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Immunotherapy-Mediated Thyroid Dysfunction: Genetic Risk and Impact on Outcomes with PD-1 Blockade in Non-Small Cell Lung Cancer.
Luo, Jia; Martucci, Victoria L; Quandt, Zoe; Groha, Stefan; Murray, Megan H; Lovly, Christine M; Rizvi, Hira; Egger, Jacklynn V; Plodkowski, Andrew J; Abu-Akeel, Mohsen; Schulze, Isabell; Merghoub, Taha; Cardenas, Eduardo; Huntsman, Scott; Li, Min; Hu, Donglei; Gubens, Matthew A; Gusev, Alexander; Aldrich, Melinda C; Hellmann, Matthew D; Ziv, Elad.
Afiliação
  • Luo J; Thoracic Oncology Service, Division of Solid Tumor Oncology, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Martucci VL; Department of Medicine, Division of Genetic Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Quandt Z; Division of Diabetes, Endocrinology and Metabolism, Department of Medicine, University of California, San Francisco, California.
  • Groha S; Diabetes Center, University of California, San Francisco, California.
  • Murray MH; Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Lovly CM; Harvard Medical School, Boston, Massachusetts.
  • Rizvi H; Broad Institute of MIT and Harvard, Boston, Massachusetts.
  • Egger JV; Department of Biostatistics, Vanderbilt University School of Medicine, Nashville, Tennessee.
  • Plodkowski AJ; Department of Medicine, Division of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Abu-Akeel M; Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, Tennessee.
  • Schulze I; Druckenmiller Center for Lung Cancer Research, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Merghoub T; Druckenmiller Center for Lung Cancer Research, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Cardenas E; Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Huntsman S; Parker Institute for Cancer Immunotherapy at Memorial Sloan Kettering Cancer Center, New York, New York.
  • Li M; Ludwig Collaborative and Swim Across America Laboratory, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Hu D; Parker Institute for Cancer Immunotherapy at Memorial Sloan Kettering Cancer Center, New York, New York.
  • Gubens MA; Ludwig Collaborative and Swim Across America Laboratory, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Gusev A; Parker Institute for Cancer Immunotherapy at Memorial Sloan Kettering Cancer Center, New York, New York.
  • Aldrich MC; Ludwig Collaborative and Swim Across America Laboratory, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Hellmann MD; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Ziv E; Department of Medicine, University of California San Francisco, San Francisco, California.
Clin Cancer Res ; 27(18): 5131-5140, 2021 09 15.
Article em En | MEDLINE | ID: mdl-34244291
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Doenças da Glândula Tireoide / Carcinoma Pulmonar de Células não Pequenas / Inibidores de Checkpoint Imunológico / Imunoterapia / Neoplasias Pulmonares Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Cancer Res Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Doenças da Glândula Tireoide / Carcinoma Pulmonar de Células não Pequenas / Inibidores de Checkpoint Imunológico / Imunoterapia / Neoplasias Pulmonares Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Cancer Res Ano de publicação: 2021 Tipo de documento: Article