-未达到],中位 rwRFS 为 49.8 个月 (95% CI,39.6-61.0),中位 rwDMFS 为 70.9 个月 (95% CI,58.4-89.1)。我们观察到rwRFS和OS之间以及rwDMFS和OS之间存在很强的相关性(Kendall τ分别为0.73和0.82)。复发(全因生存调整后危险比[HR],7.48;95% CI,4.55-12.29)或远处转移(调整后危险比,11.00;95% CI,6.92-17.49)后死亡风险明显增加。在手术切除后的第1、3和5年,复发或远处转移的死亡风险仍明显升高。这些研究结果支持将复发/rwRFS和远处转移/rwDMFS作为IIB期或IIC期黑色素瘤完全切除术后OS的替代终点。
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来源期刊
Melanoma Research
Melanoma Research 医学-皮肤病学
CiteScore
3.40
自引率
4.50%
发文量
139
审稿时长
6-12 weeks
期刊介绍: ​​​​​​Melanoma Research is a well established international forum for the dissemination of new findings relating to melanoma. The aim of the Journal is to promote the level of informational exchange between those engaged in the field. Melanoma Research aims to encourage an informed and balanced view of experimental and clinical research and extend and stimulate communication and exchange of knowledge between investigators with differing areas of expertise. This will foster the development of translational research. The reporting of new clinical results and the effect and toxicity of new therapeutic agents and immunotherapy will be given emphasis by rapid publication of Short Communications. ​Thus, Melanoma Research seeks to present a coherent and up-to-date account of all aspects of investigations pertinent to melanoma. Consequently the scope of the Journal is broad, embracing the entire range of studies from fundamental and applied research in such subject areas as genetics, molecular biology, biochemistry, cell biology, photobiology, pathology, immunology, and advances in clinical oncology influencing the prevention, diagnosis and treatment of melanoma.
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