Presentation and outcome of subsequent thyroid cancer among childhood cancer survivors compared to sporadic thyroid cancer: a matched national study.


Journal

European journal of endocrinology
ISSN: 1479-683X
Titre abrégé: Eur J Endocrinol
Pays: England
ID NLM: 9423848

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 24 02 2020
accepted: 20 05 2020
pubmed: 26 5 2020
medline: 2 7 2020
entrez: 26 5 2020
Statut: ppublish

Résumé

Childhood cancer survivors (CCS) are at increased risk to develop differentiated thyroid cancer predominantly after radiotherapy (subsequent DTC). It is insufficiently known whether subsequent DTC in CCS has a different presentation or outcome than sporadic DTC. Patients with subsequent DTC (n = 31) were matched to patients with sporadic DTC (n = 93) on gender, age and year of diagnosis to compare presentation and DTC outcomes. Clinical data were collected retrospectively. Among the CCS with subsequent DTC, all but one had received chemotherapy for their childhood cancer, 19 (61.3%) had received radiotherapy including the thyroid region, 3 (9.7%) 131I-MIBG and 8 (25.8%) had received treatment with chemotherapy only. Subsequent DTC was detected by surveillance through neck palpation (46.2%), as a self-identified mass (34.6%), or by chance. Among sporadic DTC patients, self detection predominated (68.8%). CCS with subsequent DTC tended to have on average smaller tumors (1.9 vs 2.4 cm, respectively, (P = 0.051), and more often bilateral (5/25 (60.0%) vs 28/92 (30.4%), P = 0.024). There were no significant differences in the occurrence of surgical complications, recurrence rate or disease-related death. When compared to patients with sporadic DTC, CCS with subsequent DTC seem to present with smaller tumors and more frequent bilateral tumors. Treatment outcome seems to be similar. The finding that one-third of subsequent DTC cases had been treated with chemotherapy only needs further investigation. These results are important for the development of surveillance programs for CCS at risk for DTC and for treatment guidelines of subsequent DTC.

Identifiants

pubmed: 32449692
doi: 10.1530/EJE-20-0153
pii: EJE-20-0153
doi:
pii:

Substances chimiques

Antineoplastic Agents 0
Iodine Radioisotopes 0
Radiopharmaceuticals 0
3-Iodobenzylguanidine 35MRW7B4AD

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

169-180

Auteurs

Sarah C Clement (SC)

Department of Pediatric Endocrinology, Wilhelmina Children's Hospital/University Medical Center Utrecht, Utrecht, The Netherlands.
Department of Pediatrics, Amsterdam University Medical Center location VU Medical Center, Amsterdam, The Netherlands.

Chantal A Lebbink (CA)

Department of Pediatric Endocrinology, Wilhelmina Children's Hospital/University Medical Center Utrecht, Utrecht, The Netherlands.
Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Mariëlle S Klein Hesselink (MS)

Department of Endocrinology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Jop C Teepen (JC)

Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Thera P Links (TP)

Department of Endocrinology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Cecile M Ronckers (CM)

Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Medical University Brandenburg - Theodor Fontane, Institute of Biostatistics and Registry Research, Neuruppin, Germany.

Hanneke M van Santen (HM)

Department of Pediatric Endocrinology, Wilhelmina Children's Hospital/University Medical Center Utrecht, Utrecht, The Netherlands.
Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

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Classifications MeSH