» Articles » PMID: 31807385

Incidence and Risk of Thyroid Dysfunction in Advanced or Metastatic Non-small Cell Lung Cancer Patients Treated with Pembrolizumab: A Meta-analysis

Overview
Journal Cureus
Date 2019 Dec 7
PMID 31807385
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Thyroid dysfunction is one of the major side effects associated with Pembrolizumab in the treatment of advanced or metastatic non-small cell lung cancer (NSCLC). We performed a systematic review and meta-analysis of randomized clinical trials to determine its overall incidence. A literature search was conducted using the electronic database engines PubMed and Google Scholar from inception to March 2019. Eligible studies were prospective randomized clinical trials with advanced or metastatic NSCLC. The pooled incidence, risk ratio (RR), and 95% confidence interval (CI) of thyroid dysfunction were calculated using the random-effect model. Given the possibility of a between-study variance, we used the random-effect model rather than the fixed-effect model. A total of four studies, including 1603 patients, were selected for analysis. Among patients receiving Pembrolizumab, the overall incidence of all-grade thyroid dysfunction was 19.8% (95% CI: 16.6-23.3%). Pembrolizumab was associated with a significantly increased risk of thyroid dysfunction of all grades, with a relative risk of 3.9 (95% CI: 2.08-7.42%, p= 0.084) in comparison with the controls. Therefore, there is a significant increase in developing thyroid dysfunction in advanced or metastatic NSCLC patients treated with Pembrolizumab.

Citing Articles

CAR-engineered NK cells versus CAR T cells in treatment of glioblastoma; strength and flaws.

Sabahi M, Fathi Jouzdani A, Sadeghian Z, Dabbagh Ohadi M, Sultan H, Salehipour A J Neurooncol. 2024; 171(3):495-530.

PMID: 39538038 DOI: 10.1007/s11060-024-04876-z.


Immune-Related Thyroiditis in Patients with Advanced Lung Cancer Treated with Immune Checkpoint Inhibitors: Imaging Features and Clinical Implications.

Park H, Hata A, Hatabu H, Ricciuti B, Awad M, Nishino M Cancers (Basel). 2023; 15(3).

PMID: 36765606 PMC: 9913779. DOI: 10.3390/cancers15030649.


Assessment of TMB, PD-L1, and lymphocyte to monocyte ratio as predictive potential in a phase Ib study of sintilimab in patients with advanced solid tumors.

Jiang H, Li N, Wang H, Chen Z, Zheng Y, Qian J Am J Cancer Res. 2021; 11(9):4259-4276.

PMID: 34659886 PMC: 8493392.


Thyroid Dysfunction in Lung Cancer Patients Treated with Immune Checkpoint Inhibitors (ICIs): Outcomes in a Multiethnic Urban Cohort.

DAiello A, Lin J, Gucalp R, Tabatabaie V, Cheng H, Bloomgarden N Cancers (Basel). 2021; 13(6).

PMID: 33806774 PMC: 8004603. DOI: 10.3390/cancers13061464.

References
1.
Dong H, Chen L . B7-H1 pathway and its role in the evasion of tumor immunity. J Mol Med (Berl). 2003; 81(5):281-7. DOI: 10.1007/s00109-003-0430-2. View

2.
Brahmer J, Lacchetti C, Thompson J . Management of Immune-Related Adverse Events in Patients Treated With Immune Checkpoint Inhibitor Therapy: American Society of Clinical Oncology Clinical Practice Guideline Summary. J Oncol Pract. 2018; 14(4):247-249. DOI: 10.1200/JOP.18.00005. View

3.
Keir M, Butte M, Freeman G, Sharpe A . PD-1 and its ligands in tolerance and immunity. Annu Rev Immunol. 2008; 26:677-704. PMC: 10637733. DOI: 10.1146/annurev.immunol.26.021607.090331. View

4.
Gong J, Chehrazi-Raffle A, Reddi S, Salgia R . Development of PD-1 and PD-L1 inhibitors as a form of cancer immunotherapy: a comprehensive review of registration trials and future considerations. J Immunother Cancer. 2018; 6(1):8. PMC: 5778665. DOI: 10.1186/s40425-018-0316-z. View

5.
Lee H, Hodi F, Giobbie-Hurder A, Ott P, Buchbinder E, Haq R . Characterization of Thyroid Disorders in Patients Receiving Immune Checkpoint Inhibition Therapy. Cancer Immunol Res. 2017; 5(12):1133-1140. PMC: 5748517. DOI: 10.1158/2326-6066.CIR-17-0208. View