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Oncologic progress for the treatment of parathyroid carcinoma is needed.
Christakis, Ioannis; Silva, Angelica M; Kwatampora, Lily Joy; Warneke, Carla L; Clarke, Callisia N; Williams, Michelle D; Grubbs, Elizabeth G; Lee, Jeffrey E; Busaidy, Naifa L; Perrier, Nancy D.
Afiliação
  • Christakis I; Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Silva AM; Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Kwatampora LJ; Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Warneke CL; Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Clarke CN; Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Williams MD; Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Grubbs EG; Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Lee JE; Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Busaidy NL; Department of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Perrier ND; Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas. nperrier@mdanderson.org.
J Surg Oncol ; 114(6): 708-713, 2016 Nov.
Article em En | MEDLINE | ID: mdl-27753088
ABSTRACT
BACKGROUND AND

OBJECTIVES:

Parathyroid carcinoma (PC) is rare but potentially lethal. No standardized staging system or treatment guidelines have been established. We aimed to determine whether management of PC and patient outcomes have changed at our institution over the past 35 years.

METHODS:

Retrospective review of patients with PC at our institution between 1980 and 2015. Patients were grouped by date of initial surgery group 1, 1980-2001; group 2, 2002-2015.

RESULTS:

About 57 patients (26 in group 1; 31 in group 2) were included. Group 2 had more female patients (61%) than group 1 (31%; P = 0.033). Patients in group 2 were older at the time of initial operation (mean age 48 years in group 1 (SD14.3) and 56 years (SD14.6) in group 2; P = 0.034). The 5-year OS rates were 82% (95%CI 59.6%, 93%) for group 1 and 72% (95%CI 45.0%, 87.7%) for group 2. The 5-year DFS rates were 62% (95%CI 36.4%, 79.9%) for group 1 and 66% (95%CI 40.6%, 82.2%) for group 2.

CONCLUSION:

Management of PC and patient outcomes (OS and DFS) have not significantly changed over the past 35 years at our institution. This rare malignancy needs oncologic improvement. J. Surg. Oncol. 2016;114708-713. © 2016 Wiley Periodicals, Inc.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias das Paratireoides / Carcinoma / Paratireoidectomia Tipo de estudo: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Surg Oncol Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias das Paratireoides / Carcinoma / Paratireoidectomia Tipo de estudo: Diagnostic_studies / Guideline / Observational_studies / Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Surg Oncol Ano de publicação: 2016 Tipo de documento: Article