Immunotherapy-Mediated Thyroid Dysfunction: Genetic Risk and Impact on Outcomes with PD-1 Blockade in Non-Small Cell Lung Cancer

被引:53
|
作者
Luo, Jia [1 ]
Martucci, Victoria L. [2 ]
Quandt, Zoe [3 ,4 ]
Groha, Stefan [5 ,6 ,7 ]
Murray, Megan H. [8 ]
Lovly, Christine M. [9 ,10 ]
Rizvi, Hira [11 ]
Egger, Jacklynn, V [11 ]
Plodkowski, Andrew J. [12 ]
Abu-Akeel, Mohsen [13 ,14 ]
Schulze, Isabell [13 ,14 ]
Merghoub, Taha [13 ,14 ,15 ]
Cardenas, Eduardo [16 ]
Huntsman, Scott [16 ]
Li, Min [16 ]
Hu, Donglei [16 ]
Gubens, Matthew A. [17 ,18 ]
Gusev, Alexander [5 ,6 ,7 ]
Aldrich, Melinda C. [2 ,10 ]
Hellmann, Matthew D. [1 ,13 ,18 ]
Ziv, Elad [16 ,19 ,20 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, Div Solid Tumor Oncol, Thorac Oncol Serv, New York, NY 10021 USA
[2] Vanderbilt Univ, Med Ctr, Dept Med, Div Genet Med, Nashville, TN USA
[3] Univ Calif San Francisco, Dept Med, Div Diabet Endocrinol & Metab, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Diabet Ctr, San Francisco, CA 94143 USA
[5] Dana Farber Canc Inst, Boston, MA 02115 USA
[6] Harvard Med Sch, Boston, MA 02115 USA
[7] Broad Inst MIT & Harvard, Boston, MA USA
[8] Vanderbilt Univ, Dept Biostat, Sch Med, Nashville, TN USA
[9] Vanderbilt Univ, Med Ctr, Dept Med, Div Hematol & Oncol, Nashville, TN USA
[10] Vanderbilt Univ, Vanderbilt Ingram Canc Ctr, Med Ctr, Nashville, TN USA
[11] Mem Sloan Kettering Canc Ctr, Druckenmiller Ctr Lung Canc Res, 1275 York Ave, New York, NY 10021 USA
[12] Mem Sloan Kettering Canc Ctr, Dept Radiol, 1275 York Ave, New York, NY 10021 USA
[13] Mem Sloan Kettering Canc Ctr, Parker Inst Canc Immunotherapy, 1275 York Ave, New York, NY 10021 USA
[14] Mem Sloan Kettering Canc Ctr, Ludwig Collaborat & Swim Amer Lab, 1275 York Ave, New York, NY 10021 USA
[15] Mem Sloan Kettering Canc Ctr, Dept Med, 1275 York Ave, New York, NY 10021 USA
[16] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[17] Univ Calif San Francisco, Med Oncol, San Francisco, CA 94143 USA
[18] Weill Cornell Med Ctr, Dept Med, New York, NY USA
[19] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, Ctr Genes Environm & Hlth, San Francisco, CA 94143 USA
[20] Univ Calif San Francisco, Inst Human Genet, San Francisco, CA 94143 USA
基金
美国国家卫生研究院;
关键词
GENOME-WIDE ASSOCIATION; ADVERSE EVENTS; IMMUNE; SURVIVAL; PEMBROLIZUMAB; IPILIMUMAB; MICROBIOTA; DISORDERS; LANDSCAPE; NIVOLUMAB;
D O I
10.1158/1078-0432.CCR-21-0921
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Genetic differences in immunity may contribute to toxicity and outcomes with immune checkpoint inhibitor (CPI) therapy, but these relationships are poorly understood. We examined the genetics of thyroid immune- related adverse events (irAE). Experimental Design: In patients with non-small cell lung cancer (NSCLC) treated with CPIs at Memorial Sloan Kettering (MSK) and Vanderbilt University Medical Center (VUMC), we evaluated thyroid irAEs. We typed germline DNA using genome-wide single-nucleotide polymorphism (SNP) arrays and imputed genotypes. Germline SNP imputation was also performed in an independent Dana-Farber Cancer Institute (DFCI) cohort. We developed and validated polygenic risk scores (PRS) for hypothyroidism in noncancer patients using the UK and VUMC BioVU biobanks. These PRSs were applied to thyroid irAEs and CPI response in patients with NSCLC at MSK, VUMC, and DFCI. Results: Among 744 patients at MSK and VUMC, thyroid irAEs occurred in 13% and were associated with improved outcomes [progression-free survival adjusted HR (PFS aHR) = 0.68; 95% confidence interval (CI), 0.52-0.88]. The PRS for hypothyroidism developed from UK Biobank predicted hypothyroidism in the BioVU dataset in noncancer patients [OR per standard deviation (SD) = 1.33, 95% CI, 1.29-1.37; AUROC = 0.6]. The same PRS also predicted development of thyroid irAEs in both independent cohorts of patients treated with CPIs (HR per SD = 1.34; 95% CI, 1.08-1.66; AUROC = 0.6). The results were similar in the DFCI cohort. However, PRS for hypothyroidism did not predict CPI benefit. Conclusions: Thyroid irAEs were associated with response to anti-PD-1 therapy. Genetic risk for hypothyroidism was associated with risk of developing thyroid irAEs. Additional studies are needed to determine whether other irAEs also have shared genetic risk with known autoimmune disorders and the association with treatment response.
引用
收藏
页码:5131 / 5140
页数:10
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