Predictive value of PD-L1 and other clinical factors for chemoimmunotherapy in advanced non-small-cell lung cancer

被引:7
作者
Woodford, Rachel [1 ]
Loh, Yanni [1 ]
Lee, Joanna [1 ]
Cooper, Wendy [2 ,3 ,4 ]
Marschner, Ian [5 ,6 ]
Lewis, Craig R. [7 ]
Millward, Michael [8 ,9 ]
Lord, Sally [5 ,10 ]
Gralla, Richard J. [11 ]
Yang, James C-H [12 ,13 ]
Mok, Tony [14 ]
Lee, Chee K. [1 ,5 ]
机构
[1] St George Hosp, Canc Care Ctr, Sydney, NSW 2217, Australia
[2] Royal Prince Alfred Hosp, Tissue Pathol & Diagnost Oncol, Sydney, NSW 2050, Australia
[3] Univ Sydney, Sydney Med Sch, Sydney, NSW 2006, Australia
[4] Western Sydney Univ, Sch Med, Sydney, NSW 2751, Australia
[5] Univ Sydney, Natl Hlth & Med Res Council, Clin Trials Ctr, Sydney, NSW 1450, Australia
[6] Macquarie Univ, Dept Stat, Sydney, NSW 2109, Australia
[7] Univ NSW, Prince Wales Hosp, Clin Sch, Sydney, NSW 2031, Australia
[8] Univ Western Australia, Sch Med, Perth, WA 6009, Australia
[9] Sir Charles Gairdner Hosp, Dept Med Oncol, Perth, WA 6010, Australia
[10] Univ Notre Dame, Sch Med, Sydney, NSW 2010, Australia
[11] Albert Einstein Coll Med, Jacobi Med Ctr, Bronx, NY 10461 USA
[12] Natl Taiwan Univ, Grad Inst Oncol, Taipei 10002, Taiwan
[13] Natl Taiwan Univ Hosp, Dept Oncol, Taipei 10002, Taiwan
[14] Chinese Univ Hong Kong, Hong Kong Canc Inst, Dept Clin Oncol, Shatin, Hong Kong, Peoples R China
关键词
chemoimmunotherapy; meta-analysis; non-small-cell lung cancer; PD-L1; expression; progression-free survival; AMERICAN SOCIETY; SQUAMOUS-CELL; OPEN-LABEL; NIVOLUMAB; CHEMOTHERAPY; DOCETAXEL; IMMUNOHISTOCHEMISTRY; PEMBROLIZUMAB; MECHANISMS; PHASE-1;
D O I
10.2217/fon-2019-0105
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We investigate if PD-L1 expression and other clinical characteristics predict chemoimmunotherapy (CIT) benefits versus chemotherapy in advanced non-small-cell lung cancer. We performed a meta-analysis of randomized controlled trials of CIT versus chemotherapy identified through electronic searches. In seven randomized controlled trials (n =4170), CIT prolonged progression-free survival over chemotherapy (hazard ratio [HR]: 0.62; 95% CI: 0.58-0.67; p < 0.00001). The treatment benefits differed between PD-L1-high (HR: 0.41; 95% CI: 0.34-0.49) and PD-L1 low (HR: 0.63; 95% CI: 0.55-0.72; interaction-p = 0.00002) and PD-L1-high and PD-L1-negative (HR: 0.72; 95% CI: 0.65-0.80; interaction-p < 0.00001). Similar benefits were observed regardless of gender, EGFR/ALK status and histological subtype. PD-L1 status is predictive of CIT benefit and may assist patient selection and design of future trials.
引用
收藏
页码:2371 / 2383
页数:13
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