Evidence map›Paper›PMID 41032264›Full record

ArticleThe oncologist2025

Lenvatinib after progression on pemigatinib and futibatinib in FGFR2 fusion-positive biliary tract cancer with an acquired kinase point mutation.

Fabian Kleinhenz, Nicole Pfarr, Lisa Steinhelfer, Alisa M Lörsch, Henriette Bendz, Mathias Friedrich, Lea Liesenfeld, Melissa Barroux, Carlo Maurer, Patrick Wenzel and 8 more

Abstract readCase Reports
In one paragraph

Article in The oncologist, 2025. 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

18 authors.

Fabian KleinhenzClinical Department of Internal Medicine II, TUM School of Medicine and Health, TUM University Hospital, Munich 81675, Germany.
Nicole PfarrInstitute of Pathology, TUM School of Medicine and Health, Technical University of Munich, Munich 81675, Germany.ORCID 0000-0002-5977-5375
Lisa SteinhelferDepartment of Radiology, TUM School of Medicine and Health, TUM University Hospital, Munich 81675, Germany.
Alisa M LörschCenter for Personalized Medicine, TUM School of Medicine and Health, TUM University Hospital, Munich 81675, Germany.
Henriette BendzClinical Department of Internal Medicine II, TUM School of Medicine and Health, TUM University Hospital, Munich 81675, Germany.
Mathias FriedrichClinical Department of Internal Medicine II, TUM School of Medicine and Health, TUM University Hospital, Munich 81675, Germany.
Lea LiesenfeldClinical Department of Internal Medicine II, TUM School of Medicine and Health, TUM University Hospital, Munich 81675, Germany.
Melissa BarrouxClinical Department of Internal Medicine II, TUM School of Medicine and Health, TUM University Hospital, Munich 81675, Germany.
Carlo MaurerClinical Department of Internal Medicine II, TUM School of Medicine and Health, TUM University Hospital, Munich 81675, Germany.
Patrick WenzelClinical Department of Internal Medicine II, TUM School of Medicine and Health, TUM University Hospital, Munich 81675, Germany.
Angelika KestlerDepartment of Internal Medicine I, University Hospital Ulm, Ulm 89081, Germany.
Mai-Lan KoppermannInstitute of Pathology, TUM School of Medicine and Health, Technical University of Munich, Munich 81675, Germany.
Carolin MoglerInstitute of Pathology, TUM School of Medicine and Health, Technical University of Munich, Munich 81675, Germany.
Stephan SpahnDepartment of Internal Medicine I, University Hospital, Eberhard-Karls University, 72076 Tuebingen, Germany.
Anna L IllertCenter for Personalized Medicine, TUM School of Medicine and Health, TUM University Hospital, Munich 81675, Germany.
Roland M SchmidClinical Department of Internal Medicine II, TUM School of Medicine and Health, TUM University Hospital, Munich 81675, Germany.
Michael BitzerDepartment of Internal Medicine I, University Hospital, Eberhard-Karls University, 72076 Tuebingen, Germany.
Sebastian LangeClinical Department of Internal Medicine II, TUM School of Medicine and Health, TUM University Hospital, Munich 81675, Germany.ORCID 0000-0003-0406-1401

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biliary tract cancers (BTC) represent a heterogeneous group of malignancies with a poor prognosis and rising incidence. Oncogenic FGFR2 fusions are one of several actionable molecular alterations. In this context, selective FGFR tyrosine kinase inhibitors have demonstrated promising and durable response rates and are now approved and included in clinical guidelines. However, secondary kinase mutations frequently arise over time, leading to resistance against these drugs. We present the case of a 41-year-old male patient with metastatic BTC who underwent molecular analysis after disease progression to various established chemotherapy combinations. Testing identified an oncogenic FGFR2 fusion (FGFR2::BICC1). The patient was treated with pemigatinib for 14 months. Upon disease progression, the resistance-associated FGFR2 p. E565A variant was detected in a follow-up biopsy. Treatment was switched to futibatinib, resulting in rapid disease progression. Lacking other therapeutic options, the patient was treated with lenvatinib, supported by previously published data suggesting a potential benefit in similar settings. The treatment was well tolerated, with only a mild increase in transaminases, and the patient remained on treatment with noteworthy effects for 15 months to date. With a growing incidence of BTC and growing use of targeted therapies for FGFR2 alterations, the emergence of secondary resistance-causing point mutations following treatment with approved inhibitors is becoming increasingly challenging. Beyond selective inhibitors, lenvatinib may represent a viable therapeutic option.

Indexed as

Biliary Tract NeoplasmsPhenylurea CompoundsPyridazinesPyrimidinesQuinolinesReceptor, Fibroblast Growth Factor, Type 2AdultDisease ProgressionHumansMaleMorpholinesOncogene Proteins, FusionPoint MutationProtein Kinase InhibitorsPyrrolesFGFR2 protein, humanlenvatinibMorpholinesOncogene Proteins, FusionpemigatinibPhenylurea CompoundsProtein Kinase InhibitorsPyridazinesPyrimidinesPyrrolesQuinolinesReceptor, Fibroblast Growth Factor, Type 2BTCCCAFGFR2-fusion geneFGFR alterationLenvatinibTKIs

Identifiers

PMID41032264
PMCPMC12557317

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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.