Efficacy and Safety of Paclitaxel-Based PD-1/PD-L1 Immunotherapies for Triple-Negative Breast Cancer: A Systematic Review and Network Meta-Analysis

阿替唑单抗 三阴性乳腺癌 紫杉醇 杜瓦卢马布 医学 肿瘤科 乳腺癌 危险系数 内科学 不利影响 免疫疗法 癌症 彭布罗利珠单抗 置信区间
作者
Youran Dai,Tao Ruan,Wenhui Yang,Shan Liu,Jiahao Chen,Yingying Fang,Qiushuang Li
出处
期刊:Clinical Medicine: Oncology [SAGE Publishing]
卷期号:18
标识
DOI:10.1177/11795549241308072
摘要

Background: Triple negative breast cancer (TNBC) is a deadly subtype of breast cancer with limited treatment options. Currently, programmed death 1 (PD-1)/programmed death ligand 1 (PD-L1) inhibitors have become the first choice for breast cancer immunotherapies. Despite paclitaxel being considered a cornerstone drug in breast cancer treatment, the effectiveness, safety, and optimal drug selection for its combination with PD-1/PD-L1 inhibitors remain uncertain. Methods: We conducted a systematic review and network meta-analysis, performing a comprehensive literature search across PubMed, Embase, and the Cochrane Library from the inception of each database through May 18, 2024. Selected trials were those that assessed the efficacy and safety of paclitaxel-based PD-1/PD-L1 therapies for the treatment of TNBC. The primary endpoint assessed was overall survival (OS), while secondary outcomes included progression-free survival (PFS), adverse events (AEs), overall response rate (ORR), and Pathological complete response (pCR). This study is registered in PROSPERO under registration number CRD42023429651. Results: A total of 8 RCTs meeting our eligibility criteria were included, involving 4626 patients who received either Paclitaxel (Paclitaxel-placebo/chemotherapy) or a combination of durvalumab, pembrolizumab, atezolizumab, toripalimab with paclitaxel. The pooled results demonstrated that Durvalumab combined with Paclitaxel significantly reduced the hazard ratio for OS (surface under the cumulative ranking [SUCRA]: 91.05%) and PFS compared with Paclitaxel alone (SUCRA: 83.52%). Additionally, Durvalumab plus Paclitaxel significantly improved the ORR compared with Paclitaxel (odds ratio [OR]: 2.30; 95% credible interval [CrI]: 1.10–5.20). For safety outcomes, Atezolizumab plus Paclitaxel showed a favorable profile in AEs, with no significant differences observed between groups. In the pCR study, Pembrolizumab plus Paclitaxel was the most effective treatment option (SUCRA: 81.85%). Conclusions: When combined with paclitaxel, PD-1/PD-L1 inhibitors exhibit a favorable survival benefit. The combination of Durvalumab and paclitaxel represents the optimal treatment option. In the future, attention should be paid to the TNBC subtypes and drug dosage, as these factors may help to design personalized TNBC treatment programs.
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
PDF的下载单位、IP信息已删除 (2025-6-4)

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
量子星尘发布了新的文献求助10
2秒前
4秒前
怕孤单的从灵完成签到 ,获得积分10
5秒前
5秒前
顾矜应助ruqayyah采纳,获得30
7秒前
7秒前
醉熏的行云完成签到 ,获得积分10
8秒前
FashionBoy应助momucy采纳,获得10
8秒前
10秒前
13秒前
慕青应助鳗鱼中心采纳,获得10
14秒前
15秒前
17秒前
天天快乐应助misa采纳,获得20
17秒前
17秒前
毛竹完成签到,获得积分10
19秒前
20秒前
20秒前
天坑专业战神完成签到,获得积分10
20秒前
21秒前
22秒前
吃的饭广泛应助神勇的荟采纳,获得10
23秒前
慕青应助纯真沛儿采纳,获得20
24秒前
知知发布了新的文献求助10
24秒前
ruqayyah发布了新的文献求助30
25秒前
fuje发布了新的文献求助10
26秒前
鳗鱼中心发布了新的文献求助10
26秒前
量子星尘发布了新的文献求助10
27秒前
29秒前
30秒前
31秒前
请问哈完成签到 ,获得积分10
33秒前
小魏完成签到,获得积分20
33秒前
李健应助知知采纳,获得10
34秒前
34秒前
方忆丹完成签到,获得积分10
35秒前
35秒前
小二郎应助薛薛薛采纳,获得50
36秒前
36秒前
张博洋发布了新的文献求助10
36秒前
高分求助中
(禁止应助)【重要!!请各位详细阅读】【科研通的精品贴汇总】 10000
Plutonium Handbook 4000
International Code of Nomenclature for algae, fungi, and plants (Madrid Code) (Regnum Vegetabile) 1500
Functional High Entropy Alloys and Compounds 1000
Building Quantum Computers 1000
Social Epistemology: The Niches for Knowledge and Ignorance 500
优秀运动员运动寿命的人文社会学因素研究 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 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 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 4227062
求助须知:如何正确求助?哪些是违规求助? 3760675
关于积分的说明 11821115
捐赠科研通 3421655
什么是DOI,文献DOI怎么找? 1877841
邀请新用户注册赠送积分活动 931059
科研通“疑难数据库(出版商)”最低求助积分说明 838961