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在转移性葡萄膜黑色素瘤中,替贝福单抗是否优于联合免疫检查点阻断及其他全身治疗?一项进行了人群校正的疗效对比分析。

Is tebentafusp superior to combined immune checkpoint blockade and other systemic treatments in metastatic uveal melanoma? A comparative efficacy analysis with population adjustment.

作者信息

Petzold Anne, Steeb Theresa, Wessely Anja, Koch Elias A T, Vera Julio, Berking Carola, Heppt Markus V

机构信息

Department of Dermatology, Uniklinikum Erlangen, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Erlangen, Germany; Comprehensive Cancer Center Erlangen-European Metropolitan Area of Nuremberg (CCC ER-EMN), Erlangen, Germany; Deutsches Zentrum Immuntherapie (DZI), Uniklinikum Erlangen, Erlangen, Germany.

出版信息

Cancer Treat Rev. 2023 Apr;115:102543. doi: 10.1016/j.ctrv.2023.102543. Epub 2023 Mar 13.

Abstract

BACKGROUND

Distinct systemic treatments exist for metastatic uveal melanoma. Tebentafusp and combined immune checkpoint blockade (ICB) with ipilimumab plus anti-PD-1 antibodies are the most commonly used treatment options but their comparative efficacy is unclear. The aim of this study is to compare currently available systemic treatments regarding overall survival (OS) and progression-free survival (PFS) with a focus on the comparison of tebentafusp versus combined ICB.

METHODS

The protocol for this study was defined a priori and registered online in the PROSPERO international prospective register of systematic reviews (CRD42022308356, date of registration: 7.2.2022). We performed a systematic literature search in Medline, Embase, and Central to identify eligible studies reporting Kaplan-Meier curves or individual-level survival data showing OS and PFS for metastatic uveal melanoma patients treated with systemic treatments. Kaplan-Meier curves were digitized using the "WebPlotDigitizer" program. Individual-level survival data were subsequently remodelled and pooled for distinct treatment groups. To compare the OS of tebentafusp versus combined ICB, we used matching-adjusted indirect comparison (MAIC), two-stage MAIC (2SMAIC), and simulated treatment comparison (STC) together with digitized individual-level survival data as population-adjusted models.

RESULTS

Overall, 55 independent studies were included of which 2,682 patients were evaluable for OS and 2,258 for PFS. Tebentafusp showed the highest median OS (mOS) of 22.4 months (95% confidence interval (CI): 19.9-29.6) compared to combined ICB (mOS: 15.7 months (95% CI: 14.4-17.9)), anti-PD-(L)1 antibody (mOS: 10.9 months (95% CI: 9.8-13.4)), chemotherapy (mOS: 9.95 months (95% CI: 8.9-11.2)), targeted therapies (mOS: 8.86 months (95% CI: 7.5-10.8)), and anti-CTLA-4 antibody (mOS: 7.8 months (95% CI: 6.8-9.3). The median PFS (mPFS) was similar among the treatment groups ranging from 2.7 months to 3.4 months. For the comparison of tebentafusp versus combined ICB, the hazard ratio (HR) was 0.641 (95% CI: 0.449-0.915) in the unadjusted model, whereas the population-adjusted models showed a HR of 0.386 (95% CI: 0.236-0.631) using MAIC, 0.378 (95% CI: 0.234-0.612) applying 2SMAIC and 0.284 (95% CI: 0.184-0.440) using STC.

CONCLUSIONS

Tebentafusp achieved the best results compared to combined ICB and other systemic treatments, although these results have to be interpreted with caution due to the approximative methodical approach and high heterogeneity of included studies.

摘要

背景

转移性葡萄膜黑色素瘤有多种不同的全身治疗方法。替贝福单抗以及将免疫检查点阻断(ICB)与伊匹木单抗加抗PD - 1抗体联合使用是最常用的治疗选择,但它们的相对疗效尚不清楚。本研究的目的是比较目前可用的全身治疗方法在总生存期(OS)和无进展生存期(PFS)方面的差异,重点是比较替贝福单抗与联合ICB。

方法

本研究方案预先确定,并在PROSPERO国际系统评价前瞻性注册库(CRD42022308356,注册日期:2022年2月7日)在线注册。我们在Medline、Embase和CENTRAL中进行了系统的文献检索,以识别符合条件的研究,这些研究报告了接受全身治疗的转移性葡萄膜黑色素瘤患者的Kaplan - Meier曲线或显示OS和PFS的个体水平生存数据。使用“WebPlotDigitizer”程序将Kaplan - Meier曲线数字化。随后对个体水平的生存数据进行重塑,并汇总到不同的治疗组中。为了比较替贝福单抗与联合ICB的OS,我们使用匹配调整间接比较(MAIC)、两阶段MAIC(2SMAIC)和模拟治疗比较(STC),并将数字化的个体水平生存数据用作总体调整模型。

结果

总体而言,纳入了55项独立研究,其中2682例患者可评估OS,2258例可评估PFS。与联合ICB(中位OS:15.7个月(95%置信区间(CI):14.4 - 17.9))、抗PD - (L)1抗体(中位OS:10.9个月(95% CI:9.8 - 13.4))、化疗(中位OS:9.95个月(95% CI:8.9 - 11.2))、靶向治疗(中位OS:8.86个月(95% CI:7.5 - 10.8))和抗CTLA - 4抗体(中位OS:7.8个月(95% CI:6.8 - 9.3))相比,替贝福单抗的中位OS最高,为22.4个月(95% CI:19.9 - 29.6)。各治疗组的中位PFS(mPFS)相似,范围为2.7个月至3.4个月。在替贝福单抗与联合ICB的比较中,未调整模型中的风险比(HR)为0.641(95% CI:0.449 - 0.915),而总体调整模型使用MAIC时HR为0.386(95% CI:0.236 - 0.631),应用2SMAIC时为0.378(95% CI:0.234 - 0.612),使用STC时为0.284(95% CI:0.184 - 0.440)。

结论

与联合ICB和其他全身治疗相比,替贝福单抗取得了最佳结果,尽管由于方法学方法近似且纳入研究的异质性高,这些结果必须谨慎解读。

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