A quality-adjusted time without symptoms and toxicity (Q-TWiST) analysis comparing nivolumab plus ipilimumab or nivolumab plus chemotherapy versus chemotherapy in patients with advanced esophageal squamous-cell carcinoma in CheckMate 648

I. Chau , J. Bridgewater , L. Wyrwicz , M. Greenwood , S.I. Blum , A. Moreno-Koehler , E. Martin , F. Taylor , C. Davis , P. Singh
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Abstract

Background

First-line nivolumab plus chemotherapy (NIVO + CHEMO) and nivolumab plus ipilimumab (NIVO + IPI) improves overall survival for patients with advanced esophageal squamous-cell carcinoma (ESCC). This analysis aimed to use quality-adjusted time without symptoms or toxicity (Q-TWiST) analyses to assess the overall risk–benefit profile of these treatments in the CheckMate 648 study.

Materials and methods

A post hoc analysis of CheckMate 648 assessed the association of quality-adjusted survival with treatment types (first-line NIVO + CHEMO, NIVO + IPI, or CHEMO alone) using the Q-TWiST methodology. The analysis included all randomized patients and those with tumor cell programmed death-ligand 1 (PD-L1) ≥1% at baseline, with a minimum follow-up of 45 months. Health-related quality of life was assessed using the EuroQoL 5-Dimension 3-Level (EQ-5D-3L) questionnaire. Differences in Q-TWiST exceeding 1.5 months were deemed clinically important.

Results

The analysis included 970 patients in the all-randomized population. Q-TWiST values were 12.8 and 12.9 months for NIVO + CHEMO and NIVO + IPI, respectively, compared with 10.8 months for CHEMO alone, showing gains of 2.0 and 2.1 months, respectively. In patients with tumor cell PD-L1 ≥1% (473 patients), Q-TWiST values were higher for NIVO + CHEMO (13.0 months) and NIVO + IPI (13.3 months) compared with CHEMO alone (9.1 months), with gains of 3.9 and 4.2 months, respectively. All gains surpassed the clinically important threshold.

Conclusion

These findings support NIVO + CHEMO and NIVO + IPI as first-line treatments for patients with advanced ESCC, particularly those with tumor cell PD-L1 ≥1%.
一项质量调整无症状和毒性时间(Q-TWiST)分析,比较了CheckMate 648中晚期食管鳞状细胞癌患者的纳武单抗加易普利单抗或纳武单抗加化疗与化疗
一线纳武单抗加化疗(NIVO + CHEMO)和纳武单抗加伊匹单抗(NIVO + IPI)可改善晚期食管鳞状细胞癌(ESCC)患者的总生存期。该分析旨在使用质量调整无症状或毒性时间(Q-TWiST)分析来评估CheckMate 648研究中这些治疗的总体风险-收益概况。材料和方法对CheckMate 648进行事后分析,使用Q-TWiST方法评估了质量调整生存率与治疗类型(一线NIVO + CHEMO, NIVO + IPI或单独化疗)的关系。该分析包括所有随机患者和基线时肿瘤细胞程序性死亡-配体1 (PD-L1)≥1%的患者,至少随访45个月。健康相关生活质量采用EuroQoL 5维3级(EQ-5D-3L)问卷进行评估。超过1.5个月的Q-TWiST差异被认为具有临床重要性。结果纳入全随机人群970例患者。NIVO + CHEMO和NIVO + IPI组的Q-TWiST值分别为12.8和12.9个月,而单独化疗组的Q-TWiST值为10.8个月,分别为2.0和2.1个月。在肿瘤细胞PD-L1≥1%的患者(473例)中,NIVO + CHEMO(13.0个月)和NIVO + IPI(13.3个月)的Q-TWiST值高于单纯化疗(9.1个月),分别增加3.9个月和4.2个月。所有的收益都超过了临床重要的阈值。结论:这些研究结果支持NIVO + CHEMO和NIVO + IPI作为晚期ESCC患者的一线治疗方案,特别是肿瘤细胞PD-L1≥1%的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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