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E-Poster Display

1850P - Immune-related endocrine dysfunction in Chinese: A single tertiary centre experience

Date

17 Sep 2020

Session

E-Poster Display

Topics

Supportive Care and Symptom Management

Tumour Site

Presenters

Wendy Chan

Citation

Annals of Oncology (2020) 31 (suppl_4): S988-S1017. 10.1016/annonc/annonc291

Authors

W.W.L. Chan1, P. Ho2, O. Leung3, K.S. Lau2, J. Au4, V. Lam2, I. Ho4, B. Cheung4, E. Lam2, C. Wong2, R. Liu2, R. Tse2, D. Chow2, T. Tse5, K.O. Lam6, V.H.F. Lee7, H.C.W. Choi7

Author affiliations

  • 1 Department Of Clinical Oncology, The University of Hong Kong, NA - Hong Kong/HK
  • 2 Clinical Oncology, Queen Mary Hospital, Hong Kong/HK
  • 3 Clinical Oncology, The University of Hong Kong, Hong Kong/HK
  • 4 Department Of Clinical Oncology, Queen Mary Hospital, Hong Kong/HK
  • 5 Queen Elizabeth Hospital, Department of Clinical Oncology,, 852 - Kowloon/HK
  • 6 Department Of Clinical Oncology, The University of Hong Kong Li Ka Shing Faculty of Medicine, NA - Pokfulam/HK
  • 7 Department Of Clinical Oncology, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong/HK

Resources

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Abstract 1850P

Background

Cancer immunotherapy, particularly treatment with immune checkpoint inhibitors, has become an important treatment of many cancer types. Use of immune checkpoint inhibitors is often associated with immune-related adverse events (irAEs). Endocrine dysfunction is one of the common irAEs. Majority of the studies on immune-related endocrine dysfunction (irED) were conducted in Western countries and there is few Asian patients data. This study aims to review the frequency and nature of irED in Chinese.

Methods

A retrospective review of all Chinese patients treated for cancer with anti-PD1/ anti-PDL1 or anti-CTLA4 or combination therapy (with chemotherapy or targeted agent) in Department of Clinical Oncology, Queen Mary Hospital, from January 2014 to December 2019 was performed. Demographic data, cancer type and stage, drug treatment, details about irEDs were extracted.

Results

Total 953 patients (male: 603, 64%; median age: 62.0 years) received immune checkpoint inhibitors during the study period. 570 patients (59.8%) used mono-immunotherapy, 133 (14.0%) used dual-immunotherapy, 206 (21.6%) used immunotherapy with chemotherapy and 78 (8.2%) used immunotherapy with targeted agent. 168 patients (17.63%) had hypothyroidism with median onset time 9.9+/-17.5 weeks. 71 patients (11.8%) had hyperthyroidism with median onset time 8.1+/-25.3 weeks. 82 patients (8.6%) had hypocortisolism with median onset time 21.2+/-26.6 weeks. 69 patients (7.2%) had hypercortisolium with median onset time 9.6+/-33.1 weeks. Further analysis on patients developed hypothyroidism was showed in the Table. Table: 1850P

immune-related hypothyroidism

Number of patients with hypothyroidism Percentage Median onset time (week) Standard deviation (week)
mono-immunotherapy 92/570 16.1% 10.1 18.3
dual-immunotherapy 29/133 21.8% 12.4 15.1
Immunotherapy + chemotherapy 29/206 14.1% 12.0 20.8
Immunotherapy + targeted agent 25/78 32.1% 8.4 11.4

Conclusions

Immune checkpoint inhibitors are frequently associated with irEDs with median onset time 8-21 weeks depending on type of irED. Combination of immunotherapy with targeted agents or dual immunotherapy had higher risk of hypothyroidism. Regular endocrine function monitoring should be performed especially in the first six months of treatment.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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