Evidence map›Paper›PMID 35310729›Full record

ArticleDEN open2022

Endoscopic and histopathologic features of Anti-PD-1-related collagenous colitis.

Hidezumi Kikuchi, Hirotake Sakuraba, Yui Akemoto, Kazuhiro Hosoi, Yasuhisa Murai, Kentaro Hoshi, Yukari Fukutoku, Taka Asari, Yohei Sawada, Keisuke Hasui and 5 more

Open access · goldAbstract read
In one paragraph

Article in DEN open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. Collagenous colitis associated with novel sprue-like intestinal diseases.Gastroenterology and hepatology from bed to bench · 2023
    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

15 authors at 2 institutions in 1 country.

Hidezumi KikuchiDepartment of Gastroenterology and Hematology Hirosaki University Graduate School of Medicine Aomori Japan.ORCID https://orcid.org/0000-0002-5163-9563
Hirotake SakurabaDepartment of Gastroenterology and Hematology Hirosaki University Graduate School of Medicine Aomori Japan.
Yui AkemotoDepartment of Anatomic Pathology Hirosaki University Hospital Aomori Japan.
Kazuhiro HosoiDepartment of Pharmacy Hirosaki University Hospital Aomori Japan.
Yasuhisa MuraiDepartment of Gastroenterology and Hematology Hirosaki University Graduate School of Medicine Aomori Japan.ORCID https://orcid.org/0000-0002-3305-1248
Kentaro HoshiDepartment of Gastroenterology and Hematology Hirosaki University Graduate School of Medicine Aomori Japan.
Yukari FukutokuDepartment of Gastroenterology and Hematology Hirosaki University Graduate School of Medicine Aomori Japan.
Taka AsariDepartment of Gastroenterology and Hematology Hirosaki University Graduate School of Medicine Aomori Japan.
Yohei SawadaDepartment of Gastroenterology and Hematology Hirosaki University Graduate School of Medicine Aomori Japan.
Keisuke HasuiDepartment of Gastroenterology and Hematology Hirosaki University Graduate School of Medicine Aomori Japan.
Tetsuya TatsutaDepartment of Gastroenterology and Hematology Hirosaki University Graduate School of Medicine Aomori Japan.
Hiroto HiragaDepartment of Gastroenterology and Hematology Hirosaki University Graduate School of Medicine Aomori Japan.
Daisuke ChindaDepartment of Gastroenterology and Hematology Hirosaki University Graduate School of Medicine Aomori Japan.ORCID https://orcid.org/0000-0003-1690-5923
Tatsuya MikamiInnovation Center for Health Promotion Hirosaki University Graduate School of Medicine Aomori Japan.
Shinsaku FukudaDepartment of Gastroenterology and Hematology Hirosaki University Graduate School of Medicine Aomori Japan.
Hirosaki University · JPHirosaki University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Cancer patients treated with immune checkpoint inhibitors occasionally show persistent diarrhea accompanied by endoscopic features of ulcerative colitis. The endoscopic mucosal inflammation may appear mild in some patients compared to the clinical severity, which can make choosing a treatment challenging. In this study, we evaluated the factors that support the continuation of chemotherapy by assessing the endoscopic and histopathological characteristics of patients who experienced diarrhea after immune checkpoint inhibitor administration. Methods: This study included eight patients who were diagnosed with collagenous colitis based on pathological assessments. We retrospectively investigated these patients' backgrounds, laboratory data, and computed tomography images that were extracted from their medical records. We also summarized their endoscopic and pathologic findings. Results: All eight patients were being treated with anti-programmed cell death-1/programmed cell death-ligand 1 therapeutic agents and had a recent history of oral proton pump inhibitor therapy. The anti-programmed cell death-1-related collagenous colitis in these cases was characterized by endoscopically mild mucosal inflammation, high fecal calprotectin levels, and a lower frequency of intestinal wall thickening on computed tomography. Histological assessments showed CD8 Conclusions: Anti-programmed cell death-1-related collagenous colitis is reversible; appropriate diagnosis of adverse events is crucial for the continuation of immune checkpoint inhibitor therapy.

Indexed as

CD8‐positive T‐lymphocytescollagenous colitisdiarrheaimmune checkpoint inhibitorproton pump inhibitor

Identifiers

PMID35310729
PMCPMC8828179
OpenAlexW4206124247

What OpenQuestion holds

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LicenceCC BY
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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.