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Article: Immune-Related Endocrine Dysfunctions in Combined Modalities of Treatment: Real-World Data

TitleImmune-Related Endocrine Dysfunctions in Combined Modalities of Treatment: Real-World Data
Authors
Keywordsimmune checkpoint inhibitors
immune-related endocrine dysfunction
hypothyroidism
targeted therapy
malignancy
Issue Date2021
PublisherMDPI AG. The Journal's web site is located at http://www.mdpi.com/journal/cancers/
Citation
Cancers, 2021, v. 13 n. 15, p. article no. 3797 How to Cite?
AbstractThe number of immune-related endocrine dysfunctions (irEDs) has concurrently increased with the widespread use of immunotherapy in clinical practice and further expansion of the approved indications for immune checkpoint inhibitor (ICI) in cancer management. A retrospective analysis was conducted on consecutive patients ≥18 years of age with advanced solid malignancies who had received at least one dose of anti-programmed cell death protein 1 (anti-PD-1) and/or anti-CTLA4 antibodies between January 2014 and December 2019 at a university hospital in Hong Kong. Patients were reviewed up to two months after the last administration of an ICI. The types, onset times and grades of irEDs, including hypothyroidism, hyperthyroidism, adrenal insufficiency and immune-related diabetes mellitus, were recorded. Factors associated with irEDs were identified using multivariate analysis. A total of 953 patients (male: 603, 64.0%; median age: 62.0 years) were included. Of these, 580 patients (60.9%) used ICI-alone, 132 (13.9%) used dual-ICI, 187 (19.6%) used an ICI combined with chemotherapy (chemo + ICI), and 54 (5.70%) used immunotherapy with a targeted agent (targeted + ICI). A significantly higher proportion of patients using targeted + ICI had irEDs and hypothyroidism; in contrast, a higher proportion of patients using dual-ICI had adrenal insufficiency. There was no significant difference in the incidence of irED between the younger (<65 years) and older (≥65 years) patients. Using logistic regression, only treatment type was significantly associated with irEDs. Notably, older patients had a higher risk of having immune-related diabetes mellitus. This large, real-world cohort demonstrates that targeted + ICI has a higher risk of overall irED and hypothyroidism. Immunotherapy is safe and well-tolerated regardless of age, but close monitoring of fasting glucose is essential in older populations.
Persistent Identifierhttp://hdl.handle.net/10722/302113
ISSN
2023 Impact Factor: 4.5
2023 SCImago Journal Rankings: 1.391
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChan, WLW-
dc.contributor.authorChoi, CW-
dc.contributor.authorHo, PYP-
dc.contributor.authorLau, KS-
dc.contributor.authorTse, PY-
dc.contributor.authorAu, J-
dc.contributor.authorLam, V-
dc.contributor.authorLiu, R-
dc.contributor.authorH人, I-
dc.contributor.authorWong, C-
dc.contributor.authorCheung, B-
dc.contributor.authorLam, E-
dc.contributor.authorChow, D-
dc.contributor.authorLam, KO-
dc.contributor.authorYuen, KK-
dc.contributor.authorKwong, DLW-
dc.date.accessioned2021-08-21T03:31:46Z-
dc.date.available2021-08-21T03:31:46Z-
dc.date.issued2021-
dc.identifier.citationCancers, 2021, v. 13 n. 15, p. article no. 3797-
dc.identifier.issn2072-6694-
dc.identifier.urihttp://hdl.handle.net/10722/302113-
dc.description.abstractThe number of immune-related endocrine dysfunctions (irEDs) has concurrently increased with the widespread use of immunotherapy in clinical practice and further expansion of the approved indications for immune checkpoint inhibitor (ICI) in cancer management. A retrospective analysis was conducted on consecutive patients ≥18 years of age with advanced solid malignancies who had received at least one dose of anti-programmed cell death protein 1 (anti-PD-1) and/or anti-CTLA4 antibodies between January 2014 and December 2019 at a university hospital in Hong Kong. Patients were reviewed up to two months after the last administration of an ICI. The types, onset times and grades of irEDs, including hypothyroidism, hyperthyroidism, adrenal insufficiency and immune-related diabetes mellitus, were recorded. Factors associated with irEDs were identified using multivariate analysis. A total of 953 patients (male: 603, 64.0%; median age: 62.0 years) were included. Of these, 580 patients (60.9%) used ICI-alone, 132 (13.9%) used dual-ICI, 187 (19.6%) used an ICI combined with chemotherapy (chemo + ICI), and 54 (5.70%) used immunotherapy with a targeted agent (targeted + ICI). A significantly higher proportion of patients using targeted + ICI had irEDs and hypothyroidism; in contrast, a higher proportion of patients using dual-ICI had adrenal insufficiency. There was no significant difference in the incidence of irED between the younger (<65 years) and older (≥65 years) patients. Using logistic regression, only treatment type was significantly associated with irEDs. Notably, older patients had a higher risk of having immune-related diabetes mellitus. This large, real-world cohort demonstrates that targeted + ICI has a higher risk of overall irED and hypothyroidism. Immunotherapy is safe and well-tolerated regardless of age, but close monitoring of fasting glucose is essential in older populations.-
dc.languageeng-
dc.publisherMDPI AG. The Journal's web site is located at http://www.mdpi.com/journal/cancers/-
dc.relation.ispartofCancers-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectimmune checkpoint inhibitors-
dc.subjectimmune-related endocrine dysfunction-
dc.subjecthypothyroidism-
dc.subjecttargeted therapy-
dc.subjectmalignancy-
dc.titleImmune-Related Endocrine Dysfunctions in Combined Modalities of Treatment: Real-World Data-
dc.typeArticle-
dc.identifier.emailChan, WLW: winglok@hku.hk-
dc.identifier.emailChoi, CW: hcchoi@hku.hk-
dc.identifier.emailHo, PYP: pattyho@hku.hk-
dc.identifier.emailLam, KO: lamkaon@hku.hk-
dc.identifier.emailKwong, DLW: dlwkwong@hku.hk-
dc.identifier.authorityChan, WLW=rp02541-
dc.identifier.authorityChoi, CW=rp02815-
dc.identifier.authorityLam, KO=rp01501-
dc.identifier.authorityKwong, DLW=rp00414-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.3390/cancers13153797-
dc.identifier.pmid34359698-
dc.identifier.pmcidPMC8345182-
dc.identifier.scopuseid_2-s2.0-85111270126-
dc.identifier.hkuros324282-
dc.identifier.volume13-
dc.identifier.issue15-
dc.identifier.spagearticle no. 3797-
dc.identifier.epagearticle no. 3797-
dc.identifier.isiWOS:000681861500001-
dc.publisher.placeSwitzerland-

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