Evidence map›Paper›PMID 40740309›Full record

ArticleSurgical oncology insight2025

Outcomes following diagnostic laparoscopy in patients with peritoneal carcinomatosis deemed ineligible for cytoreduction and hyperthermic intraperitoneal chemotherapy (HIPEC) due to disease burden.

Paula Marincola Smith, Ashlee Seldomridge, Yi-Ju Chiang, Michael G White, Yun Song, Christopher Scally, Paul F Mansfield, Keith F Fournier, Beth A Helmink

Abstract read
In one paragraph

Article in Surgical oncology insight, 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. Article
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

9 authors.

Paula Marincola SmithDepartment of Surgical Oncology, Division of Surgery, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Ashlee SeldomridgeDepartment of Surgical Oncology, Division of Surgery, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Yi-Ju ChiangDepartment of Surgical Oncology, Division of Surgery, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Michael G WhiteDepartment of Colorectal Surgery, Division of Surgery, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Yun SongDepartment of Surgical Oncology, Division of Surgery, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Christopher ScallyDepartment of Surgical Oncology, Division of Surgery, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Paul F MansfieldDepartment of Surgical Oncology, Division of Surgery, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Keith F FournierDepartment of Surgical Oncology, Division of Surgery, University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Beth A HelminkDepartment of Surgical Oncology, Division of Surgery, University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
TRAINING OF ACADEMIC SURGICAL ONCOLOGISTST32CA009599 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Ashley M Holder, Jennifer A. Wargo · 1988 to 2026
$13.2M
Project 3: Inhibiting Oxidative Phosphorylation in Pancreatic CancerP50CA221707 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KOPETZ, SCOTT, MAITRA, ANIRBAN · 2019 to 2023
$11.0M
CTSA K12 Program at The University of Texas Health Science Center at HoustonK12TR004908 · NCATS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Charles C Miller, JON E. TYSON · 2024 to 2026
$2.9M
NCATS NIH HHS K12 TR004908NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA221707NCI NIH HHS T32 CA009599
6 · The paper itself

Abstract

Introduction: While cytoreductive surgery and hyperthermic intraperitoneal chemotherapy (CRS/HIPEC) can improve overall survival (OS) for patients with peritoneal carcinomatosis from appendiceal or colorectal cancer, some patients are ineligible for CRS/HIPEC due to disease burden. This paper characterizes outcomes for patients who are evaluated by diagnostic laparoscopy (DL) and deemed ineligible for CRS/HIPEC. Methods: Medical records were retrospectively reviewed for patients who underwent DL and deemed ineligible for CRS/HIPEC (1/1/2009-1/1/2024). Date of death was confirmed using public obituaries. Treatment course/causes of death are summarized by descriptive statistics and OS by Kaplan-Meier analysis. Results: 124 patients were included. Median Peritoneal Cancer Index (PCI) score was 25. Median follow-up was 1.14 and median OS 1.29 years. 58 (46.8 %) died of their malignancy, 42 (33.9 %) died of unknown cause, and 24 (19.4 %) were alive at last follow-up. The most common causes of death were bowel obstruction (29, 23.4 %), multifactorial/failure to thrive (21, 16.9 %), and malignant ascites (15, 12.1 %). Patients who underwent some form of additional therapy after DL (1.43 versus 0.48 years, p < 0.001) or who enrolled in a clinical trial (1.91 versus 1.21 years, p = 0.030) had prolonged OS. Conclusions: OS for patients with peritoneal carcinomatosis from appendiceal or colorectal cancer who are deemed ineligible for CRS/HIPEC after DL is 1.29 years without significant variation by primary pathology, PCI, peritoneal cytology, or presence of hematogenous metastases. Patients who get some form of additional therapy following their DL have prolonged OS. The most common causes of death are bowel obstruction, failure to thrive, and malignant ascites.

Indexed as

CRS-HIPECDiagnostic LaparoscopyPeritoneal

Identifiers

PMID40740309
PMCPMC12308341

What OpenQuestion holds

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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 OpenQuestion graph.