Long-term prognosis of primary retroperitoneal soft tissue sarcoma.

Th. Dalen; J.M. Plooij; F. van Coevorden; A.N. van Geel; H.J. Hoekstra; Ch Albus-Lutter; P.J. Slootweg; A. Hennipman

Long-term prognosis of primary retroperitoneal soft tissue sarcoma.

Translated title of the contribution: Long-term prognosis of primary retroperitoneal soft tissue sarcoma.

Th. Dalen
, J.M. Plooij
, F. van Coevorden
, A.N. van Geel
, H.J. Hoekstra
, Ch Albus-Lutter
, P.J. Slootweg
, A. Hennipman

Research output: Contribution to journal › Article › Academic › peer-review

Abstract

AIMS: To evaluate the result of treatment and long-term outcome of a population-based cohort of patients with retroperitoneal soft tissue sarcoma (RSTS). METHODS: Between 1 January 1989 and 1 January 1994, 143 patients diagnosed as having primary RSTS were selected from a national pathology database (PALGA) in the Netherlands. In this population-based group of patients, the result of surgery, overall survival (OS) and disease-free survival (DFS) were analysed as well as factors affecting OS and DFS. Median follow-up was 10.2 years. RESULTS: Operative treatment resulted in a complete tumour resection in 55% of the patients (n=78), low- and intermediate-grade tumours were more often completely resected than high-grade tumours (P=0.016). Five- and 10-year cumulative OS was 39% and 21%, respectively, while DFS was 22% and 17%, respectively. In a multivariate analysis low malignancy grade (P=0.017) and a complete tumour resection (P

Translated title of the contribution	Long-term prognosis of primary retroperitoneal soft tissue sarcoma.
Original language	Undefined/Unknown
Pages (from-to)	234-238
Number of pages	5
Journal	European Journal of Surgical Oncology
Volume	33
Issue number	2
Publication status	Published - 2007

Cite this

@article{21f0cb578fbe481e888135bafa5dcd5f,

title = "Long-term prognosis of primary retroperitoneal soft tissue sarcoma.",

abstract = "AIMS: To evaluate the result of treatment and long-term outcome of a population-based cohort of patients with retroperitoneal soft tissue sarcoma (RSTS). METHODS: Between 1 January 1989 and 1 January 1994, 143 patients diagnosed as having primary RSTS were selected from a national pathology database (PALGA) in the Netherlands. In this population-based group of patients, the result of surgery, overall survival (OS) and disease-free survival (DFS) were analysed as well as factors affecting OS and DFS. Median follow-up was 10.2 years. RESULTS: Operative treatment resulted in a complete tumour resection in 55\% of the patients (n=78), low- and intermediate-grade tumours were more often completely resected than high-grade tumours (P=0.016). Five- and 10-year cumulative OS was 39\% and 21\%, respectively, while DFS was 22\% and 17\%, respectively. In a multivariate analysis low malignancy grade (P=0.017) and a complete tumour resection (P",

author = "Th. Dalen and J.M. Plooij and \{van Coevorden\}, F. and \{van Geel\}, A.N. and H.J. Hoekstra and Ch Albus-Lutter and P.J. Slootweg and A. Hennipman",

year = "2007",

language = "Undefined/Unknown",

volume = "33",

pages = "234--238",

journal = "European Journal of Surgical Oncology",

issn = "0748-7983",

publisher = "W.B. Saunders Ltd",

number = "2",

}

TY - JOUR

T1 - Long-term prognosis of primary retroperitoneal soft tissue sarcoma.

AU - Dalen, Th.

AU - Plooij, J.M.

AU - van Coevorden, F.

AU - van Geel, A.N.

AU - Hoekstra, H.J.

AU - Albus-Lutter, Ch

AU - Slootweg, P.J.

AU - Hennipman, A.

PY - 2007

Y1 - 2007

N2 - AIMS: To evaluate the result of treatment and long-term outcome of a population-based cohort of patients with retroperitoneal soft tissue sarcoma (RSTS). METHODS: Between 1 January 1989 and 1 January 1994, 143 patients diagnosed as having primary RSTS were selected from a national pathology database (PALGA) in the Netherlands. In this population-based group of patients, the result of surgery, overall survival (OS) and disease-free survival (DFS) were analysed as well as factors affecting OS and DFS. Median follow-up was 10.2 years. RESULTS: Operative treatment resulted in a complete tumour resection in 55% of the patients (n=78), low- and intermediate-grade tumours were more often completely resected than high-grade tumours (P=0.016). Five- and 10-year cumulative OS was 39% and 21%, respectively, while DFS was 22% and 17%, respectively. In a multivariate analysis low malignancy grade (P=0.017) and a complete tumour resection (P

AB - AIMS: To evaluate the result of treatment and long-term outcome of a population-based cohort of patients with retroperitoneal soft tissue sarcoma (RSTS). METHODS: Between 1 January 1989 and 1 January 1994, 143 patients diagnosed as having primary RSTS were selected from a national pathology database (PALGA) in the Netherlands. In this population-based group of patients, the result of surgery, overall survival (OS) and disease-free survival (DFS) were analysed as well as factors affecting OS and DFS. Median follow-up was 10.2 years. RESULTS: Operative treatment resulted in a complete tumour resection in 55% of the patients (n=78), low- and intermediate-grade tumours were more often completely resected than high-grade tumours (P=0.016). Five- and 10-year cumulative OS was 39% and 21%, respectively, while DFS was 22% and 17%, respectively. In a multivariate analysis low malignancy grade (P=0.017) and a complete tumour resection (P

M3 - Article

SN - 0748-7983

VL - 33

SP - 234

EP - 238

JO - European Journal of Surgical Oncology

JF - European Journal of Surgical Oncology

IS - 2

ER -

Long-term prognosis of primary retroperitoneal soft tissue sarcoma.

Abstract

Fingerprint

Cite this