Handel Eleanor E, McKeown Janet, Wei Joe, Kankaria Roma A, Burnette Hannah, Johnson Douglas B, Lawless Aleigha, Czapla Juliane, Sullivan Ryan J, Albrecht Lea Jessica, Zimmer Lisa, Mangana Joanna, Dummer Reinhard, Kessels Jolien I, Neyns Bart, Allayous Clara, Lebbe Celeste, Boatwright Christina, Mehnert Janice M, Ottaviano Margaret, Ascierto Paolo A, Czarnecka Anna M, Rutkowski Piotr, Lo Serigne N, Long Georgina V, Menzies Alexander M, Carlino Matteo S
Crown Princess Mary Cancer Centre, Westmead Hospital, Sydney, NSW, Australia.
Melanoma Institute Australia, The University of Sydney, Sydney, NSW, Australia.
Eur J Cancer. 2025 Jan 17;215:115171. doi: 10.1016/j.ejca.2024.115171. Epub 2024 Dec 9.
Immune checkpoint inhibitors (ICI) can achieve durable responses in patients with advanced melanoma, and results from clinical trials suggest cure may be possible for a subset of patients. Despite clinical trial data, little is known about the risk, character, and clinical outcome of late recurrences after ICI. This study aimed to explore the disease outcomes and survival in a cohort of patients with long-term responses to ICI. We retrospectively identified patients treated with ICI for advanced melanoma with long-term disease control, defined as not requiring a subsequent line of systemic therapy within 3 years of ICI commencement. We analysed disease characteristics, treatment, toxicity, recurrence patterns, management, and outcomes. A total of 567 patients were identified with a median follow-up of 7.1 years: 504 (89 %) without disease progression within 3 years (cohort 1) and 63 (11.1 %) with disease progression within 3 years managed without a change in systemic therapy (cohort 2). Subsequent progression after 3 years occurred for 39 (7.7 %) patients in cohort 1, compared to 14 (22 %) in cohort 2. Predictors for late progression after 3 years were a non-complete radiological response (CR) best response and prior progression within 3 years. Thirty-two patients (5.6 %) died during follow-up, 8 (1.4 %) from melanoma, 6 (1.2 %) from cohort 1 and 2 (3.2 %) from cohort 2. In this population of patients with advanced melanoma with long-term disease control from ICI, the risk of subsequent disease progression and death was low. This suggests that a significant proportion of long-term ICI responders are likely cured and may inform the frequency and duration of follow-up.
免疫检查点抑制剂(ICI)可使晚期黑色素瘤患者获得持久缓解,临床试验结果表明部分患者可能治愈。尽管有临床试验数据,但对于ICI治疗后晚期复发的风险、特征及临床结局仍知之甚少。本研究旨在探讨一组对ICI有长期反应的患者的疾病转归及生存情况。我们回顾性确定了接受ICI治疗的晚期黑色素瘤患者,这些患者具有长期疾病控制,定义为在ICI开始后3年内无需后续全身治疗。我们分析了疾病特征、治疗、毒性、复发模式、处理及结局。共确定了567例患者,中位随访时间为7.1年:504例(89%)在3年内无疾病进展(队列1),63例(11.1%)在3年内有疾病进展但未改变全身治疗(队列2)。队列1中39例(7.7%)患者在3年后出现后续进展,而队列2中为14例(22%)。3年后晚期进展的预测因素为非完全放射学缓解(CR)最佳反应及3年内既往进展。32例患者(5.6%)在随访期间死亡,8例(1.4%)死于黑色素瘤,队列1中有6例(1.2%),队列2中有2例(3.2%)。在这组接受ICI获得长期疾病控制的晚期黑色素瘤患者中,后续疾病进展和死亡风险较低。这表明相当一部分长期ICI反应者可能已治愈,并可为随访频率和持续时间提供参考。