Evidence map›Paper›PMID 41000447›Full record

ArticlePleura and peritoneum2025

Real-world data on Pressurized IntraPeritoneal Aerosol Chemotherapy (PIPAC)-directed therapy in patients with peritoneal metastases; Third annual report from the ISSPP PIPAC database.

Magnus Skov Jørgensen, Pernille Schjødt Hansen, Claus W Fristrup, Martin Hübner, Jimmy So, Anne-Cecile Ezanno, Peter Hewett, Miguel Ruiz-Marin, Günther A Rezniczek, Özgül Düzgün and 11 more

Abstract read
In one paragraph

Article in Pleura and peritoneum, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Magnus Skov JørgensenOdense PIPAC Center (OPC) and Odense Pancreas Center (OPAC), Odense University Hospital, Odense, Denmark.ORCID https://orcid.org/0009-0002-4358-6796
Pernille Schjødt HansenOdense PIPAC Center (OPC) and Odense Pancreas Center (OPAC), Odense University Hospital, Odense, Denmark.ORCID https://orcid.org/0009-0001-9615-8704
Claus W FristrupOdense PIPAC Center (OPC) and Odense Pancreas Center (OPAC), Odense University Hospital, Odense, Denmark.ORCID https://orcid.org/0000-0003-2721-0967
Martin HübnerLausanne University Hospital CHUV, University of Lausanne (UNIL), Lausanne, Switzerland.
Jimmy SoSurgery, National University Hospital, Singapore, Singapore.
Anne-Cecile EzannoDepartment of Surgery, Hôpital d'Instruction des armées Begin, Saint-Mande, France.ORCID https://orcid.org/0000-0003-0270-5090
Peter HewettDepartment of Surgery, The Queen Elizabeth Hospital, Woodville South, South Australia, Australia.
Miguel Ruiz-MarinDepartment of Surgery, Reina Sofia University General Hospital, Murcia, Spain.
Günther A RezniczekObstetrics & Gynecology, Marien Hospital Herne, Klinikum der Ruhr-Universität Bochum, Herne, Germany.ORCID https://orcid.org/0000-0002-0852-6002
Özgül DüzgünDepartment of Surgical Oncology, İstanbul Ümraniye Training and Research Hospital, Istanbul, Türkiye.
Marc PocardDepartment of Digestive, Hepatobiliary Surgery and Liver Transplantation, Pitié-Salpêtrière Hospital, Assistance publique-Hôpitaux de Paris, Paris, France.ORCID https://orcid.org/0000-0002-4793-0008
Francesco CasellaGeneral and Upper GI Surgery, University of Verona, Verona, Veneto, Italy.
Laura LayDepartment of Gynecology Surgical Area at the Institute of Oncology A. H. Roffo, University of Buenos Aires, Buenos Aires, Argentina.
Marisa AralGeneral Surgery Department, Centro Hospitalar Universitário de São João, Porto, Portugal.
Tarkan JägerDepartment of Surgery, Paracelsus Medical University, Salzburg, Austria.
Felix LamingerDepartment of Surgery, Center for Peritoneal Carcinomatosis, Hanusch-Krankenhaus, Vienna, Austria.
Oliver GlehenService de Chirurgie Digestive et Oncologique, Hôpital Lyon Sud, Hospices Civils de Lyon, Lyon, France.
Claire-Angéline GoutardService de Chirurgie Digestive et Oncologique, Hôpital Lyon Sud, Hospices Civils de Lyon, Lyon, France.
Laurent VilleneuveService de Chirurgie Digestive et Oncologique, Hôpital Lyon Sud, Hospices Civils de Lyon, Lyon, France.ORCID https://orcid.org/0000-0002-8713-7821
Andrea Di GiorgioSurgical Unit of Peritoneum and Retroperitoneum, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Michael Bau MortensenOdense PIPAC Center (OPC) and Odense Pancreas Center (OPAC), Odense University Hospital, Odense, Denmark.ORCID https://orcid.org/0000-0002-7270-5005

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: In 2020, the International Society for the Study of the Pleura and Peritoneum (ISSPP) launched a database monitoring real-world data on Pressurized IntraPeritoneal Aerosol Chemotherapy (PIPAC)-directed therapy in patients with peritoneal metastases (PM). This study covers data from the third annual report on the ISSPP PIPAC database. Methods: Systematic analysis of all data reported to the ISSPP PIPAC database between June 15th, 2020, and November 1st, 2024. We hypothesize that ISSPP PIPAC data align with existing literature. Results: Seventeen PIPAC centers reported 3224 PIPAC treatments in 1126 patients with PM (median number of treatments 2, range 1-33). The median peritoneal cancer index (PCI) at PIPAC 1 was 19 and remained unchanged during subsequent treatments. The number of patients with >500 mL ascites significantly decreased from the first three PIPAC treatments to PIPAC 4+ (p<0.01). Major complications (Dindo-Clavien ≥3b) occurred in 0.7 % of the treatments, while Common. Terminology Criteria for Adverse Events (CTCAE) grades ≥3 were reported in 5.2 %. Peritoneal regression grading score (PRGS) was performed in 2306 (72 %) of the treatments. At PIPAC 1, 2, and 3, complete or major response (mean PRGS ≤2) was achieved in 57 %, 72 %, and 75 % of the patients, respectively. Median overall survival from PIPAC 1 was 12.5 months. Patients with complete/major response (mean PRGS ≤2) at PIPAC 1-3 had a longer overall survival compared to patients with minimal/no response (mean PRGS >2). Conclusions: This study from the ISSPP PIPAC database provides substantial real-world data demonstrating the feasibility, safety, and potential effect of PIPAC-directed therapy in patients with PM.

Indexed as

databaseISSPPperitoneal metastasisPIPAC

Identifiers

PMID41000447
PMCPMC12458025

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.