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晚期黑色素瘤中伊匹单抗和非伊匹单抗治疗的长期真实世界经验:IMAGE 研究。

Long-term real-world experience with ipilimumab and non-ipilimumab therapies in advanced melanoma: the IMAGE study.

机构信息

Hospices Civils de Lyon, Centre Hospitalier Lyon-Sud, 69495, Pierre-Bénite, France.

Université de Lille, INSERM U1189, CHRU Lille, 59037, Lille, France.

出版信息

BMC Cancer. 2021 May 29;21(1):642. doi: 10.1186/s12885-021-08032-y.

Abstract

BACKGROUND

Ipilimumab has shown long-term overall survival (OS) in patients with advanced melanoma in clinical trials, but robust real-world evidence is lacking. We present long-term outcomes from the IMAGE study (NCT01511913) in patients receiving ipilimumab and/or non-ipilimumab (any approved treatment other than ipilimumab) systemic therapies.

METHODS

IMAGE was a multinational, prospective, observational study assessing adult patients with advanced melanoma treated with ipilimumab or non-ipilimumab systemic therapies between June 2012 and March 2015 with ≥3 years of follow-up. Adjusted OS curves based on multivariate Cox regression models included covariate effects. Safety and patient-reported outcomes were assessed.

RESULTS

Among 1356 patients, 1094 (81%) received ipilimumab and 262 (19%) received non-ipilimumab index therapy (systemic therapy [chemotherapy, anti-programmed death 1 antibodies, or BRAF ± MEK inhibitors], radiotherapy, and radiosurgery). In the overall population, median age was 64 years, 60% were male, 78% were from Europe, and 78% had received previous treatment for advanced melanoma. In the ipilimumab-treated cohort, 780 (71%) patients did not receive subsequent therapy (IPI-noOther) and 314 (29%) received subsequent non-ipilimumab therapy (IPI-Other) on study. In the non-ipilimumab-treated cohort, 205 (78%) patients remained on or received other subsequent non-ipilimumab therapy (Other-Other) and 57 (22%) received subsequent ipilimumab therapy (Other-IPI) on study. Among 1151 patients who received ipilimumab at any time during the study (IPI-noOther, IPI-Other, and Other-IPI), 296 (26%) reported CTCAE grade ≥ 3 treatment-related adverse events, most occurring in year 1. Ipilimumab-treated and non-ipilimumab-treated patients who switched therapy (IPI-Other and Other-IPI) had longer OS than those who did not switch (IPI-noOther and Other-Other). Patients with prior therapy who did not switch therapy (IPI-noOther and Other-Other) showed similar OS. In treatment-naive patients, those in the IPI-noOther group tended to have longer OS than those in the Other-Other group. Patient-reported outcomes were similar between treatment cohorts.

CONCLUSIONS

With long-term follow-up (≥ 3 years), safety and OS in this real-world population of patients treated with ipilimumab 3 mg/kg were consistent with those reported in clinical trials. Patient-reported quality of life was maintained over the study period. OS analysis across both pretreated and treatment-naive patients suggested a beneficial role of ipilimumab early in treatment.

TRIAL REGISTRATION

ClinicalTrials.gov , NCT01511913. Registered January 19, 2012 - Retrospectively registered, https://clinicaltrials.gov/ct2/show/NCT01511913.

摘要

背景

依匹单抗在临床试验中显示出晚期黑色素瘤患者的长期总生存期(OS),但缺乏强有力的真实世界证据。我们展示了 IMAGE 研究(NCT01511913)中接受依匹单抗和/或非依匹单抗(除依匹单抗以外的任何批准治疗)全身治疗的患者的长期结果。

方法

IMAGE 是一项多中心、前瞻性、观察性研究,评估了 2012 年 6 月至 2015 年 3 月期间接受依匹单抗或非依匹单抗全身治疗的晚期黑色素瘤成年患者,随访时间≥3 年。基于多变量 Cox 回归模型的调整 OS 曲线包括协变量的影响。评估了安全性和患者报告的结果。

结果

在 1356 例患者中,1094 例(81%)接受了依匹单抗治疗,262 例(19%)接受了非依匹单抗指数治疗(全身治疗[化疗、抗程序性死亡 1 抗体或 BRAF ± MEK 抑制剂]、放疗和放射外科)。在总体人群中,中位年龄为 64 岁,60%为男性,78%来自欧洲,78%接受过晚期黑色素瘤的既往治疗。在依匹单抗治疗组中,780 例(71%)患者未接受后续治疗(IPI-noOther),314 例(29%)在研究期间接受了后续非依匹单抗治疗(IPI-Other)。在非依匹单抗治疗组中,205 例(78%)患者继续接受或接受了其他后续非依匹单抗治疗(Other-Other),57 例(22%)在研究期间接受了后续依匹单抗治疗(Other-IPI)。在研究期间任何时候接受过依匹单抗治疗的 1151 例患者(IPI-noOther、IPI-Other 和 Other-IPI)中,296 例(26%)报告了 CTCAE 分级≥3 的治疗相关不良事件,大多数发生在第 1 年。接受依匹单抗和非依匹单抗治疗且接受了治疗转换的患者(IPI-Other 和 Other-IPI)的 OS 长于未接受治疗转换的患者(IPI-noOther 和 Other-Other)。未接受治疗转换的有既往治疗史的患者(IPI-noOther 和 Other-Other)的 OS 相似。在初治患者中,IPI-noOther 组的患者倾向于比 Other-Other 组的患者有更长的 OS。治疗组之间的患者报告的结果相似。

结论

在这项接受 3mg/kg 依匹单抗治疗的真实世界患者人群中,进行了≥3 年的长期随访,安全性和 OS 与临床试验报告的结果一致。研究期间患者报告的生活质量得到维持。在初治和既往治疗患者的 OS 分析中,提示依匹单抗在早期治疗中有获益作用。

试验注册

ClinicalTrials.gov,NCT01511913。2012 年 1 月 19 日注册-回顾性注册,https://clinicaltrials.gov/ct2/show/NCT01511913。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8904/8164785/26f11546ae6f/12885_2021_8032_Fig1_HTML.jpg

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