Evidence map›Paper›PMID 42430699›Full record

Observational studyJCO precision oncology2026

Long-Term Outcomes and Surgical Conversion After Immunotherapy in Microsatellite Instability-H Biliary Tract Cancers.

Priyanshi Shah, Anina Peersen, Vaibhav Sahai, Amit Mahipal, Nikolas Naleid, Mitesh Borad, Tanios Bekaii-Saab, Mohamad Bassam Sonbol, Umair Majeed, Hani M Babiker and 20 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in JCO precision 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

30 authors.

Priyanshi ShahDepartment of Oncology, Mayo Clinic Rochester, MN.ORCID 0000-0002-1537-2726
Anina PeersenDivision of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN.
Vaibhav SahaiDivision of Hematology and Oncology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI.ORCID 0000-0003-1892-1548
Amit MahipalDepartment of Oncology, University Hospitals Seidman Cancer Center and Case Western Reserve University, Cleveland, OH.ORCID 0000-0002-1111-8333
Nikolas NaleidDepartment of Oncology, University Hospitals Seidman Cancer Center and Case Western Reserve University, Cleveland, OH.ORCID 0009-0005-3297-1041
Mitesh BoradDivision of Hematology/Oncology, Mayo Clinic, Phoenix, AZ.ORCID 0000-0003-2700-2658
Tanios Bekaii-SaabDivision of Hematology/Oncology, Mayo Clinic, Phoenix, AZ.ORCID 0000-0001-7721-1699
Mohamad Bassam SonbolDivision of Hematology/Oncology, Mayo Clinic, Phoenix, AZ.ORCID 0000-0002-6931-242X
Umair MajeedDivision of Hematology/Oncology, Mayo Clinic, Jacksonville, FL.ORCID 0000-0002-4225-7555
Hani M BabikerDivision of Hematology/Oncology, Mayo Clinic, Jacksonville, FL.ORCID 0000-0002-9368-6296
Conor D J O'DonnellDivision of Hematology/Oncology, Mayo Clinic, Jacksonville, FL.
Midhun MallaDivision of Hematology and Oncology, University of Alabama, Birmingham, AL.ORCID 0000-0002-9969-588X
Garima GuptaDivision of Hematology and Oncology, University of Alabama, Birmingham, AL.
Caitlyn B ConboyDepartment of Oncology, Mayo Clinic Rochester, MN.ORCID 0000-0001-8280-056X
Lionel Kankeu FonkouaDepartment of Oncology, Mayo Clinic Rochester, MN.
Leslie A WashburnDepartment of Oncology, Mayo Clinic Rochester, MN.ORCID 0009-0003-3899-1831
Thorvardur R HalfdanarsonDepartment of Oncology, Mayo Clinic Rochester, MN.ORCID 0000-0001-8460-1257
Nicole PetersonDivision of Hematology and Oncology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI.ORCID 0009-0000-6035-4124
Robert R McWilliamsDepartment of Medical Oncology, OSF Healthcare Cancer Institute, Peoria, IL.ORCID 0000-0002-8199-5040
Ryan M CarrDepartment of Oncology, Mayo Clinic Rochester, MN.
Rondell P GrahamDepartment of Pathology, Mayo Clinic, Rochester, MN.ORCID 0000-0002-8686-4867
Patrick StarlingerDepartment of Surgery, Mayo Clinic, Rochester, MN.
Rory SmootDepartment of Surgery, Mayo Clinic, Rochester, MN.
Susanne WarnerDepartment of Surgery, Mayo Clinic, Rochester, MN.
Sumera I IlyasDepartment of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.
Gregory J GoresDepartment of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.ORCID 0000-0003-3151-009X
Lewis RobertsDepartment of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN.ORCID 0000-0001-7885-8574
Julie HeimbachDepartment of Transplant Surgery, Mayo Clinic, Rochester, MN.
Fang-Shu OuDivision of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN.ORCID 0000-0003-1267-8735
Nguyen H TranDepartment of Oncology, Mayo Clinic Rochester, MN.ORCID 0000-0002-6104-6489

Funding

Working to Eliminate Care Disparities in Liver Cancer in Southeast Asian Americans: Transportation and Other Social Determinants of Health.K23MD017217 · NIMHD · MAYO CLINIC ROCHESTER · PI Nguyen H Tran · 2022 to 2026
$818k
NIMHD NIH HHS K23 MD017217
6 · The paper itself

Abstract

purposeDeficient mismatch repair/microsatellite instability (dMMR, MSI-H) in biliary tract cancers (BTCs) is observed in 1%-5% of tumors. MSI-H across solid tumors has demonstrated durable response to immune checkpoint inhibitors (ICIs) regardless of the anatomic location. Here, we describe clinical outcomes and surgical conversion of MSI-H BTC treated with ICIs. PATIENTS AND

methodsWe conducted a multicenter, retrospective analysis of BTC patients with dMMR/MSI-H between 2017 and 2024 at Mayo Clinic, University of Michigan, and University Hospitals Seidman Cancer Center. Outcomes of interest were surgical resection rate, rate of pathologic response, 2-year overall survival (OS; time from initiation of treatment to death/last follow-up), and time to treatment discontinuation (TTD; time from initiation of treatment to cessation because of any cause). Analyses were descriptive.

resultsThirty patients with MSI-H BTC were identified: 19 with cholangiocarcinoma, three with gallbladder cancer, and 8 with BTC undefined. The median age at diagnosis was 61.5 years (range, 26-86). Twenty-six (86.7%) patients had advanced stage at diagnosis. Twenty-seven patients (90%) received first-line systemic therapy, and 13 (48.1%) continued onto second line. Six patients (23.1%) were restaged to resectable from advanced disease after ICI therapy and underwent resection; all remained recurrence-free at last follow-up. Of these six patients, 3 (50%) achieved a pathologic complete response. Among those receiving first-line therapy, the median TTD was 9.9 months (95% CI, 5.7 to 14.5 months) and the 2-year OS was 73% (95% CI, 56% to 94%).

conclusionICI therapy in patients with MSI-H BTC demonstrated durable response and downstaged some BTC to a resectable stage. dMMR/MSI-H should be performed up-front to guide treatment decisions.

Indexed as

Biliary Tract NeoplasmsImmunotherapyMicrosatellite InstabilityAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment Outcome

Identifiers

PMID42430699
PMCPMC13374654

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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.