Outcome of patients with peritoneal metastasis from ovarian cancer treated with Pressurized IntraPeritoneal Aerosol Chemotherapy (PIPAC)

Author:

Foslund Ingrid Terese12,von Magius Sahra Aisha Vinholt12,Ainsworth Alan Patrick134,Detlefsen Sönke145ORCID,Fristrup Claus Wilki13,Knudsen Anja Oer16,Mortensen Michael Bau134ORCID,Tarpgaard Line Schmidt146,Jochumsen Kirsten Marie24,Graversen Martin1347

Affiliation:

1. Odense PIPAC Centre , 11286 Odense University Hospital , Odense , Denmark

2. Department of Obstetrics and Gynaecology , 11286 Odense University Hospital , Odense , Denmark

3. Department of Surgery , 11286 Odense University Hospital , Odense , Denmark

4. Department of Clinical Research , Faculty of Health Sciences, University of Southern Denmark , Odense , Denmark

5. Department of Pathology , 11286 Odense University Hospital , Odense , Denmark

6. Department of Oncology , 11286 Odense University Hospital , Odense , Denmark

7. OPEN – Open Patient Data Explorative Network , 11286 Odense University Hospital , Odense , Denmark

Abstract

Abstract Objectives There are few data on Pressurized IntraPeritoneal Aerosol Chemotherapy with cisplatin and doxorubicin (PIPAC C/D) in women with primary unresectable or recurrent platinum-resistant peritoneal metastasis (PM) from ovarian cancer (OC). We evaluated survival, histological and cytological response, Quality of Life (QoL) and toxicity after PIPAC C/D in these patients. Methods Retrospective analysis of patients from the prospective PIPAC-OPC1 and -OPC2 studies. The histological response was evaluated by the Peritoneal Regression Grading Score (PRGS). QoL questionnaires were collected at baseline and after third PIPAC or 60 days. Adverse events were collected until 30 days after the last PIPAC. Demographic and survival data were analysed based on intention to treat. Response, QoL and toxicity were analysed per protocol (≥1 PIPAC). Results Twenty-nine patients were included. Five patients (17 %) were non-accessible at PIPAC 1. One patient was excluded due to liver metastases at PIPAC 1. Thus, 23 patients had 76 PIPACs (median 2, range 1–12). Median overall survival was 8.2 months (95 % CI 4.4–10.3) from PIPAC 1. Biopsy data were available for 22 patients, and seven (32 %) patients had a major/complete histological response (PRGS≤2) at PIPAC 3. No cytological conversions were registered. Symptoms and function scores worsened, while emotional scores improved. Three patients had severe adverse reactions (two ileus, one pulmonary embolism); no life-threatening reactions or treatment-related mortality was observed. Conclusions PIPAC C/D was feasible and induced histological regression in a substantial proportion of patients with platinum-resistant PM from OC. Larger studies are needed to evaluate impact on survival.

Publisher

Walter de Gruyter GmbH

Reference41 articles.

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