Incidence and Outcomes of Desmoplastic Small Round Cell Tumor: Results from the Surveillance, Epidemiology, and End Results Database

Desmoplastic small round cell tumor (DSRCT) is a rare but highly fatal malignancy. Due to the rarity of this neoplasm, no large population based studies exist. Procedure. This is a retrospective cohort analysis. Incidence rates were calculated based on sex and ethnicity and compared statistically....

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Main Authors: Christina K. Lettieri, Pamela Garcia-Filion, Pooja Hingorani
Format: Article
Language:English
Published: Hindawi Limited 2014-01-01
Series:Journal of Cancer Epidemiology
Online Access:http://dx.doi.org/10.1155/2014/680126
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spelling doaj-9d73c10d676c4f94a78cbcd92ba861eb2020-11-24T23:58:10ZengHindawi LimitedJournal of Cancer Epidemiology1687-85581687-85662014-01-01201410.1155/2014/680126680126Incidence and Outcomes of Desmoplastic Small Round Cell Tumor: Results from the Surveillance, Epidemiology, and End Results DatabaseChristina K. Lettieri0Pamela Garcia-Filion1Pooja Hingorani2Children’s Hospital and Medical Center, Omaha, University of Nebraska Medical Center, 8200 Dodge Street, Omaha, NE 68114, USAPhoenix Children’s Hospital, 1919 E. Thomas Road, Phoenix, AZ 85006, USAPhoenix Children’s Hospital, 1919 E. Thomas Road, Phoenix, AZ 85006, USADesmoplastic small round cell tumor (DSRCT) is a rare but highly fatal malignancy. Due to the rarity of this neoplasm, no large population based studies exist. Procedure. This is a retrospective cohort analysis. Incidence rates were calculated based on sex and ethnicity and compared statistically. Gender-, ethnicity-, and treatment- based survival were calculated using the Kaplan-Meier method. Results. A total of 192 cases of DSRCT were identified. Peak incidence age was between 20 and 24 years. Age-adjusted incidence rate for blacks was 0.5 cases/million and for whites was 0.2 cases/million (P=0.037). There was no statistically significant difference in survival based on gender or ethnicity. When adjusted for age, there was no statistically significant difference in survival amongst patients who received radiation therapy compared to those who did not (HRadj = 0.73; 95% CI 0.49, 1.11). There was a statistically significant survival advantage for patients who received radiation after surgery compared to those who did not (HR 0.49; 95% CI 0.30, 0.79). Conclusion. DSRCT is more common in males and in people of African-American descent. Although overall survival remains poor, radiation therapy following surgery seems to improve outcome in these patients.http://dx.doi.org/10.1155/2014/680126
collection DOAJ
language English
format Article
sources DOAJ
author Christina K. Lettieri
Pamela Garcia-Filion
Pooja Hingorani
spellingShingle Christina K. Lettieri
Pamela Garcia-Filion
Pooja Hingorani
Incidence and Outcomes of Desmoplastic Small Round Cell Tumor: Results from the Surveillance, Epidemiology, and End Results Database
Journal of Cancer Epidemiology
author_facet Christina K. Lettieri
Pamela Garcia-Filion
Pooja Hingorani
author_sort Christina K. Lettieri
title Incidence and Outcomes of Desmoplastic Small Round Cell Tumor: Results from the Surveillance, Epidemiology, and End Results Database
title_short Incidence and Outcomes of Desmoplastic Small Round Cell Tumor: Results from the Surveillance, Epidemiology, and End Results Database
title_full Incidence and Outcomes of Desmoplastic Small Round Cell Tumor: Results from the Surveillance, Epidemiology, and End Results Database
title_fullStr Incidence and Outcomes of Desmoplastic Small Round Cell Tumor: Results from the Surveillance, Epidemiology, and End Results Database
title_full_unstemmed Incidence and Outcomes of Desmoplastic Small Round Cell Tumor: Results from the Surveillance, Epidemiology, and End Results Database
title_sort incidence and outcomes of desmoplastic small round cell tumor: results from the surveillance, epidemiology, and end results database
publisher Hindawi Limited
series Journal of Cancer Epidemiology
issn 1687-8558
1687-8566
publishDate 2014-01-01
description Desmoplastic small round cell tumor (DSRCT) is a rare but highly fatal malignancy. Due to the rarity of this neoplasm, no large population based studies exist. Procedure. This is a retrospective cohort analysis. Incidence rates were calculated based on sex and ethnicity and compared statistically. Gender-, ethnicity-, and treatment- based survival were calculated using the Kaplan-Meier method. Results. A total of 192 cases of DSRCT were identified. Peak incidence age was between 20 and 24 years. Age-adjusted incidence rate for blacks was 0.5 cases/million and for whites was 0.2 cases/million (P=0.037). There was no statistically significant difference in survival based on gender or ethnicity. When adjusted for age, there was no statistically significant difference in survival amongst patients who received radiation therapy compared to those who did not (HRadj = 0.73; 95% CI 0.49, 1.11). There was a statistically significant survival advantage for patients who received radiation after surgery compared to those who did not (HR 0.49; 95% CI 0.30, 0.79). Conclusion. DSRCT is more common in males and in people of African-American descent. Although overall survival remains poor, radiation therapy following surgery seems to improve outcome in these patients.
url http://dx.doi.org/10.1155/2014/680126
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