Recombinant Thyrotropin vs Levothyroxine Withdrawal in 131I Therapy of N1 Thyroid Cancer: A Large Matched Cohort Study (ThyrNod).


Journal

The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362

Informations de publication

Date de publication:
01 04 2019
Historique:
received: 23 07 2018
accepted: 31 10 2018
pubmed: 7 11 2018
medline: 15 2 2020
entrez: 7 11 2018
Statut: ppublish

Résumé

Recombinant human thyrotropin (rhTSH) has been shown to be an effective stimulation method for radioactive iodine (RAI) therapy in differentiated thyroid cancer, including in those with nodal metastases (N1 DTC). To demonstrate the noninferiority of rhTSH vs thyroid hormone withdrawal (THW) in preparation to RAI regarding disease status at the first evaluation in the real-life setting in patients with N1 DTC. This was a French multicenter retrospective study. Groups were matched according to age (<45/≥45 years), number of N1 nodes (≤5/>5 lymph nodes), and stage (pT1-T2/pT3). The cohort consisted of 404 patients pT1-T3/N1/M0 DTC treated with rhTSH (n = 205) or THW (n = 199). Pathological characteristics and initially administrated RAI activities (3.27 ± 1.00 GBq) were similar between the two groups. At first evaluation (6 to 18 months post-RAI), disease-free status was defined by thyroglobulin levels below threshold and a normal ultrasound. Disease-free rate was not inferior in the rhTSH group (75.1%) compared with the THW group (71.9%). The observed difference between the success rates was 3.3% (-6.6 to 13.0); rhTSH was therefore considered noninferior to THW because the upper limit of this interval was <15%. At the last evaluation (29.7 ± 20.7 months for rhTSH; 36.7 ± 23.8 months for THW), 83.5% (rhTSH) and 81.5% (THW) of patients achieved a complete response. This result was not influenced by any of the known prognostic factors. A preparation for initial RAI treatment with rhTSH was noninferior to that with THW in our series of pT1-T3/N1/M0-DTC on disease-free status outcomes at the first evaluation and after 3 years.

Identifiants

pubmed: 30398518
pii: 5155461
doi: 10.1210/jc.2018-01589
doi:

Substances chimiques

Iodine Radioisotopes 0
Iodine-131 0
Recombinant Proteins 0
Thyrotropin 9002-71-5
Thyroxine Q51BO43MG4

Types de publication

Comparative Study Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1020-1028

Informations de copyright

Copyright © 2019 Endocrine Society.

Auteurs

Laurence Leenhardt (L)

Pitié-Salpêtrière Hospital, Sorbonne Université, Paris, France.

Sophie Leboulleux (S)

Gustave Roussy, Univ. Paris Saclay, Villejuif, France.

Claire Bournaud (C)

Hospices Civils de Lyon, Lyon, France.

Slimane Zerdoud (S)

Institute University du Cancer, Toulouse, France.

Claire Schvartz (C)

Jean Godinot Centre, Reims, France.

Renaud Ciappuccini (R)

François Baclesse Centre, Caen, France.

Antony Kelly (A)

Jean Perrin Centre, Clermont-Ferrand, France.

Olivier Morel (O)

Paul Papin Centre, Angers, France.

Inna Dygai-Cochet (I)

Georges François Leclerc Centre, Dijon, France.

Daniela Rusu (D)

René Gauducheau Centre, Saint Herblain Cedex, France.

Cécile N Chougnet (CN)

Saint-Louis Hospital, Paris, France.

Georges Lion (G)

Centre Hospitalier Régional Universitaire de Lille, Lille, France.

Marie-Claude Eberlé-Pouzeratte (MC)

Montpellier Cancer Institute, Montpellier, France.

Bogdan Catargi (B)

Institute University du Cancer, Toulouse, France.

Marmar Kabir-Ahmadi (M)

St André Hospital, Bordeaux, France.

Eliane Le Peillet Feuillet (E)

Sanofi Genzyme, Saint Germain en Laye Cedex, France.

David Taïeb (D)

Aix-Marseille University, La Timone University Hospital, European Center for Research in Medical Imaging, Marseille, France.

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Classifications MeSH