Clinical Presentation, Treatment, and Outcome of Parathyroid Carcinoma: Results of the NEKAR Retrospective International Multicenter Study.


Journal

Annals of surgery
ISSN: 1528-1140
Titre abrégé: Ann Surg
Pays: United States
ID NLM: 0372354

Informations de publication

Date de publication:
01 02 2022
Historique:
pubmed: 11 7 2020
medline: 19 2 2022
entrez: 11 7 2020
Statut: ppublish

Résumé

In this retrospective cohort study, we describe the clinical presentation and workup of parathyroid carcinoma (PC) and determine its clinical prognostic parameters. Primary outcome was recurrence free survival. PC is an orphan malignancy for which diagnostic workup and treatment is not established. Eighty-three patients were diagnosed with PC between 1986 and 2018. Disease-specific and recurrence-free survivals were estimated with the Kaplan-Meier method. Risk factors for recurrence were identified by binary logistic regression with adjustment for age and sex. Thirty-nine tumors underwent central histopathological review. Renal (39.8%), gastrointestinal (24.1%), bone (22.9%), and psychiatric (19.3%) symptoms were the most common symptoms. Surgical treatment was heterogeneous [parathyroidectomy [PTx)] alone: 22.9%; PTx and hemithyroidectomy: 24.1%; en bloc resection 15.7%; others 37.3%] and complications of surgery were frequent (recurrent laryngeal nerve palsy 25.3%; hypoparathyroidism 6%). Recurrence of PC was observed in 32 of 83 cases. In univariate analysis, rate of recurrence was reduced when extended initial surgery had been performed (P = 0.04). In multivariate analysis low T status [odds ratio (OR) = 2.65, 95% confidence interval (CI) 1.02-6.88, P = 0.045], N0 stage at initial diagnosis (OR = 6.32, 95% CI 1.33-30.01, P = 0.02), Ki-67 <10% (OR = 14.07, 95% CI 2.09-94.9, P = 0.007), and postoperative biochemical remission (OR = 0.023, 95% CI 0.001-0.52, P = 0.018) were beneficial prognostic parameters for recurrence-free survival. Despite a favorable overall prognosis, PC shows high rates of recurrence leading to repeated surgery and postoperative recurrent laryngeal nerve palsy and hypoparathyroidism. In view of the reduced recurrence rate in cases of extended surgery, ipsilateral completion surgery may be considered when PC is confirmed.

Sections du résumé

OBJECTIVE
In this retrospective cohort study, we describe the clinical presentation and workup of parathyroid carcinoma (PC) and determine its clinical prognostic parameters. Primary outcome was recurrence free survival.
SUMMARY BACKGROUND DATA
PC is an orphan malignancy for which diagnostic workup and treatment is not established.
METHODS
Eighty-three patients were diagnosed with PC between 1986 and 2018. Disease-specific and recurrence-free survivals were estimated with the Kaplan-Meier method. Risk factors for recurrence were identified by binary logistic regression with adjustment for age and sex. Thirty-nine tumors underwent central histopathological review.
RESULTS
Renal (39.8%), gastrointestinal (24.1%), bone (22.9%), and psychiatric (19.3%) symptoms were the most common symptoms. Surgical treatment was heterogeneous [parathyroidectomy [PTx)] alone: 22.9%; PTx and hemithyroidectomy: 24.1%; en bloc resection 15.7%; others 37.3%] and complications of surgery were frequent (recurrent laryngeal nerve palsy 25.3%; hypoparathyroidism 6%). Recurrence of PC was observed in 32 of 83 cases. In univariate analysis, rate of recurrence was reduced when extended initial surgery had been performed (P = 0.04). In multivariate analysis low T status [odds ratio (OR) = 2.65, 95% confidence interval (CI) 1.02-6.88, P = 0.045], N0 stage at initial diagnosis (OR = 6.32, 95% CI 1.33-30.01, P = 0.02), Ki-67 <10% (OR = 14.07, 95% CI 2.09-94.9, P = 0.007), and postoperative biochemical remission (OR = 0.023, 95% CI 0.001-0.52, P = 0.018) were beneficial prognostic parameters for recurrence-free survival.
CONCLUSION
Despite a favorable overall prognosis, PC shows high rates of recurrence leading to repeated surgery and postoperative recurrent laryngeal nerve palsy and hypoparathyroidism. In view of the reduced recurrence rate in cases of extended surgery, ipsilateral completion surgery may be considered when PC is confirmed.

Identifiants

pubmed: 32649472
pii: 00000658-202202000-00055
doi: 10.1097/SLA.0000000000004144
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e479-e487

Informations de copyright

Copyright © 2020 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

The authors report no conflicts of interest.

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Auteurs

Christina Lenschow (C)

Department of General, Visceral, Transplant, Vascular and Pediatric Surgery, University Hospital Würzburg, Würzburg, Germany.

Sina Schrägle (S)

Department of General, Visceral, Transplant, Vascular and Pediatric Surgery, University Hospital Würzburg, Würzburg, Germany.

Stefan Kircher (S)

Institute of Pathology, University of Würzburg, Würzburg, Germany.

Kerstin Lorenz (K)

University Hospital Halle, Department of Visceral, Vascular, and Endocrine Surgery, Martin-Luther University of Halle-Wittenberg, Halle, Germany.

Andreas Machens (A)

University Hospital Halle, Department of Visceral, Vascular, and Endocrine Surgery, Martin-Luther University of Halle-Wittenberg, Halle, Germany.

Henning Dralle (H)

Department of General, Visceral and Transplantation Surgery, Section of Endocrine Surgery, University of Duisburg-Essen, Essen, Germany.

Philipp Riss (P)

University Hospital of Vienna, Department of Surgery, Vienna, Austria.

Christian Scheuba (C)

University Hospital of Vienna, Department of Surgery, Vienna, Austria.

Andreas Pfestroff (A)

University Hospital Marburg, Department of Nuclear Medicine, University Hospital Marburg, Germany.

Christine Spitzweg (C)

University Hospital Munich, Department of Internal Medicine IV, Ludwig-Maximilians-University Munich, Munich, Germany.

Andreas Zielke (A)

Diakonie Hospital Stuttgart, Depart for endocrine Surgery, Stuttgart, Germany.

Anna Nießen (A)

Heidelberg University Hospital, Department of General, Visceral and Transplantation Surgery, Heidelberg, Germany.

Cornelia Dotzenrath (C)

Helios University Hospital Wuppertal, Department of Endocrine Surgery, Wuppertal, Germany.

Burkhard Riemann (B)

University Hospital of Muenster, Department of Nuclear Medicine, Muenster, Germany.

Marcus Quinkler (M)

Endocrine Practice Berlin-Charlottenburg, Berlin, Germany.

Christian Vorländer (C)

Buergerhospital Frankfurt am Main, Department for Endocrine Surgery, Frankfurt, Germany.

Alexandra Zahn (A)

Schön-Klinik Hamburg, Department of Endocrine Surgery, Hamburg, Germany.

Friedhelm Raue (F)

Endocrine and Nuclear Practice Heidelberg, Heidelberg, Germany.

Costanza Chiapponi (C)

University Hospital Cologne, Department of General, - Visceral, Tumor and Transplantation Surgery, Colognen, Germany.

Karl Alexander Iwen (KA)

University Hospital Schleswig-Holstein Campus Lübeck, University MVZ Lübeck, Lübeck, Germany.

Thomas Steinmüller (T)

DRK-Hospital Berlin, Department of General, Visceral and Minimal invasive Surgery, Berlin, Germany.

Matthias Kroiss (M)

Department of Internal Medicine I, Division of Endocrinology and Diabetes, University Hospital Würzburg, Würzburg, Germany.
Comprehensive Cancer Center Wuerzburg, University Hospital Würzburg, Germany.

Nicolas Schlegel (N)

Department of General, Visceral, Transplant, Vascular and Pediatric Surgery, University Hospital Würzburg, Würzburg, Germany.

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