A. Hennipman
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Featured researches published by A. Hennipman.
Annals of Surgical Oncology | 2004
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
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
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
Th. van Dalen; Harald J. Hoekstra; A.N. van Geel; F. van Coevorden; Ch. Albus-Lutter; P.J. Slootweg; A. Hennipman
Ejso | 2001
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
Th. van Dalen; C.H.F. Gimbrere; A. Hennipman
Ejc Supplements | 2003
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
T. van Dalen; Hj Hoekstra; F. van Coevorden; A.N. van Geel; A. Hennipman
European Journal of Cancer | 2001
T. van Dalen; F. van Coevorden; A.N. van Geel; Hj Hoekstra; A. Hennipman
European Journal of Cancer | 1999
Th. van Dalen; F. van Coevorden; A.N. van Geel; Hj Hoekstra; A. Hennipman