Thyroid profile during the alternative Sunitinib dosing 2/1 schedule in metastatic renal cell carcinoma.


Journal

Endocrine
ISSN: 1559-0100
Titre abrégé: Endocrine
Pays: United States
ID NLM: 9434444

Informations de publication

Date de publication:
03 2020
Historique:
received: 26 03 2019
accepted: 09 09 2019
pubmed: 5 11 2019
medline: 22 6 2021
entrez: 4 11 2019
Statut: ppublish

Résumé

Hypothyroidism is a common side effect of Sunitinib (SUN) treatment in metastatic renal cell carcinoma (mRCC) patients. We aimed to evaluate thyroid profile during the alternative 2/1 SUN treatment schedule and to assess the predictive value of hypothyroidism in terms of survival. We performed a prospective observational study enrolling 42 consecutive mRCC patients starting first-line alternative SUN dosing 2/1 schedule. Thyroid function was assessed at baseline and during the first three SUN cycles (1 cycle = 6 weeks = 2 ON/1 OFF + 2 ON/1 OFF), and then after 6 and 12 months. Thyroid ultrasound was performed at baseline and after 3, 6, and 12 months. Subclinical hypothyroidism developed in 24% of patients during the first cycle; in other 24% in the second cycle and in 14% in the third cycle. The highest TSH values were reached during the second cycle, ON phase (6.58 ± 5.74 μI U/l). We observed a reduction in thyroid size, in echogenicity and in parenchymal perfusion in all patients. Progression-free survival (PFS) tended to be longer in patients with TSH ≥ 5 μI U/ml during the second cycle (p = 0.069). TSH level was an independent risk factor for PFS in men (p = 0.009) but not in women (p = 0.285). This is the first study investigating functional and morphological effects on thyroid during the alternative 2/1 SUN schedule in mRCC patients. We detected an early onset of subclinical hypothyroidism, observing the association between TSH ≥ 5 μI U/ml and: (i) longer PFS in men; (ii) progressive decrease of thyroid size in absence of significant changes in autoimmune thyroid profile.

Identifiants

pubmed: 31679139
doi: 10.1007/s12020-019-02088-4
pii: 10.1007/s12020-019-02088-4
doi:

Substances chimiques

Antineoplastic Agents 0
Indoles 0
Pyrroles 0
Sunitinib V99T50803M

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

597-604

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Auteurs

L Rizza (L)

Endocrinology Unit, Department of Oncology and Medical Specialities, AO San Camillo-Forlanini, Rome, Italy.

E Sbardella (E)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

D Gianfrilli (D)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

R Lauretta (R)

Internal Medicine, Angiolini Hospital of Bagno di Romagna, Forlì Cesena, Italy.

M Tenuta (M)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

G Del Bene (G)

Department of Radiological, Oncological and Anatomopathological Sciences, Sapienza University of Rome, Rome, Italy.

F Longo (F)

Department of Radiological, Oncological and Anatomopathological Sciences, Sapienza University of Rome, Rome, Italy.

A Faggiano (A)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

A Lenzi (A)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

E Giannetta (E)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy.

C Pozza (C)

Department of Experimental Medicine, Sapienza University of Rome, Rome, Italy. carlotta.pozza@uniroma1.it.

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