Cytoreductive surgery and hyperthermic intraperitoneal chemotherapy versus palliative systemic chemotherapy in stomach cancer patients with peritoneal dissemination, the study protocol of a multicentre randomised controlled trial (PERISCOPE II)
W. J. Koemans,
R. T. van der Kaaij,
H. Boot,
T. Buffart,
A. A. F. A. Veenhof,
K. J. Hartemink,
C. Grootscholten,
P. Snaebjornsson,
V. P. Retel,
H. van Tinteren,
S. Vanhoutvin,
V. van der Noort,
A. Houwink,
C. Hahn,
A. D. R. Huitema,
M. Lahaye,
M. Los,
P. van den Barselaar,
O. Imhof,
A. Aalbers,
G. M. van Dam,
B. van Etten,
B. P. L. Wijnhoven,
M. D. P. Luyer,
D. Boerma,
J. W. van Sandick
Affiliations
W. J. Koemans
Department of Surgery, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
R. T. van der Kaaij
Department of Surgery, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
H. Boot
Department of Gastro-Intestinal Oncology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
T. Buffart
Department of Gastro-Intestinal Oncology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
A. A. F. A. Veenhof
Department of Surgery, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
K. J. Hartemink
Department of Surgery, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
C. Grootscholten
Department of Gastro-Intestinal Oncology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
P. Snaebjornsson
Department of Pathology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
V. P. Retel
Department of Psychosocial Research and Epidomiology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
H. van Tinteren
Department of Biometrics, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
S. Vanhoutvin
Department of Biometrics, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
V. van der Noort
Department of Biometrics, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
A. Houwink
Department of Anaesthesiology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
C. Hahn
Department of Anaesthesiology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
A. D. R. Huitema
Department of Pharmacy & Pharmacology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
M. Lahaye
Department of Radiology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
M. Los
Department of Oncology, Sint Antonius Hospital
P. van den Barselaar
Clinical perfusion
O. Imhof
Clinical perfusion
A. Aalbers
Department of Surgery, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
G. M. van Dam
Department of Surgery, University Medical Center Groningen
B. van Etten
Department of Surgery, University Medical Center Groningen
B. P. L. Wijnhoven
Department of Surgery, Erasmus Medical Center
M. D. P. Luyer
Department of Surgery, Catharina Hospital
D. Boerma
Department of Surgery, Sint Antonius Hospital
J. W. van Sandick
Department of Surgery, The Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital
Abstract Background At present, palliative systemic chemotherapy is the standard treatment in the Netherlands for gastric cancer patients with peritoneal dissemination. In contrast to lymphatic and haematogenous dissemination, peritoneal dissemination may be regarded as locoregional spread of disease. Administering cytotoxic drugs directly into the peritoneal cavity has an advantage over systemic chemotherapy since high concentrations can be delivered directly into the peritoneal cavity with limited systemic toxicity. The combination of a radical gastrectomy with cytoreductive surgery (CRS) and hyperthermic intraperitoneal chemotherapy (HIPEC) has shown promising results in patients with gastric cancer in Asia. However, the results obtained in Asian patients cannot be extrapolated to Western patients. The aim of this study is to compare the overall survival between patients with gastric cancer with limited peritoneal dissemination and/or tumour positive peritoneal cytology treated with palliative systemic chemotherapy, and those treated with gastrectomy, CRS and HIPEC after neoadjuvant systemic chemotherapy. Methods In this multicentre randomised controlled two-armed phase III trial, 106 patients will be randomised (1:1) between palliative systemic chemotherapy only (standard treatment) and gastrectomy, CRS and HIPEC (experimental treatment) after 3–4 cycles of systemic chemotherapy.Patients with gastric cancer are eligible for inclusion if (1) the primary cT3-cT4 gastric tumour including regional lymph nodes is considered to be resectable, (2) limited peritoneal dissemination (Peritoneal Cancer Index < 7) and/or tumour positive peritoneal cytology are confirmed by laparoscopy or laparotomy, and (3) systemic chemotherapy was given (prior to inclusion) without disease progression. Discussion The PERISCOPE II study will determine whether gastric cancer patients with limited peritoneal dissemination and/or tumour positive peritoneal cytology treated with systemic chemotherapy, gastrectomy, CRS and HIPEC have a survival benefit over patients treated with palliative systemic chemotherapy only. Trial registration clinicaltrials.gov NCT03348150; registration date November 2017; first enrolment November 2017; expected end date December 2022; trial status: Ongoing.