Evidence map›Paper›PMID 30911656›Full record

ArticlePleura and peritoneum2018

Treatment of peritoneal carcinomatosis with Pressurized IntraPeritoneal Aerosol Chemotherapy - PIPAC-OPC2.

Martin Graversen, Sönke Detlefsen, Jon Asmussen, Bassam Mahdi, Claus Fristrup, Per Pfeiffer, Michael Bau Mortensen

Registry-linked trialOpen access · diamondAbstract read
In one paragraph

Article in Pleura and peritoneum, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03287375 (Treatment of Peritoneal Carcinomatosis With Pressurized IntraPeritoneal Aerosol - The PIPAC-OPC2 Trial), which is not on this map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 6% of its field
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.

NCT03287375 phase2completednot on this map

Treatment of Peritoneal Carcinomatosis With Pressurized IntraPeritoneal Aerosol - The PIPAC-OPC2 Trial

TypeinterventionalSponsorMichael Bau MortensenRan2016 to 2022Enrolled143ConditionsPeritoneum, Carcinomatosis, Peritoneal Neoplasms, Peritoneal MetastasesArmsPIPAC
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

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  7. Neoplastic appendiceal mucinous lesions: a narrative review of the literature from an oncologist's perspective.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
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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

7 authors at 1 institution in 1 country.

Martin GraversenOdense PIPAC Center (OPC) and Odense Pancreas Center (OPAC) HPB and Upper GI Section, Department of Surgery, Odense University Hospital, Odense, Denmark.
Sönke DetlefsenOdense PIPAC Center (OPC) and Odense Pancreas Center (OPAC), Department of Pathology, Odense University Hospital, Odense, Denmark.
Jon AsmussenOdense PIPAC Center (OPC) and Odense Pancreas Center (OPAC), Department of Radiology, Odense University Hospital, Odense, Denmark.
Bassam MahdiOdense PIPAC Center (OPC) and Odense Pancreas Center (OPAC), Department of Radiology, Odense University Hospital, Odense, Denmark.
Claus FristrupOdense PIPAC Center (OPC) and Odense Pancreas Center (OPAC) HPB and Upper GI Section, Department of Surgery, Odense University Hospital, Odense, Denmark.
Per PfeifferOdense PIPAC Center (OPC) and Odense Pancreas Center (OPAC), Department of Oncology, Odense University Hospital, Odense, Denmark.
Michael Bau MortensenOdense PIPAC Center (OPC) and Odense Pancreas Center (OPAC) HPB and Upper GI Section, Department of Surgery, Odense University Hospital, Odense, Denmark.
Odense University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPeritoneal carcinomatosis (PC) is a common endpoint in both gastrointestinal and non-gastrointestinal cancers, and PC is treated as other systemic metastases - unfortunately with disappointing results and considerable side-effects. Pressurized IntraPeritoneal Aerosol Chemotherapy (PIPAC) is a new method of applying traditional chemotherapy, and preliminary data indicate that PIPAC is safe, able to stabilize or improve quality of life, and can induce an objectively measurable reduction in disease burden in PC.

methodsPIPAC-OPC2 is a prospectively controlled Phase II, single center, one-arm, open-label clinical trial investigating the treatment effect of PIPAC in patients with histological or cytological proven PC from gastrointestinal, ovarian or primary peritoneal cancer. Eligible patients will receive PIPAC in series of three using a combination of doxorubicin (1.5 mg/m

resultsThe primary outcome of PIPAC-OPC2 is to evaluate if PIPAC can induce major or complete response (PRGS 1 or 2) within a series of three PIPAC procedures. Secondarily this study investigates changes in QoL and MRI as a staging and response evaluation tool. The secondary outcomes will be used to create a model that may predict which of the patients will benefit from PIPAC treatment.

conclusionsIt is expected that PIPAC directed therapy can induce major or complete response in 50 % of patients with PC of colorectal origin and in 30 % of patients with PC of non-colorectal origin - and at the same time stabilize or even improve quality of life. This trial may provide data regarding the utility of MRI as a staging and response evaluation tool in patients with PC.

trial registrationThe study is registered with ClinicalTrials.gov Identifier NCT03287375 and the European Clinical Trials Database (EudraCT) number 2016-003394-18.

Indexed as

MRIperitoneal carcinomatosisperitoneal regression grading score (PRGS)PIPACquality of liferesponse evaluation.

Identifiers

PMID30911656
PMCPMC6404994
OpenAlexW2807828774

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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 OpenQuestion graph.