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III 期 HIMALAYA 研究中 Tremelimumab 联合 Durvalumab 在不可切除肝细胞癌中的患者报告结局。

Patient-Reported Outcomes From the Phase III HIMALAYA Study of Tremelimumab Plus Durvalumab in Unresectable Hepatocellular Carcinoma.

机构信息

Liver Unit and HPB Oncology Area, Clínica Universidad de Navarra and CIBEREHD, Pamplona, Spain.

University Medical Center, Mainz, Germany.

出版信息

J Clin Oncol. 2024 Aug 10;42(23):2790-2799. doi: 10.1200/JCO.23.01462. Epub 2024 May 28.

Abstract

PURPOSE

In the phase III HIMALAYA study (ClinicalTrials.gov identifier: NCT03298451) in unresectable hepatocellular carcinoma (uHCC), the Single Tremelimumab Regular Interval Durvalumab (STRIDE) regimen significantly improved overall survival versus sorafenib, and durvalumab monotherapy was noninferior to sorafenib. Patient-reported outcomes (PROs), a secondary outcome from HIMALAYA, are reported here.

METHODS

Participants were randomly assigned to receive STRIDE, durvalumab, or sorafenib. PROs were assessed (preplanned secondary outcome) using the European Organization for Research and Treatment of Cancer 30-item Quality of Life Questionnaire and the 18-item HCC module. Time to deterioration (TTD), change from baseline and improvement rate in global health status/quality of life (GHS/QoL), functioning, and disease-related symptoms were analyzed.

RESULTS

In total, 1,171 participants were randomly assigned to STRIDE (n = 393), durvalumab (n = 389), or sorafenib (n = 389) and were evaluable for PRO assessments. Across treatment arms, compliance rates for PROs were >77% at baseline and >70% overall. Baseline scores were comparable across treatment arms. TTD in GHS/QoL, physical functioning, fatigue, appetite loss, and abdominal pain was numerically longer for both STRIDE and durvalumab versus sorafenib. Clinically meaningful deterioration in PROs was not observed in any treatment arm. However, TTD in nausea and abdominal swelling was numerically longer for STRIDE versus sorafenib, and the likelihood of clinically meaningful improvement in GHS/QoL, role, emotional and social functioning, and disease-related symptoms was greater with STRIDE and durvalumab versus sorafenib. PROs with STRIDE and durvalumab were generally similar.

CONCLUSION

Compared with sorafenib, STRIDE and durvalumab were associated with clinically meaningful, patient-centered GHS/QoL, functioning, and symptom benefits in people with uHCC. These findings support the benefits of the STRIDE regimen compared with sorafenib for a diverse population reflective of the global uHCC population.

摘要

目的

在 III 期 HIMALAYA 研究(ClinicalTrials.gov 标识符:NCT03298451)中,对于不可切除的肝细胞癌(uHCC),单一 Tremelimumab 常规间隔度伐利尤单抗(STRIDE)方案显著改善了总生存期,优于索拉非尼,且度伐利尤单抗单药治疗不劣于索拉非尼。现将 HIMALAYA 的次要终点患者报告结局(PROs)报告如下。

方法

参与者被随机分配接受 STRIDE、度伐利尤单抗或索拉非尼治疗。使用欧洲癌症研究与治疗组织 30 项生活质量问卷和 18 项 HCC 模块(preplanned secondary outcome)评估 PROs。分析从基线恶化时间(TTD)、全球健康状况/生活质量(GHS/QoL)、功能和疾病相关症状的变化以及改善率。

结果

共有 1171 名参与者被随机分配至 STRIDE(n = 393)、度伐利尤单抗(n = 389)或索拉非尼(n = 389)组,且可用于 PRO 评估。在所有治疗组中,基线时 PROs 的依从率>77%,总体>70%。治疗组之间基线评分相当。在 GHS/QoL、身体功能、疲劳、食欲减退和腹痛方面,STRIDE 和度伐利尤单抗的 TTD 均长于索拉非尼。任何治疗组均未观察到 PRO 出现有临床意义的恶化。然而,STRIDE 的 TTD 在恶心和腹部肿胀方面长于索拉非尼,且与索拉非尼相比,STRIDE 和度伐利尤单抗在 GHS/QoL、角色、情绪和社会功能以及疾病相关症状方面更有可能出现有临床意义的改善。STRIDE 和度伐利尤单抗的 PRO 大致相似。

结论

与索拉非尼相比,STRIDE 和度伐利尤单抗在不可切除 HCC 患者中与具有临床意义的以患者为中心的 GHS/QoL、功能和症状改善相关。这些发现支持与索拉非尼相比,STRIDE 方案在反映全球 uHCC 人群的多样化人群中的获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fcd/11315407/c5bd07225961/jco-42-2790-g001.jpg

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