Evidence map›Paper›PMID 42005101›Full record

ArticleCureus2026

An Uncommon Presentation of Selpercatinib (Retevmo)-Induced Severe Transaminitis: A Biopsy-Proven Case Report.

Navanita Biswas, Krishi Dudhia

Abstract readCase Reports
In one paragraph

Article in Cureus, 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

2 authors.

Navanita BiswasInternal Medicine, Tower Health Reading Hospital, Reading, USA.
Krishi DudhiaMedicine, Drexel University College of Medicine, Philadelphia, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Selpercatinib (Retevmo) is a selective rearranged during transfection (RET) kinase inhibitor approved for RET-altered malignancies, including thyroid carcinoma. Hepatic enzyme elevations have been reported; however, biopsy-proven drug-induced liver injury (DILI) associated with selpercatinib is uncommon. We report a case of a 59-year-old woman with recurrent papillary thyroid carcinoma who developed progressive gastrointestinal symptoms followed by severe hepatocellular transaminitis approximately four weeks after initiating selpercatinib (160 mg twice daily). Laboratory evaluation demonstrated marked aminotransferase elevation (aspartate aminotransferase: 525 U/L and alanine aminotransferase: 639 U/L) with mild hyperbilirubinemia (total bilirubin: 2.1 mg/dL), and aminotransferases peaked above 800 U/L during hospitalization. Comprehensive workup for alternative etiologies, including viral hepatitis and autoimmune hepatitis (negative antinuclear antibody and smooth muscle antibody with normal immunoglobulin levels), was unrevealing, and abdominal imaging showed no acute abnormalities. Liver biopsy demonstrated sparse portal lymphocytic inflammation with intact bile ducts and prominent centrilobular (zone 3) hepatocellular necrosis accompanied by macrophages and eosinophils, consistent with DILI. Selpercatinib was discontinued, resulting in progressive biochemical improvement with aminotransferases declining to <100 U/L within approximately four months. Given oncologic necessity, selpercatinib was reintroduced at a reduced dose (40 mg daily) without recurrence of severe transaminitis. This case highlights that selpercatinib can cause clinically significant hepatocellular DILI and underscores the diagnostic value of liver biopsy in distinguishing DILI from autoimmune hepatitis, particularly when considering safe dose modification and rechallenge.

Indexed as

drug-induced hepatotoxicity (dih)liver biopsyretevmoret inhibitorselpercatinib

Identifiers

PMID42005101
PMCPMC13085463

What Socratic holds

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Registered trials

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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 Socratic graph.