Evidence map›Paper›PMID 42426481›Full record

ArticleAnnals of surgical oncology2026

Investigating Age-Related Differences in Survival Outcomes and Mutation Status of Patients with Intrahepatic Cholangiocarcinoma.

Misha Armstrong, Hannah Kalvin, Mithat Gönen, Ghassan Abou-Alfa, Vinod P Balachandran, Andrea Cercek, Michael I D'Angelica, James Harding, T Peter Kingham, Eileen O'Reilly and 3 more

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Article in Annals of surgical 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.

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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

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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

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Misha ArmstrongHepatopancreatobiliary Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Hannah KalvinDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Mithat GönenDepartment of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Ghassan Abou-AlfaDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Vinod P BalachandranHepatopancreatobiliary Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Andrea CercekDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Michael I D'AngelicaHepatopancreatobiliary Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
James HardingDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
T Peter KinghamHepatopancreatobiliary Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Eileen O'ReillyDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Kevin C SoaresHepatopancreatobiliary Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Alice C WeiHepatopancreatobiliary Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
William JarnaginHepatopancreatobiliary Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA. jarnagiw@mskcc.org.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundSurvival outcomes for intrahepatic cholangiocarcinoma (IHC) remain poor due to late-stage presentation and limited effective treatment options. Previous studies have suggested age-related differences in outcome, but the results are mixed, and there is substantial variation in the definition of "young."

methodsA retrospective review analyzed 938 consecutive patients with a diagnosis of IHC between 2000 and 2018 at a single institution. Risk factors for IHC, clinical characteristics at diagnosis, and genomics were assessed for potential differences at the extremes of age (≤50 vs ≥70 years).

resultsThe final cohort (n = 430) included 142 patients 50 years or younger and 288 patients older than 70. The most common genetic alterations were IDH1mut (22%), p53mut (17%), KRASmut (9.8%), and FGFR2fus (6.3%). Young patients had a higher proportion of FGFR2fus (p = 0.020). The median overall survival (OS) for the entire cohort was 23 months (95% confidence interval [CI], 20-27 months). In the resected group, recurrence-free survival (RFS) was longer for the older patients (median 27 vs 17months), but OS did not differ significantly (23 vs 25 months; p = 0.3). By contrast, among the unresectable patients, OS was significantly better for the younger patients (p = 0.008), but no significant relationship was observed between age and resection status when OS was assessed (p = 0.7).

conclusionGenomic differences between older and younger patients did not appear to drive the differences in OS observed in this cohort. Intrahepatic cholangiocarcinoma patients 50 years or younger likely do not represent a distinct subgroup despite differences in presentation and clinical characteristics.

Indexed as

Bile Duct NeoplasmsBiomarkers, TumorCholangiocarcinomaMutationAdultAgedAged, 80 and overAge FactorsFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisProto-Oncogene Proteins p21(ras)Receptor, Fibroblast Growth Factor, Type 2Biomarkers, TumorFGFR2 protein, humanKRAS protein, humanProto-Oncogene Proteins p21(ras)Receptor, Fibroblast Growth Factor, Type 2Age-related differencesCholangiocarcinomaFGFR2KRASMutationSurvival outcomes

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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.