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Dive into the research topics where A. Hennipman is active.

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Featured researches published by A. Hennipman.


Annals of Surgical Oncology | 2004

Evaluation of a clinically applicable post-surgical classification system for primary retroperitoneal soft-tissue sarcoma.

T. van Dalen; A. Hennipman; F. van Coevorden; H.J. Hoekstra; B.N. van Geel; P.J. Slootweg; C.F. Lutter; Murray F. Brennan; S. Singer

Background: The present AJCC/TNM staging system is of limited value for prediction of prognosis for patients with retroperitoneal sarcoma. The objective of the present study was to develop a postsurgical classification system that would enable comparison of outcomes for patients with primary retroperitoneal soft-tissue sarcoma.Methods: Four classes were defined: I, low-grade/complete resection/no metastasis; II, high-grade/complete resection/no metastasis; III, any-grade/incomplete resection/no metastasis; and IV, any-grade/any resection/distant metastasis. The prognostic value of this classification system was analyzed in a population-based multicenter group(MCG) of patients with primary retroperitoneal soft-tissue sarcoma (n = 124) and in a cohort of patients treated in a single tertiary referral center (SCG; n = 107).Results: Overall 5-year survival rates were 55% in the SCG and 43% in the MCG (P = 0.02). Class III (incomplete resection) was more frequent in the MCG than in the SCG (33% vs. 16%; P = 0.02). In the SCG, stage-specific 5-year survival rates were 89%, 40%, 26%, and 17% for classes I, II, III, and IV, respectively (P < 0.001), in comparison with 68%, 46%, 24%, and 0% in the MCG (P < 0.001). In a comparison of class-specific survival between the groups, only class I patients in the SCG had significantly better survival than class I patients in the MCG (P = 0.048).Conclusions: Classification based on grade, completeness of resection, and distant metastasis offers a reproducible prognostic tool that can be used to evaluate treatment strategies for primary retroperitoneal soft-tissue sarcoma. The probability of complete resection was significantly higher in the SCG than in the MCG. In patients with low-grade, completely resected sarcoma, there is a significant survival benefit with treatment in a high-volume tertiary center of excellence.


Ejso | 2010

Current pathology work-up of extremity soft tissue sarcomas, evaluation of the validity of different techniques

P. Verheijen; H. Witjes; J. van Gorp; A. Hennipman; T. van Dalen

OBJECTIVE In patients with extremity soft tissue sarcomas (STSs) a correct histopathological diagnosis is considered important before surgical treatment. We evaluated the preoperative use and sensitivity of the various pathology techniques. METHODS In a population-based study in patients operated for a newly diagnosed extremity STS between January 2000 and December 2003 the preoperative pathology work-up was evaluated. Data were retrieved from a national pathology database (PALGA). The sensitivity of the three techniques was assessed considering an examination affirmative when the conclusion of the pathology report stated the presence of mesenchymal malignancy. RESULTS The pathology reports of 573 patients were identified in the database. In 177 patients (31%) no pathology examination was done before resection of the tumour. In the remaining 396 patients the pathology procedure of first choice had been an incisional biopsy (IB) in 195 patients (49%), a core-needle biopsy (CNB) in 90 patients (23%) and a fine needle aspiration (FNA) in 111 patients (28%). An affirmative diagnosis was established in 95% of the patients following an IB, in 78% after a CNB and in 38% following FNA. After an initial CNB an additional IB was performed in 18 of the 90 patients improving the yield to 89%. After an initial FNA a subsequent histological biopsy was done in 53 of the 111 patients, increasing the sensitivity to 71%. CONCLUSIONS In this population-based study in patients treated for extremity STS, the proportion of patients operated without preoperative pathology evaluation was high. In the remaining patients an incisional biopsy was still the most commonly performed technique with the highest yield.


Ejso | 2007

Long-term prognosis of primary retroperitoneal soft tissue sarcoma

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


Ejso | 2001

Locoregional recurrence of retroperitoneal soft tissue sarcoma: second chance of cure for selected patients

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


Ejso | 2001

Soft tissue sarcoma in the retroperitoneum: an often neglected diagnosis

Th. van Dalen; A.N. van Geel; F. van Coevorden; Harald J. Hoekstra; Ch. Albus-Lutter; P.J. Slootweg; J.W.W. Coebergh; A. Hennipman


European Journal of Cancer | 1999

Epidemiological aspects of soft tissue sarcoma in the retroperitoneum in comparison to other anatomical sites

Th. van Dalen; C.H.F. Gimbrere; A. Hennipman


Ejc Supplements | 2003

698 Evaluation of a clinically applicable post-surgical classification system for primary retroperitoneal soft tissue sarcoma

T. van Dalen; A. Hennipman; F. van Coevorden; Hj Hoekstra; A.N. van Geel; P.J. Slootweg; Ch.F. Albus Lutter; Murray F. Brennan; S. Singer


European Journal of Cancer | 2001

Factors predicting survival of patients with retroperitoneal soft-tissue sarcoma; does surgical experience influence survival?

T. van Dalen; Hj Hoekstra; F. van Coevorden; A.N. van Geel; A. Hennipman


European Journal of Cancer | 2001

A biopsy of a suspected soft tissue sarcoma in the retroperitoneal space; the diagnostic yield and the risk of contamination of the different procedures

T. van Dalen; F. van Coevorden; A.N. van Geel; Hj Hoekstra; A. Hennipman


European Journal of Cancer | 1999

Retroperitoneal soft tissue sarcoma: a difficult diagnosis

Th. van Dalen; F. van Coevorden; A.N. van Geel; Hj Hoekstra; A. Hennipman

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A.N. van Geel

Erasmus University Rotterdam

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F. van Coevorden

Netherlands Cancer Institute

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Hj Hoekstra

University of Groningen

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Ch. Albus-Lutter

Netherlands Cancer Institute

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Murray F. Brennan

Memorial Sloan Kettering Cancer Center

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S. Singer

Memorial Sloan Kettering Cancer Center

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Harald J. Hoekstra

University Medical Center Groningen

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