ECE2021 Oral Communications Oral Communications 10: Thyroid (6 abstracts)
1Città della Salute e della Scienza Hospital, Transition Unit for Childhood Cancer Survivors, Turin, Italy; 2Città della Salute e della Scienza Hospital, Division of Endocrinology, Diabetology, and Metabolism, Turin, Italy; 3Città della Salute e della Scienza Hospital, Department of Medical Sciences, University of Turin, Turin, Italy; 4Città della Salute e della Scienza Hospital, Department of Oncology, Stem Cell Transplant Center, Turin, Italy; 5Città della Salute e della Scienza Hospital, Department of Molecular Biotechnology and Health Sciences, University of Turin, Turin, Italy; 6Città della Salute e della Scienza Hospital, Division of Oncological Endocrinology, Turin, Italy; 7Perlmutter Cancer Center, Division of Hematology and Medical Oncology, NYU School of Medicine, New York, United States
Introduction
Primary hypothyroidism, which is one of the main endocrine complications of allogenic stem cells transplantation (allo-SCT), has been largely studied in children. Conversely, data on adults are still limited with a reported incidence widely ranging between 9 and 47%. Older age, multiple allo-SCT, chronic Graft vs Host Disease (cGVHD), prolonged immunosuppressive therapy and high-dose total body irradiation (TBI) have been indicated as potential risk factors. The aims of this observational, cross-sectional study were to assess the prevalence of post-allo-SCT hypothyroidism in adult recipients, to analyse its variation over time and to detect predictive factors.
Methods
Among 462 patients who underwent allo-SCT at our hospital between January 2010 and December 2017, 218 where alive and in active follow-up at the time of the study. Of them, 195 (M 107; F 88; median age 53.3 years) were recruited and divided into 3 groups according to time elapsed after allo-SCT (1–3 years: n 78; 3–5 years: n 50; >5 years: n 67). Data on pre-transplant TSH and fTc levels were available for all patients. After the transplant, TSH, fT4 and anti-thyroperoxidase antibodies (AbTPO) were evaluated.
Results
TSH levels were significantly lower before (median 1.7, IQR 1.2–2.4 µU/ml) than after allo-SCT (median 2.3, IQR 1.5–3.5 µU/ml; P < 0.0001). Forty-six (23.6%) patients developed post-transplant hypothyroidism, with a higher prevalence in females (F 35.2%, M 14.0%; P < 0.001) and at earlier time points (1–3 yrs: 28.2%; 3–5 yrs: 24%; >5 yrs: 17.9%). At the pre-transplant evaluation, patients who developed hypothyroidism showed higher TSH and lower fT4 levels (TSH median 2.4, IQR 1.7–3.3 µU/ml; fT4 median 10.2, IQR 8.9–11.7 pg/ml) compared to those with preserved thyroid function (TSH median 1.5, IQR 1.1–2.1 µU/ml; fT4 median 11.2, IQR 10.0–12.1 pg/ml; P < 0.0001 and < 0.05, respectively). Patients with post-transplant hypothyroidism had higher prevalence of AbTPO positivity and of acute GvHD (P < 0.05 for both). Multiple regression analysis, corrected for time after allo-SCT, radiotherapy and acute GVHD, identified male gender as a negative predictor of hypothyroidism (OR 0.283, 95%IC 0.121–0.660; P < 0.05) and higher pre-transplant TSH levels as a positive one (OR 1.797, 95%IC 1.275–2.534; P < 0.001).
Conclusions
About one out of four patients developed hypothyroidism after allo-SCT, with a greater risk for females and in the presence of acute GHVD. Pre-transplant TSH levels seem to predict the onset of post-SCT hypothyroidism.