Impact of TMB/PD-L1 expression and pneumonitis on chemoradiation and durvalumab response in stage III NSCLC

被引:17
作者
Alessi, Joao V. V. [1 ]
Ricciuti, Biagio [1 ]
Wang, Xinan [2 ]
Pecci, Federica [1 ]
Di Federico, Alessandro [1 ]
Lamberti, Giuseppe [1 ]
Elkrief, Arielle [3 ,4 ,5 ]
Rodig, Scott J. J. [6 ,7 ]
Lebow, Emily S. S.
Eicholz, Jordan E. E.
Thor, Maria [9 ]
Rimner, Andreas [8 ]
Schoenfeld, Adam J. J.
Chaft, Jamie E. E.
Johnson, Bruce E. E.
Gomez, Daniel R. R.
Awad, Mark M. M.
Shaverdian, Narek [8 ]
机构
[1] Dana Farber Canc Inst, Lowe Ctr Thorac Oncol, Boston, MA USA
[2] Harvard Univ, Harvard TH Chan Sch Publ Hlth, Dept Environm Hlth, Boston, MA USA
[3] Mem Sloan Kettering Canc Ctr, Thorac Oncol Serv, New York, NY USA
[4] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY USA
[5] Mem Sloan Kettering Canc Ctr, Human Oncol & Pathogenesis Program, few York, NY USA
[6] Brigham & Womens Hosp, ImmunoProfile, Boston, MA USA
[7] Brigham & Womens Hosp, Dept Pathol, Boston, MA USA
[8] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, New York, NY 10065 USA
[9] Mem Sloan Kettering Canc Ctr, Dept Med Phys, New York, NY USA
关键词
CELL LUNG-CANCER; T-CELLS; CHEMORADIOTHERAPY; PEMBROLIZUMAB; BLOCKADE; EFFICACY; OUTCOMES; THERAPY; PD-L1;
D O I
10.1038/s41467-023-39874-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Concurrent chemoradiation and durvalumab is standard of care for stage III non-small cell lung cancer, however, efficacy is variable. Here, the authors show PD-L1 tumor proportion score expression and increased tumor mutational burden are predictive of response and that early-onset pneumonitis leading to durvalumab discontinuation is associated with poor survival. Although concurrent chemoradiation (CRT) and durvalumab consolidation has become a standard treatment for stage III non-small cell lung cancer (NSCLC), clinicopathologic and genomic factors associated with its efficacy remain poorly characterized. Here, in a multi-institutional retrospective cohort study of 328 patients treated with CRT and durvalumab, we identify that very high PD-L1 tumor proportion score (TPS) expression ( & GE; 90%) and increased tumor mutational burden (TMB) are independently associated with prolonged disease control. Additionally, we identify the impact of pneumonitis and its timing on disease outcomes among patients who discontinue durvalumab: compared to patients who experienced early-onset pneumonitis ( < 3 months) leading to durvalumab discontinuation, patients with late-onset pneumonitis had a significantly longer PFS (12.7 months vs not reached; HR 0.24 [95% CI, 0.10 to 0.58]; P = 0.001) and overall survival (37.2 months vs not reached; HR 0.26 [95% CI, 0.09 to 0.79]; P = 0.017). These findings suggest that opportunities exist to improve outcomes in patients with lower PD-L1 and TMB levels, and those at highest risk for pneumonitis.
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页数:12
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