Evidence map›Paper›PMID 42620227›Full record

ArticleFrontiers in oncology2026

Risk factors for irinotecan-induced hepatotoxicity: a retrospective cohort study.

Fatemah A Alherz, Anwar M Alnakhli, Aisha M Alqarni, Alanoud F Alshammari, Alhanouf M Ruwayi, Rahaf M Alyamani, Haya Al-Salloum, Mohammad J Al-Yamani, Farag Shuweihdi

Abstract read
In one paragraph

Article in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Fatemah A AlherzDepartment of Pharmaceutical Sciences, College of Pharmacy, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
Anwar M AlnakhliDepartment of Pharmaceutical Sciences, College of Pharmacy, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
Aisha M AlqarniCollege of Pharmacy, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
Alanoud F AlshammariCollege of Pharmacy, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
Alhanouf M RuwayiCollege of Pharmacy, Princess Nourah bint Abdulrahman University, Riyadh, Saudi Arabia.
Rahaf M AlyamaniCollege of Medicine, Almaarefa University, Riyadh, Saudi Arabia.
Haya Al-SalloumDepartment of Pharmacy Services, King Saud University Medical City, Riyadh, Saudi Arabia.
Mohammad J Al-YamaniDepartment of Pharmacy Practice, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.
Farag ShuweihdiSchool of Dentistry, University of Leeds, Leeds, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Irinotecan is a potent chemotherapeutic agent used as a neoadjuvant in colorectal cancer liver metastasis and significantly enhances five-year survival rates. Recently, irinotecan-associated hepatotoxicity was a significant concern. Given the limited study in this area, we aimed to identify risk factors associated with irinotecan-induced hepatotoxicity. Methods: This is a retrospective cohort study at King Saud University Medical City in Riyadh. The study encompassed all adult cancer patients who received irinotecan treatment between Jun 2017 and December 2023. The clinical records of patients were reviewed to assess factors associated with hepatotoxicity. Time-to-event analyses were performed using time-varying exposure. Results: The study includes 229 adult cancer patients who received irinotecan-based treatment. Median age was 58 years, and colorectal cancer was the most diagnosed type of cancer (68.6%). Over a median follow-up of 103 days, the incidence of hepatotoxicity was 19.2% (n=44). In the adjusted analysis, higher baseline AST was associated with an increased hazard of hepatotoxicity (HR = 1.01; 95% CI: 1.01-1.02; Conclusion: In summary, an inverse association was observed between cumulative irinotecan dose and hepatotoxicity. A higher baseline AST was also associated with hepatotoxicity, warranting careful assessment of pretreatment liver enzymes and closer monitoring during the early treatment period. Further studies are needed to validate these findings and investigate additional predictors of irinotecan-related hepatotoxicity.

Indexed as

colorectal cancerhepatotoxicityirinotecanirinotecan-induced hepatotoxicityliver enzymesliver function tests

Identifiers

PMID42620227
PMCPMC13485589

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.