Evidence map›Paper›PMID 32638367›Full record

Trial reportThe British journal of surgery2020

Phase I/II study of adding intraperitoneal paclitaxel in patients with pancreatic cancer and peritoneal metastasis.

S Yamada, T Fujii, T Yamamoto, H Takami, I Yoshioka, S Yamaki, F Sonohara, K Shibuya, F Motoi, S Hirano and 9 more

Open access · hybridAbstract readClinical Trial, Phase IClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in The British journal of surgery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 2 pooled it
3.4field-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.

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

28 citing papers in PubMed, 2 syntheses or guidelines pooled it, 57 citations in OpenAlex.

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  12. A Case of Successful Conversion Surgery forSurgical case reports · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 10 institutions in 1 country.

S YamadaGastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID 0000-0001-9912-9119
T FujiiDepartment of Surgery and Science Faculty of Medicine, Academic Assembly, University of Toyama, Toyama, Japan.
T YamamotoDepartment of Surgery, Kansai Medical University, Hirakata, Japan.ORCID 0000-0002-7951-7429
H TakamiGastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
I YoshiokaDepartment of Surgery and Science Faculty of Medicine, Academic Assembly, University of Toyama, Toyama, Japan.
S YamakiDepartment of Surgery, Kansai Medical University, Hirakata, Japan.
F SonoharaGastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
K ShibuyaDepartment of Surgery and Science Faculty of Medicine, Academic Assembly, University of Toyama, Toyama, Japan.
F MotoiDepartment of Surgery, Tohoku University Graduate School of Medicine, Sendai, Japan.
S HiranoDepartment of Surgery, Institute of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Y MurakamiDepartment of Gastroenterological Surgery II, Faculty of Medicine, Hokkaido University, Sapporo, Japan.ORCID 0000-0001-6208-3081
H InoueDepartment of Hepatobiliary-pancreatic and Breast Surgery, Ehime University Graduate School of Medicine, Ehime, Fukuoka, Japan.
M HayashiGastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
K MurotaniBiostatistics Centre, Graduate School of Medicine, Kurume University, Fukuoka, Japan.
J KitayamaDepartment of Gastrointestinal Surgery, Jichi Medical University, Tochigi, Japan.
H IshikawaDepartment of Molecular-Targeting Cancer Prevention, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Y KoderaGastroenterological Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
M SekimotoDepartment of Surgery, Kansai Medical University, Hirakata, Japan.
S SatoiDepartment of Surgery, Kansai Medical University, Hirakata, Japan.ORCID 0000-0001-6527-5409
Nagoya University · JPKansai Medical University · JPUniversity of Toyama · JPEhime University · JPHiroshima University · JPHokkaido University · JPJichi Medical University · JPKurume University · JPKyoto Prefectural University of Medicine · JPTohoku University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntraperitoneal chemotherapy using paclitaxel is considered an experimental approach for treating peritoneal carcinomatosis. This study aimed to determine the recommended dose, and to evaluate the clinical efficacy and safety, of the combination of intravenous gemcitabine, intravenous nab-paclitaxel and intraperitoneal paclitaxel in patients with pancreatic cancer and peritoneal metastasis.

methodsThe frequencies of dose-limiting toxicities were evaluated, and the recommended dose was determined in phase I. The primary endpoint of the phase II analysis was overall survival rate at 1 year. Secondary endpoints were antitumour effects, symptom-relieving effects, safety and overall survival.

resultsThe recommended doses of intravenous gemcitabine, intravenous nab-paclitaxel and intraperitoneal paclitaxel were 800, 75 and 20 mg/m

conclusionAdding intraperitoneal paclitaxel had clinical efficacy with acceptable tolerability.

Indexed as

AgedAntineoplastic Agents, PhytogenicAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Pancreatic DuctalDose-Response Relationship, DrugFemaleFollow-Up StudiesHumansInjections, IntraperitonealLogistic ModelsMaleMiddle AgedPaclitaxelPancreatic NeoplasmsPeritoneal NeoplasmsSurvival AnalysisAntineoplastic Agents, PhytogenicPaclitaxel

Identifiers

PMID32638367
PMCPMC7689756
OpenAlexW3040038295

What OpenQuestion holds

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Registered trials

None linked

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.