Incidence of Pneumonitis With Use of Programmed Death 1 and Programmed Death-Ligand 1 Inhibitors in Non-Small Cell Lung Cancer

被引:423
作者
Khunger, Monica [1 ]
Rakshit, Sagar [1 ]
Pasupuleti, Vinay [4 ]
Hernandez, Adrian V. [5 ,6 ]
Mazzone, Peter [2 ]
Stevenson, James [3 ]
Pennell, Nathan A. [3 ]
Velcheti, Vamsidhar [3 ]
机构
[1] Cleveland Clin, Dept Internal Med, Cleveland, OH 44195 USA
[2] Cleveland Clin, Res Inst, Cleveland, OH 44195 USA
[3] Cleveland Clin, Dept Hematol & Oncol, Tausig Canc Inst, Cleveland, OH 44195 USA
[4] Case Western Reserve Univ, Dept Biostat, Cleveland, OH 44106 USA
[5] Univ Connecticut, Hartford Hosp Evidence Based Practice Ctr, Hartford, CT 06112 USA
[6] Univ Peruana Ciencias Aplicadas UPC, Sch Med, Lima, Peru
关键词
immune-related adverse events; immunotherapy; meta-analysis; non-small cell lung cancer; pneumonitis; AVELUMAB MSB0010718C; ANTI-PD-L1; ANTIBODY; 1ST-LINE TREATMENT; OPEN-LABEL; PHASE-II; NIVOLUMAB; DOCETAXEL; SAFETY; ATEZOLIZUMAB; TRIAL;
D O I
10.1016/j.chest.2017.04.177
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
BACKGROUND: Programmed death 1 (PD-1) programmed death-ligand 1 (PD-L1) inhibitors show significant clinical activity in non-small cell lung carcinoma (NSCLC). However, they are often associated with potentially fatal immune-mediated pneumonitis. Preliminary reports of trials suggest a difference in the rate of pneumonitis with PD-1 and PD-L1 inhibitors. We sought to determine the overall incidence of pneumonitis and differences according to type of inhibitors and prior chemotherapy use. METHODS: MEDLINE, Embase, and Scopus databases were searched up to November 2016. Rates of pneumonitis of any grade and grade >= 3 from all clinical trials investigating nivolumab, pembrolizumab, atezolizumab, durvalumab, and avelumab as single agents in NSCLC were collected. The incidence of pneumonitis across trials was calculated using DerSimonian-Laird random effects models. We compared incidences between PD-1 and PD-L1 inhibitors and between treatment naive and previously treated patients. RESULTS: Nineteen trials (12 with PD-1 inhibitors [n = 3,232] and 7 with PD-L1 inhibitors [n = 1,806]) were identified. PD-1 inhibitors were found to have statistically significant higher incidence of any grade pneumonitis compared with PD-L1 inhibitors (3.6%; 95% CI, 2.4%4.9% vs 1.3%; 95% CI, 0.8%-1.9%, respectively; P =.001). PD-1 inhibitors were also associated with higher incidence of grade 3 or 4 pneumonitis (1.1%; 95% CI, 0.6%-1.7% vs 0.4%; 95% CI, 0%-0.8%; P =.02). Treatment naive patients had higher incidence of grade 1 through 4 pneumonitis compared with previously treated patients (4.3%; 95% CI, 2.4%-6.3% vs 2.8%; 95% CI, 1.7%-4%; P =.03). CONCLUSIONS: There was a higher incidence of pneumonitiswith use of PD-1 inhibitors compared with PD-L1 inhibitors. Higher rate of pneumonitis was more common in treatment naive patients.
引用
收藏
页码:271 / 281
页数:11
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