TY - JOUR
T1 - American Association of Clinical Endocrinology Disease State Clinical Review
T2 - Evaluation and Management of Immune Checkpoint Inhibitor-Mediated Endocrinopathies: A Practical Case-Based Clinical Approach
AU - Yuen, Kevin C.J.
AU - Samson, Susan L.
AU - Bancos, Irina
AU - Gosmanov, Aidar R.
AU - Jasim, Sina
AU - Fecher, Leslie A.
AU - Weber, Jeffrey S.
N1 - Funding Information:
Susan L. Samson, MD, PhD, FRCPC, FACE: research grant support from Chiasma
Funding Information:
We thank the American Association of Clinical Endocrinology’s (AACE’s) Clinical Practice Guidelines Oversight Committee for their thoughtful reviews and insightful comments on this manuscript. This clinical review of ICI-mediated endocrinopathies by AACE was developed with financial support from AACE. All members who served on this AACE Task Force completed work on the manuscript electronically and met via video conferences.
Funding Information:
We thank the American Association of Clinical Endocrinology's (AACE's) Clinical Practice Guidelines Oversight Committee for their thoughtful reviews and insightful comments on this manuscript. This clinical review of ICI-mediated endocrinopathies by AACE was developed with financial support from AACE. All members who served on this AACE Task Force completed work on the manuscript electronically and met via video conferences. The Task Force was empaneled in accordance with American Association of Clinical Endocrinology's (AACE's) Conflict of Interest (COI) Policy and approved by the AACE COI Subcommittee. All members of the expert Task Force completed the AACE's disclosure form regarding any multiplicities of interests related to commercial and direct financial relationships within the preceding 12 months with companies that develop products connected with endocrine disorders. The categories for disclosure include employment, stock or other ownership, direct financial relationships (eg. speaker or consultant), research funding, authorship or panel involvement on a guideline related to an overlapping topic, or other situations related to a perceived COI. The AACE COI Subcommittee reviewed these disclosures against an AACE-approved list of affected companies for this clinical review and reached a consensus regarding members who could serve on the Task Force in the nonconflicted majority, those who could serve in the conflicted minority with management strategy, and those who were disqualified from serving on the Task Force. The AACE Clinical Practice Guidelines Oversight Committee reviewed and approved the AACE COI Subcommittee's decisions regarding manageable COI and empanelment. The members of this Task Force were reminded to update potential disclosures if new potential conflicts arose during their appointments and to verify the currency of the disclosures. AACE made every effort to minimize the potential for COI that could influence the information presented in this clinical review. Co-Chairs of the Task Force, Kevin C. J. Yuen, MD, FRCP, FACE: research grant support to Barrow Neurological Institute from Ascendis, Corcept, and Amryt and has served as an advisory board member for Novo Nordisk, Ascendis, Corcept, Ipsen, Chiasma, Strongbridge, Crinetics, and Recordati, Susan L. Samson, MD, PhD, FRCPC, FACE: research grant support from Chiasma, Task Force Members, Irina Bancos, MD: consultant for Sparrow Pharmaceutics, advisory board member for HRA Pharma, past advisory board member for Strongbridge, safety board member for Adrenas ALL, Aidar R. Gosmanov, MD, PhD, FACE: consultant or speaker's bureau on diabetes for AstraZeneca; research support from AbbVie and KOWA Research Institute, Sina Jasim, MD, MPH: reports no potential conflicts of interest, Leslie Fecher, MD, American Society of Clinical Oncology (ASCO) Representative: consultant for ViaOncology/Elsevier; research grant support from BMS, EMD, Serono, Pfizer, Array, and Kartos, Jeffrey S. Weber, MD, PhD, ASCO Representative: stock ownership in Biond, Evaxion, Instil Bio, OncoC4, and Neximmune; consultant for Merck, Genentech, Astra Zeneca, GSK, Novartis, Nektar, Celldex, Incyte, Biond, ImCheck, Sellas, Evaxion, and EMD Serono; advisory board for BMS; scientific advisory boards for Instil Bio, Evaxion, ImCheck, Biond, OncoC4, Sellas, and Neximmune; research grant support from BMS, Merck, GSK, Moderna, Pfizer, Novartis, and Astra Zeneca, Panel Composition, The Task Force was empaneled in accordance with the AACE's COI Policy and the Diversity, Equity, and Inclusion Policy. This evidence-based clinical practice guideline was developed by a multidisciplinary group of credentialed medical professionals from the fields of endocrinology and oncology. The members of the Task Force included current AACE members in good standing and 2 ASCO representatives. Review Process, The drafts of this manuscript were reviewed and approved by the writing Task Force, AACE CPG Oversight Committee, AACE Board of Directors, and peer reviewers for Endocrine Practice.
Funding Information:
Leslie Fecher, MD, American Society of Clinical Oncology (ASCO) Representative: consultant for ViaOncology/Elsevier; research grant support from BMS, EMD, Serono, Pfizer, Array, and Kartos
Publisher Copyright:
© 2022 AACE
PY - 2022/7
Y1 - 2022/7
N2 - Objective: The aim of this case-based clinical review was to provide a practical approach for clinicians regarding the management of patients with immune checkpoint inhibitor (ICI)-mediated endocrinopathies. Methods: A literature search of PubMed, Embase, and Scopus was conducted using appropriate keywords. The discussions and strategies for the diagnosis and management of ICI-mediated endocrinopathies are based on evidence available from prospective, randomized clinical studies; cohort studies; cross-sectional studies; case-based studies; and an expert consensus. Results: Immunotherapy with ICIs has transformed the treatment landscape of diverse types of cancers but frequently results in immune-mediated endocrinopathies that can cause acute and persistent morbidity and, rarely, death. The patterns of endocrinopathies differ between the inhibitors of the cytotoxic T-lymphocyte antigen 4 and programmed cell death protein 1 or programmed cell death protein 1 ligand pathways but most often involve the thyroid and pituitary glands. The less common but important presentations include insulin-deficient diabetes mellitus, primary adrenal insufficiency, primary hypoparathyroidism, central diabetes insipidus, primary hypogonadism, and pancreatitis, with or without subsequent progression to diabetes mellitus or exocrine insufficiency. Conclusion: In recent years, with increasing numbers of patients with cancer being treated with ICIs, more clinicians in a variety of specialties have been called upon to diagnose and treat ICI-mediated endocrinopathies. Herein, we reviewed case scenarios of various clinical manifestations and emphasized the need for a high index of clinical suspicion by all clinicians caring for these patients, including endocrinologists, oncologists, primary care providers, and emergency department physicians. We also provided diagnostic and therapeutic approaches for ICI-induced endocrinopathies and proposed that patients on ICI therapy be evaluated and treated by a multidisciplinary team in collaboration with endocrinologists.
AB - Objective: The aim of this case-based clinical review was to provide a practical approach for clinicians regarding the management of patients with immune checkpoint inhibitor (ICI)-mediated endocrinopathies. Methods: A literature search of PubMed, Embase, and Scopus was conducted using appropriate keywords. The discussions and strategies for the diagnosis and management of ICI-mediated endocrinopathies are based on evidence available from prospective, randomized clinical studies; cohort studies; cross-sectional studies; case-based studies; and an expert consensus. Results: Immunotherapy with ICIs has transformed the treatment landscape of diverse types of cancers but frequently results in immune-mediated endocrinopathies that can cause acute and persistent morbidity and, rarely, death. The patterns of endocrinopathies differ between the inhibitors of the cytotoxic T-lymphocyte antigen 4 and programmed cell death protein 1 or programmed cell death protein 1 ligand pathways but most often involve the thyroid and pituitary glands. The less common but important presentations include insulin-deficient diabetes mellitus, primary adrenal insufficiency, primary hypoparathyroidism, central diabetes insipidus, primary hypogonadism, and pancreatitis, with or without subsequent progression to diabetes mellitus or exocrine insufficiency. Conclusion: In recent years, with increasing numbers of patients with cancer being treated with ICIs, more clinicians in a variety of specialties have been called upon to diagnose and treat ICI-mediated endocrinopathies. Herein, we reviewed case scenarios of various clinical manifestations and emphasized the need for a high index of clinical suspicion by all clinicians caring for these patients, including endocrinologists, oncologists, primary care providers, and emergency department physicians. We also provided diagnostic and therapeutic approaches for ICI-induced endocrinopathies and proposed that patients on ICI therapy be evaluated and treated by a multidisciplinary team in collaboration with endocrinologists.
KW - adrenalitis
KW - diabetes mellitus
KW - endocrinopathy
KW - hypophysitis
KW - immune checkpoint inhibitor
KW - thyroiditis
UR - http://www.scopus.com/inward/record.url?scp=85132756246&partnerID=8YFLogxK
U2 - 10.1016/j.eprac.2022.04.010
DO - 10.1016/j.eprac.2022.04.010
M3 - Review article
C2 - 35477029
AN - SCOPUS:85132756246
SN - 1530-891X
VL - 28
SP - 719
EP - 731
JO - Endocrine Practice
JF - Endocrine Practice
IS - 7
ER -