Increased risk of second primary hematologic and solid malignancies in patients with mycosis fungoides: A Surveillance, Epidemiology, and End Results analysis.


Journal

Journal of the American Academy of Dermatology
ISSN: 1097-6787
Titre abrégé: J Am Acad Dermatol
Pays: United States
ID NLM: 7907132

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 15 02 2019
revised: 11 07 2019
accepted: 24 07 2019
pubmed: 3 8 2019
medline: 24 2 2021
entrez: 3 8 2019
Statut: ppublish

Résumé

Mycosis fungoides (MF) is associated with increased risk of second primary hematologic malignancies, but its association with second primary solid tumors is less well characterized. This retrospective analysis seeks to assess the risk of being diagnosed with a second primary hematologic or solid malignancy in patients with MF. We performed an analysis of patients diagnosed with MF from 2000 through 2015 in the United States cancer registries of SEER-18 (N = 6742). Relative risks were estimated by using standardized incidence ratios (SIRs). Among 6742 patients, there were 511 (7.5%) second cancer events (SIR, 10.15; 95% confidence interval [CI], 9.29-11.07). These included 184 (36.0%) hematologic malignancies (SIR, 39.71; 95% CI, 34.05-46.05) and 327 (64.0%) solid tumor malignancies (SIR, 7.33; 95% CI, 6.56-8.17). Patients with MF were at increased risk for non-Hodgkin lymphoma; Hodgkin lymphoma; melanoma; and lung, female breast, prostate, colon, and renal cancers. Females were at higher risk than males (P < .05). All ethnic groups showed a statistically significant elevation in SIRs. Elevation of SIRs was observed across all stages of MF. Patients with MF are at increased risk for diagnosis of second primary malignancies and should be carefully screened for discernable signs and symptoms of second malignancies.

Sections du résumé

BACKGROUND BACKGROUND
Mycosis fungoides (MF) is associated with increased risk of second primary hematologic malignancies, but its association with second primary solid tumors is less well characterized.
OBJECTIVE OBJECTIVE
This retrospective analysis seeks to assess the risk of being diagnosed with a second primary hematologic or solid malignancy in patients with MF.
DESIGN METHODS
We performed an analysis of patients diagnosed with MF from 2000 through 2015 in the United States cancer registries of SEER-18 (N = 6742).
RESULTS RESULTS
Relative risks were estimated by using standardized incidence ratios (SIRs). Among 6742 patients, there were 511 (7.5%) second cancer events (SIR, 10.15; 95% confidence interval [CI], 9.29-11.07). These included 184 (36.0%) hematologic malignancies (SIR, 39.71; 95% CI, 34.05-46.05) and 327 (64.0%) solid tumor malignancies (SIR, 7.33; 95% CI, 6.56-8.17). Patients with MF were at increased risk for non-Hodgkin lymphoma; Hodgkin lymphoma; melanoma; and lung, female breast, prostate, colon, and renal cancers. Females were at higher risk than males (P < .05). All ethnic groups showed a statistically significant elevation in SIRs. Elevation of SIRs was observed across all stages of MF.
CONCLUSIONS AND RELEVANCE CONCLUSIONS
Patients with MF are at increased risk for diagnosis of second primary malignancies and should be carefully screened for discernable signs and symptoms of second malignancies.

Identifiants

pubmed: 31374302
pii: S0190-9622(19)32466-1
doi: 10.1016/j.jaad.2019.07.075
pmc: PMC7021276
mid: NIHMS1055619
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

404-411

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR002494
Pays : United States

Informations de copyright

Copyright © 2019 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.

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Auteurs

Amrita Goyal (A)

Department of Dermatology, University of Minnesota, Minneapolis, Minnesota. Electronic address: goyal046@umn.edu.

Daniel O'Leary (D)

Department of Medicine, University of Minnesota, Minneapolis, Minnesota; Division of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota, Minneapolis, Minnesota.

Kavita Goyal (K)

Department of Dermatology, University of Minnesota, Minneapolis, Minnesota.

Nathan Rubin (N)

Biostatistics Core, Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota.

Kimberly Bohjanen (K)

Department of Dermatology, University of Minnesota, Minneapolis, Minnesota.

Maria Hordinsky (M)

Department of Dermatology, University of Minnesota, Minneapolis, Minnesota.

Steven T Chen (ST)

Department of Dermatology, Massachusetts General Hospital, Boston, Massachusetts.

Georgios Pongas (G)

Division of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota, Minneapolis, Minnesota.

Lyn M Duncan (LM)

Dermatopathology Unit, Department of Pathology, Massachusetts General Hospital, Boston, Massachusetts.

Aleksandr Lazaryan (A)

Department of Hematology-Oncology, Moffitt Cancer Center, Tampa, Florida.

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