Patient‐reported outcomes in a phase 2 study comparing atezolizumab alone or with bevacizumab vs sunitinib in previously untreated metastatic renal cell carcinoma

阿替唑单抗 舒尼替尼 医学 贝伐单抗 肾细胞癌 内科学 肿瘤科 危险系数 耐受性 临床研究阶段 置信区间 泌尿科 癌症 不利影响 化疗 无容量 免疫疗法
作者
Sumanta K. Pal,David F. McDermott,Michael B. Atkins,Bernard Escudier,Brian I. Rini,Robert J. Motzer,Lawrence Fong,Richard W. Joseph,Stéphane Oudard,Alain Ravaud,Sergio Bracarda,Cristina Suárez,Elaine T. Lam,Toni K. Choueiri,Beiying Ding,Caroleen Quach,Kenji Hashimoto,Christina Schiff,Elisabeth Piault‐Louis,Thomas Powles
出处
期刊:BJUI [Wiley]
卷期号:126 (1): 73-82 被引量:19
标识
DOI:10.1111/bju.15058
摘要

Objective To evaluate patient‐reported outcome (PRO) data from the IMmotion150 study. The phase 2 IMmotion150 study showed improved progression‐free survival with atezolizumab plus bevacizumab vs sunitinib in patients with programmed death‐ligand 1 (PD‐L1)+ tumours and suggested activity of atezolizumab monotherapy in previously untreated metastatic renal cell carcinoma (mRCC). Patients and methods Patients with previously untreated mRCC were randomised to atezolizumab 1200 mg intravenously (i.v.) every 3 weeks ( n = 103), the atezolizumab regimen plus bevacizumab 15 mg/kg i.v. every 3 weeks ( n = 101), or sunitinib 50 mg orally daily (4 weeks on, 2 weeks off; n = 101). The MD Anderson Symptom Inventory (MDASI) and Brief Fatigue Inventory (BFI) were administered on days 1 and 22 of each 6‐week cycle. Time to deterioration (TTD), change from baseline in MDASI core and RCC symptom severity, interference with daily life, and BFI fatigue severity and interference scores were reported for all comers. The TTD was the first ≥2‐point score increase over baseline. Absolute effect size ≥0.2 suggested a clinically important difference with checkpoint inhibitor therapy vs sunitinib. Results Completion rates were >90% at baseline and ≥80% at most visits. Delayed TTD in core and RCC symptoms, symptom interference, fatigue, and fatigue‐related interference was observed with atezolizumab (both alone and in combination) vs sunitinib. Improved TTD (hazard ratio [HR], 95% confidence interval [CI]) was more pronounced with atezolizumab monotherapy: core symptoms, 0.39 (0.22–0.71); RCC symptoms, 0.22 (0.12–0.41); and symptom interference, 0.36 (0.22–0.58). Change from baseline by visit, evaluated by the MDASI, also showed a trend favouring atezolizumab monotherapy vs sunitinib. Small sample sizes may have limited the ability to draw definitive conclusions. Conclusion PROs suggested that atezolizumab alone or with bevacizumab maintained daily function compared with sunitinib. Notably, symptoms were least severe with atezolizumab alone vs sunitinib (IMmotion150; ClinicalTrials.gov Identifier: NCT01984242).
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
2秒前
瘪良科研完成签到,获得积分10
2秒前
研友_Lw4Ngn发布了新的文献求助10
3秒前
852应助跳跃碧灵采纳,获得10
4秒前
脑洞疼应助cc采纳,获得10
4秒前
6秒前
善学以致用应助shelly采纳,获得10
7秒前
10秒前
山楂完成签到,获得积分10
11秒前
12秒前
酷炫钥匙完成签到,获得积分10
12秒前
hdy331完成签到,获得积分10
12秒前
13秒前
15秒前
隐形曼青应助xr采纳,获得10
15秒前
光亮面包完成签到 ,获得积分10
15秒前
山楂发布了新的文献求助10
15秒前
zw99完成签到,获得积分10
16秒前
123发布了新的文献求助10
17秒前
酷炫钥匙发布了新的文献求助10
17秒前
17秒前
17秒前
Frozen完成签到,获得积分10
18秒前
科研通AI2S应助eplision采纳,获得10
18秒前
奥利奥完成签到,获得积分10
19秒前
搜集达人应助研友_Lw4Ngn采纳,获得10
19秒前
不动僧发布了新的文献求助10
19秒前
liuHX发布了新的文献求助10
20秒前
23秒前
23秒前
Ying发布了新的文献求助10
24秒前
大旭完成签到 ,获得积分10
25秒前
gcm完成签到 ,获得积分10
25秒前
赐我一只喵完成签到,获得积分20
27秒前
27秒前
搬砖的化学男应助山楂采纳,获得10
28秒前
cosmtraveller发布了新的文献求助10
29秒前
shelly发布了新的文献求助10
29秒前
orixero应助Elian采纳,获得10
30秒前
30秒前
高分求助中
Sustainability in Tides Chemistry 2000
Bayesian Models of Cognition:Reverse Engineering the Mind 800
Essentials of thematic analysis 700
A Dissection Guide & Atlas to the Rabbit 600
Very-high-order BVD Schemes Using β-variable THINC Method 568
Внешняя политика КНР: о сущности внешнеполитического курса современного китайского руководства 500
Revolution und Konterrevolution in China [by A. Losowsky] 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3124564
求助须知:如何正确求助?哪些是违规求助? 2774883
关于积分的说明 7724421
捐赠科研通 2430307
什么是DOI,文献DOI怎么找? 1291057
科研通“疑难数据库(出版商)”最低求助积分说明 622052
版权声明 600297