Baseline serum TSH levels predict the absence of thyroid dysfunction in cancer patients treated with immunotherapy.
Baseline serum TSH levels predict the absence of thyroid dysfunction in cancer patients treated with immunotherapy.
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DOI:
10.1007/s40618-020-01480-6
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发表时间:
2021-08
影响因子:
5.4
通讯作者:
Castagna MG
中科院分区:
文献类型:
--
作者:
Brilli L;Danielli R;Campanile M;Secchi C;Ciuoli C;Calabrò L;Pilli T;Cartocci A;Pacini F;Di Giacomo AM;Castagna MG
Immunotherapy against immune checkpoints has significantly improved survival both in metastatic and adjuvant setting in several types of cancers. Thyroid dysfunction is the most common endocrine adverse event reported. Patients who are at risk of developing thyroid dysfunction remain to be defined. We aimed to identify predictive factors for the development of thyroid dysfunction during immunotherapy. This is a retrospective study including a total of 68 patients who were treated with immune checkpoint inhibitors (ICIs) for metastatic or unresectable advanced cancers. The majority of patients were treated with anti-PD1 drugs in monotherapy or in combination with anti-CTLA4 inhibitors. Thyroid function and anti-thyroid antibodies, before starting immunotherapy and during treatment, were evaluated. Thyroid ultrasound was also performed in a subgroup of patients at the time of enrolment in the study. Eleven out of 68 patients (16.1%) developed immune-related overt thyroid dysfunction. By ROC curve analysis, we found that a serum TSH cut-off of 1.72 mUI/l, at baseline, had a good diagnostic accuracy in identifying patients without overt thyroid dysfunction (NPV = 100%, p = 0.0029). At multivariate analysis, both TSH and positive anti-thyroid antibodies (ATAbs) levels, before ICIs treatment, were independently associated with the development of overt thyroid dysfunction during immunotherapy (p = 0.0001 and p = 0.009, respectively). Pre-treatment serum TSH and ATAbs levels may help to identify patients at high risk for primary thyroid dysfunction. Our study suggests guidance for an appropriate timely screening and for a tailored management of thyroid dysfunctions in patients treated with ICIs.
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影响因子:
6.6
作者:
Basak, Edwin A.;van der Meer, Jan W. M.;Medici, Marco
通讯作者:
Medici, Marco
影响因子:
5.7
作者:
Kimbara S;Fujiwara Y;Iwama S;Ohashi K;Kuchiba A;Arima H;Yamazaki N;Kitano S;Yamamoto N;Ohe Y
通讯作者:
Ohe Y
影响因子:
2.9
作者:
Olsson-Brown, Anna;Lord, Rosemary;Pirmohamed, Munir
通讯作者:
Pirmohamed, Munir
DOI:
10.1210/jc.2016-2300
发表时间:
2016-11
期刊:
The Journal of clinical endocrinology and metabolism
影响因子:
--
作者:
de Filette J;Jansen Y;Schreuer M;Everaert H;Velkeniers B;Neyns B;Bravenboer B
通讯作者:
Bravenboer B
影响因子:
4.4
作者:
Girotra M;Hansen A;Farooki A;Byun DJ;Min L;Creelan BC;Callahan MK;Atkins MB;Sharon E;Antonia SJ;West P;Gravell AE;Investigational Drug Steering Committee (IDSC) Immunotherapy Task Force collaboration
通讯作者:
Investigational Drug Steering Committee (IDSC) Immunotherapy Task Force collaboration