Literature DB >> 24241953

[Surgical Management of Peritoneal Surface Malignancy with Respect to Tumour Type, Tumour Stage and Individual Tumour Biology].

S Beckert1, F Struller1, E-M Grischke2, J Glatzle1, D Zieker1, A Königsrainer1, I Königsrainer1.   

Abstract

Peritoneal tumour dissemination is still considered as a terminal disease. For the last two decades, cytoreductive surgery (CRS) combined with intraoperative hyperthermic chemotherapy (HIPEC) has been popularised by Paul Sugarbaker almost doubling survival in selected patients compared with systemic chemotherapy alone. Nowadays, this particular treatment protocol is available in comprehensive cancer centres with reasonable mortality and morbidity. However, patient selection is still challenging. In general, CRS and HIPEC is indicated in primary peritoneal tumours such as mesothelioma and pseudomyxoma peritonei as well as in peritoneal metastases derived from gastrointestinal malignancies and ovarian cancers. Since systemic tumour spread is uncommon in patients with peritoneal metastases, peritoneal tumour dissemination was defined as localised disease within the "compartment abdomen". However, CRS and HIPEC are only beneficial as long as complete cytoreduction is achieved (CC-0 or CC-1). Histopathological parameters, the Sugarbaker peritoneal carcinomatosis index (PCI) and general condition of the patient have been established as patient selection criteria. In primary peritoneal cancers, individual tumour biology is the predominant criterium for patient selection as opposed to intraabdominal tumour load in peritoneal metastases derived from gastrointestinal cancers. In gastric cancer, CRS and HIPEC should be restricted to synchronous limited disease because of its biological aggressiveness. In patients with free floating cancer cells without macroscopic signs of peritoneal spread, however, CRS and HIPEC following preoperative "neoadjuvant" chemotherapy preserves chances for cure. So far, there is no general recommendation for CRS and HIPEC by clinical practice guidelines. In the recent S3 guideline for treatment of colorectal cancer, however, CRS and HIPEC have been included as possible treatment options. Georg Thieme Verlag KG Stuttgart · New York.

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Year:  2013        PMID: 24241953     DOI: 10.1055/s-0033-1350857

Source DB:  PubMed          Journal:  Zentralbl Chir        ISSN: 0044-409X            Impact factor:   0.942


  5 in total

1.  Randomized control trial comparing quality of life of patients with end-stage peritoneal metastasis treated with pressurized intraperitoneal aerosol chemotherapy (PIPAC) and intravenous chemotherapy.

Authors:  S P Somashekhar; K R Ashwin; C Amit Rauthan; Kumar C Rohit
Journal:  Pleura Peritoneum       Date:  2018-09-26

2.  Pressurized intraperitoneal aerosol chemotherapy procedure for nonresectable peritoneal carcinomatosis: First Indian study.

Authors:  S P Somashekhar; K R Ashwin; C Rohit Kumar; Amit Rauthan; Sushmita H Rakshit
Journal:  South Asian J Cancer       Date:  2019 Jan-Mar

3.  Pressurized intraperitoneal aerosol chemotherapy (PIPAC) in combination with standard of care chemotherapy in primarily untreated chemo naïve upper gi-adenocarcinomas with peritoneal seeding - a phase II/III trial of the AIO/CAOGI/ACO.

Authors:  Thorsten Oliver Goetze; Salah-Eddin Al-Batran; Urs Pabst; Marc Reymond; Clemens Tempfer; Wolf O Bechstein; Ulli Bankstahl; Ines Gockel; Alfred Königsrainer; Thomas Kraus; Stefan P Mönig; Beate Rau; Matthias Schwarzbach; Pompiliu Piso
Journal:  Pleura Peritoneum       Date:  2018-06-08

4.  Pressurized intraperitoneal aerosol chemotherapy (PIPAC) as a neoadjuvant therapy before cytoreductive surgery and hyperthermic intraperitoneal chemotherapy.

Authors:  Ramy Girshally; Cedric Demtröder; Nurettin Albayrak; Jürgen Zieren; Clemens Tempfer; Marc A Reymond
Journal:  World J Surg Oncol       Date:  2016-09-27       Impact factor: 2.754

5.  Different Features of Tumor-Associated NK Cells in Patients With Low-Grade or High-Grade Peritoneal Carcinomatosis.

Authors:  Silvia Pesce; Valerio Belgrano; Marco Greppi; Simona Carlomagno; Margherita Squillario; Annalisa Barla; Mariella Della Chiesa; Stefano Di Domenico; Domenico Mavilio; Lorenzo Moretta; Simona Candiani; Simona Sivori; Franco De Cian; Emanuela Marcenaro
Journal:  Front Immunol       Date:  2019-08-21       Impact factor: 7.561

  5 in total

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