Outcomes associated with immune-related adverse events in metastatic non-small cell lung cancer treated with nivolumab: a pooled exploratory analysis from a global cohort

被引:76
|
作者
Naqash, Abdul Rafeh [1 ,7 ]
Ricciuti, Biagio [2 ,3 ]
Owen, Dwight H. [4 ]
Florou, Vaia [5 ,10 ]
Toi, Yukihiro [6 ]
Cherry, Cynthia [1 ,7 ]
Hafiz, Maida [8 ]
De Giglio, Andrea [2 ]
Muzaffar, Mavish [7 ]
Patel, Sandip H. [4 ]
Sugawara, Shunichi [6 ]
Burkart, Jarred [4 ]
Park, Wungki [5 ,9 ]
Chiari, Rita [2 ]
Sugisaka, Jun [6 ]
Otterson, Gregory A. [4 ]
de Lima Lopes, Gilberto [5 ]
Walker, Paul R. [7 ]
机构
[1] NCI, Div Canc Treatment & Diag, Dev Therapeut Clin, Bldg 31-3A44,31 Ctr Dr, Bethesda, MD 20892 USA
[2] Univ Perugia, Thorac Oncol Unit, Santa Maria Della Misericordia Hosp, Perugia, Italy
[3] Dana Farber Canc Inst, Lowe Ctr Thorac Oncol, Boston, MA 02115 USA
[4] Ohio State Univ, Dept Internal Med, Div Med Oncol, Columbus, OH 43210 USA
[5] Univ Miami, Miller Sch Med, Div Oncol, Dept Med, Miami, FL 33136 USA
[6] Sendai Kousei Hosp, Dept Pulm Med, Aoba Ku, Hirosemachi, Sendai, Miyagi, Japan
[7] East Carolina Univ, Div Hematol Oncol, Dept Internal Med, Greenville, NC 27858 USA
[8] East Carolina Univ, Dept Pulm Med, Greenville, NC 27858 USA
[9] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[10] Univ Utah, Div Med Oncol, Huntsman Canc Inst, Salt Lake City, UT USA
关键词
Immune checkpoint inhibition; Nivolumab; Immune-related adverse events; Pneumonitis; ICI discontinuation; AUTOIMMUNITY;
D O I
10.1007/s00262-020-02536-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Immune-related adverse events (irAEs) comprise a distinct spectrum of auto-inflammatory manifestations triggered due to immune checkpoint inhibitors (ICI). Current data on the association of irAEs with outcomes in NSCLC treated with nivolumab are limited. Methods and objectives We pooled data from 531 metastatic NSCLC patients from five centers treated with nivolumab after failing platinum-based chemotherapy. The primary objective was to investigate the relationship between irAEs with clinical benefit to nivolumab as well as to elucidate patterns of irAE-related ICI discontinuations and their impact on survival. Results 33.0% (173/531) of patients treated with nivolumab were noted to have an irAE. Patients with irAEs had a significantly longer median PFS [6.1 vs. 3.1 months, HR 0.68 95% CI (0.55-0.85); p = 0.001] and OS [14.9 vs. 7.4 months, HR 0.66 95% CI (0.52-0.82); p < 0.001)] compared to those without irAEs. In multivariate analysis, the presence of irAEs showed a significantly better PFS [HR 0.69, 95% CI (0.55-0.87); p = 0.002] and a trend for better OS [HR 0.62, 95% CI (0.55-1.03); p = 0.057]. Patients with permanent ICI discontinuation secondary to index irAE had a significantly shorter median PFS [2.3 vs. 6.6 months, HR 1.74 95% CI (1.06-2.80); p = 0.02] and median OS [3.6 vs. 17.6 months; HR 2.61 95% CI (1.61-4.21); p < 0.001] compared to those that did not have permanent ICI discontinuation. Conclusions Our pooled exploratory analysis demonstrates improved clinical benefit to nivolumab in NSCLC patients experiencing irAEs. We also observed negative impact of irAE-related treatment discontinuation on survival in this group of patients.
引用
收藏
页码:1177 / 1187
页数:11
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