Evidence map›Paper›PMID 42082871›Full record

ArticleAnnals of surgical oncology2026

Neoadjuvant Therapy as a Selection Strategy for Curative Resection in High-Risk Intrahepatic Cholangiocarcinoma.

Yawen Dong, Kever A Lewis, David Pereyra, Zhihao Li, Vanja Podrascanin, Galen C Gist, Jonas Santol, Markus Ammann, Lionel A Kankeu Fonkoua, Rondell P Graham and 8 more

Abstract read
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In one paragraph

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. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Yawen DongDivision of Hepatobiliary and Pancreas Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, USA.
Kever A LewisDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
David PereyraDivision of Hepatobiliary and Pancreas Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, USA.
Zhihao LiDivision of Hepatobiliary and Pancreas Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, USA.
Vanja PodrascaninDivision of Hepatobiliary and Pancreas Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, USA.
Galen C GistDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jonas SantolDivision of Hepatobiliary and Pancreas Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, USA.
Markus AmmannDivision of Hepatobiliary and Pancreas Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, USA.
Lionel A Kankeu FonkouaDepartment of Medical Oncology, Mayo Clinic, Rochester, MN, USA.
Rondell P GrahamDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
Caitlin B ConboyDepartment of Medical Oncology, Mayo Clinic, Rochester, MN, USA.
Nguyen H TranDepartment of Medical Oncology, Mayo Clinic, Rochester, MN, USA.
Susanne G WarnerDivision of Hepatobiliary and Pancreas Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, USA.
Jean-Nicolas VautheyDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Timothy E NewhookDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Hop S Tran CaoDepartment of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Rory L SmootDivision of Hepatobiliary and Pancreas Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, USA.
Patrick StarlingerDivision of Hepatobiliary and Pancreas Surgery, Department of Surgery, Mayo Clinic, Rochester, MN, USA. starlinger.patrick@mayo.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHigh-risk features (e.g., vascular invasion, lymph node involvement, multifocality, elevated carbohydrate antigen 19-9 [CA19-9], tumor size >5 cm) in intrahepatic cholangiocarcinoma (iCCA) are associated with poor prognosis, leading to increased use of neoadjuvant therapy (NAT).

methodsPatients (n = 425) treated in 2000-2024 at Mayo Clinic Rochester were categorized into four groups: (1) high-risk iCCA with NAT (chemotherapy- or chemoimmunotherapy-based regimens) followed by surgery, (2) high-risk iCCA with upfront resection, (3) low-risk iCCA with upfront resection, and (4) high-risk iCCA receiving NAT without surgery ("dropouts"). Outcomes included overall (OS) and recurrence-free survival (RFS). An external cohort of 203 iCCA patients from MD Anderson Cancer Center also was analyzed using identical criteria.

resultsOf 425 patients, 342 (80.5%) were at high risk and 83 (19.5%) were at low risk (all upfront resection). Among the high-risk patients, 172 (50.3%) received NAT and 96 (55.8%) underwent upfront resection, whereas 76 (44.2%) dropped out. The NAT regimens included doublet gemcitabine-cisplatin (GC, n = 56) and triplet chemo(immuno)therapy with gemcitabine-cisplatin-nab-paclitaxel (GAP, n = 30) or gemcitabine-cisplatin-durvalumab (GCD, n = 10). The NAT patients who proceeded to resection showed significantly longer OS than those who had upfront resection (68.6 vs. 34.9 months; p = 0.007), with no significant difference from low-risk patients (106.2 months, p = 0.132). Intensified regimens (GAP/GCD) yielded superior OS, whereas RFS did not significantly differ across groups. Comparable survival trends were observed in the external cohort.

conclusionNeoadjuvant therapy followed by curative-intent resection was associated with improved OS, reflecting selection of systemic therapy-responsive high-risk patients with more favorable tumor biology, achieving outcomes similar to those of low-risk groups. Conversely, 45% failed to proceed to surgery due to progression or clinical deterioration, experiencing OS comparable with palliative care.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBile Duct NeoplasmsCholangiocarcinomaHepatectomyNeoadjuvant TherapyNeoplasm Recurrence, LocalAgedCombined Modality TherapyFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisRetrospective StudiesSurvival Rate

Identifiers

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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.