A.J. Witkamp
Netherlands Cancer Institute
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Featured researches published by A.J. Witkamp.
Annals of Surgical Oncology | 2005
Vic J. Verwaal; Serge van Ruth; A.J. Witkamp; Henk Boot; Gooike W. van Slooten; F.A.N. Zoetmulder
AbstractBackgroundPeritoneal carcinomatosis of colorectal cancer is probably best treated by cytoreduction and hyperthermic intraperitoneal chemotherapy (HIPEC). In The Netherlands Cancer Institute, this treatment has been performed since 1995. The long tradition of this treatment enabled us to study long-term survival in detail.Methods Between 1995 and 2003, 117 patients were treated by cytoreduction and HIPEC. The aim of the cytoreduction was to remove all visible tumor. After the cytoreduction, the abdomen was perfused with mitomycin C (35 mg/m2) at 40°C to 41°C for 90 minutes. Survival was calculated by the Kaplan-Meier method. Survival was also analyzed for the following subgroups: no residual tumor, residual tumor ≤2.5 mm, and more residual tumor. Hazard ratios for each of the seven abdominal regions were calculated to determine the influence on survival.ResultsThe median survival was 21.8 months. The 1-, 3-, and 5-year survival rates were 75%, 28%, and 19%, respectively. The Kaplan-Meier curve reached a plateau of 18% at 54 months. In 59 patients a complete cytoreduction was achieved, and in 41 patients there was minimal residual disease. The median survival of these patient groups was 42.9 and 17.4 months, respectively. When gross macroscopic tumor was left behind, as was the case in 17 patients, the median survival was 5 months. Involvement of the small bowel before cytoreduction was associated with poorer outcome.Conclusions Cytoreduction followed by HIPEC showed a median survival of 21 months. From 3 years on, a consistent group of 18% of patients stayed alive.
European Journal of Cancer | 2001
A.J. Witkamp; E. de Bree; M.M. Kaag; Henk Boot; Jos H. Beijnen; G.W. van Slooten; F. van Coevorden; F.A.N. Zoetmulder
Peritoneal seeding from colorectal cancer has a very poor prognosis and is relatively resistant to systemic chemotherapy. We performed a phase I/II trial to investigate the feasibility and effectiveness of extensive cytoreductive surgery in combination with intra-operative hyperthermic intraperitoneal chemotherapy (HIPEC) in these patients. 29 patients with peritoneal carcinomatosis of colorectal origin without evidence of distant metastases underwent cytoreductive surgery and intra-operative HIPEC with mitomycin-C (MMC), followed by systemic chemotherapy with 5-fluorouracil (5-FU)/leucovorin. Surgical complications occurred in 11 patients (38%). One patient died directly related to the treatment, resulting in a mortality rate of 3%. MMC toxicity existed mainly of leucocytopenia (in 15 patients; 52%). After a median follow-up of 38 months (range 26-52 months) we found a 2- and 3-year survival rate (Kaplan-Meier) of 45 and 23%, respectively. Extensive cytoreductive surgery and HIPEC is feasible in patients with peritoneal seeding of colorectal cancer. First results suggest that a higher median survival could be achieved compared with conventional palliative surgery and systemic chemotherapy, therefore a randomised phase III study is now being conducted.
Journal of Surgical Oncology | 2000
Eelco de Bree; A.J. Witkamp; Mark van de Vijver; Frans Zoetmulde
Pseudomyxoma peritonei is a rare neoplastic condition in that gelatinous intraperitoneal fluid collections and mucinous implants on the peritoneal surfaces and omentum are found. The pathological origin is usually an adenoma or well‐differentiated adenocarcinoma of the appendix. A smaller number of cases arises from ovarian tumors. We report two unusual cases of pseudomyxoma peritonei. As a child, the first patient underwent several surgical procedures of the large bowel to relieve the consequences of Hirschsprung disease that were complicated by recurrent enteric fistulae. Colonic epithelial cells, with neoplastic changes due to chronic inflammation in the presence of enteric fistulae, were probably dislocated during these episodes, causing pseudomyxoma peritonei. In the second patient, pseudomyxoma was caused by intraperitoneal seeding of a mucinous urachal adenocarcinoma. We hypothesize that seeding of mucus producing epithelial cells into the abdominal cavity may result in this rare entity called pseudomyxoma peritonei, regardless of the source. J. Surg. Oncol. 2000;75:270–274.
Journal of Surgical Oncology | 2004
Eelco de Bree; Wim Koops; Robert Kröger; Serge van Ruth; A.J. Witkamp; F.A.N. Zoetmulder
Cancer Treatment Reviews | 2001
A.J. Witkamp; Eelco de Bree; R Van Goethem; F.A.N. Zoetmulder
British Journal of Surgery | 2001
A.J. Witkamp; E. de Bree; M.M. Kaag; G.W. van Slooten; F. van Coevorden; F.A.N. Zoetmulder
Chest | 2002
Eelco de Bree; Serge van Ruth; Paul Baas; Emiel J. Th. Rutgers; Nico van Zandwijk; A.J. Witkamp; F.A.N. Zoetmulder
Journal of Surgical Oncology | 2002
Eelco de Bree; A.J. Witkamp; F.A.N. Zoetmulder
Ejso | 2000
Eelco de Bree; A.J. Witkamp; F.A.N. Zoetmulder
Annals of Gastroenterology | 2003
John Romanos; A.J. Witkamp; Dimitris D. Tsiftsis; E. de Bree; F.A.N. Zoetmulder