Evaluation of Overall Survival in Patients With Anaplastic Thyroid Carcinoma, 2000-2019.


Journal

JAMA oncology
ISSN: 2374-2445
Titre abrégé: JAMA Oncol
Pays: United States
ID NLM: 101652861

Informations de publication

Date de publication:
01 09 2020
Historique:
pubmed: 8 8 2020
medline: 7 2 2021
entrez: 8 8 2020
Statut: ppublish

Résumé

Anaplastic thyroid carcinoma (ATC) historically has a 4-month median overall survival (OS) from time of diagnosis, with disease-specific mortality approaching 100%. The association between recent major advancements in treatment and OS has yet to be evaluated. To evaluate rates of OS in patients with ATC over the last 2 decades. Retrospective cohort study in a single tertiary care institution. Patients with histopathological confirmation of ATC from January 2000 to October 2019 were included and divided into 3 groups according to date of presentation: 2000-2013, 2014-2016, and 2017-2019. Overall survival compared among different treatment eras and differing therapies, including targeted therapy, immunotherapy, and surgery. Of 479 patients (246 men [51%]; median age, 65.0 [range, 21.1-92.6] years) with ATC evaluated, 52 (11%) were stage IVA, 172 (36%) stage IVB, and 255 (53%) stage IVC at presentation. The median OS of the entire cohort was 0.79 years (9.5 months), ranging from 0.01 to 16.63. The OS at 1 and 2 years was 35% (95% CI, 29%-42%) and 18% (95% CI, 13%-23%) in the 2000-2013 group (n = 227), 47% (95% CI, 36%-56%) and 25% (95% CI, 17%-34%) in the 2014-2016 group (n = 100), and 59% (95% CI, 49%-67%) and 42% (95% CI, 30%-53%) in the 2017-2019 group (n = 152), respectively (P < .001). The hazard ratio was 0.50 (95% CI, 0.38-0.67) for the 2017-2019 group compared with the 2000-2013 patients (P < .001). Factors associated with improved OS included targeted therapy (hazard ratio, 0.49; 95% CI, 0.39-0.63; P < .001), the addition of immunotherapy to targeted therapy (hazard ratio, 0.58; 95% CI, 0.36-0.94; P = .03), and surgery following neoadjuvant BRAF-directed therapy (hazard ratio, 0.29; 95% CI, 0.10-0.78; P = .02). Patients undergoing surgery following neoadjuvant BRAF-directed therapy (n = 20) had a 94% 1-year survival with a median follow-up of 1.21 years. In this large single-institution cohort study spanning nearly 20 years, changes in patient management appear to be associated with significant increase in survival. The era of untreatable ATC is progressively being replaced by molecular-based personalized therapies, with integration of multidisciplinary therapies including surgery and radiation therapy.

Identifiants

pubmed: 32761153
pii: 2769127
doi: 10.1001/jamaoncol.2020.3362
pmc: PMC7411939
doi:

Substances chimiques

Antineoplastic Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1397-1404

Subventions

Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA168505
Pays : United States

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Auteurs

Anastasios Maniakas (A)

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston.

Ramona Dadu (R)

Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston.

Naifa L Busaidy (NL)

Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston.

Jennifer R Wang (JR)

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston.

Renata Ferrarotto (R)

Department of Thoracic Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Charles Lu (C)

Department of Thoracic Head and Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Michelle D Williams (MD)

Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston.

G Brandon Gunn (GB)

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Marie-Claude Hofmann (MC)

Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston.

Gilbert Cote (G)

Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston.

Jared Sperling (J)

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston.

Neil D Gross (ND)

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston.

Erich M Sturgis (EM)

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston.

Ryan P Goepfert (RP)

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston.

Stephen Y Lai (SY)

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston.
Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston.

Maria E Cabanillas (ME)

Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston.

Mark Zafereo (M)

Department of Head and Neck Surgery, The University of Texas MD Anderson Cancer Center, Houston.

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Classifications MeSH