Evidence map›Paper›PMID 41591448›Full record

ArticleCancer immunology, immunotherapy : CII2026

Local-regional therapy plus ICIs, chemotherapy, and lenvatinib versus ICIs plus chemotherapy in advanced intrahepatic cholangiocarcinoma: a multicenter study.

Mingming Wang, Shuofeng Li, Guanhua Yu, An Zhang, Shikang Ding, Yihong Zhang, Shi Feng, Zixiang Zhou, Mingjian Piao, Weixuan Pan and 9 more

Abstract readClinical StudyComparative StudyMulticenter Study
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 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

19 authors.

Mingming Wang *Department of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Shuofeng Li *Department of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Guanhua Yu *Department of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
An Zhang *National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Shikang Ding *Department of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Yihong ZhangDepartment of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Shi FengDepartment of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Zixiang ZhouDepartment of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Mingjian PiaoDepartment of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Weixuan PanDepartment of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Chengjie LiDepartment of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Boyu SunDepartment of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Jiongyuan LiDepartment of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Nan ZhangDepartment of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Xinyuan ChenDepartment of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. chenxinyuan_pumc@163.com.
Yongliang SunDepartment of Hepatobiliary and Pancreatic Surgery, China-Japan Friendship Hospital, Beijing, China. sunyongliang1982@hotmail.com.
Wen ZhangNational Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. wenwen0605@163.com.
Zhenyu ZhuDepartment of Hepatobiliary Surgery, The Fifth Medical Center of PLA General Hospital, Beijing, China. zhuzy302@163.com.
Haitao ZhaoDepartment of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China. zhaoht@pumch.cn.

Funding

CAMS Innovation Fund for Medical Sciences (CIFMS) 2021-I2M-1-061National High Level Hospital Clinical Research Funding 2022-PUMCH-B-128
6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) plus chemotherapy serve as the primary treatment for advanced intrahepatic cholangiocarcinoma (ICC), but they present limited effectiveness. This multicenter study intended to evaluate the feasibility of LRT plus ICIs, chemotherapy, and lenvatinib in patients with advanced ICC.

methodsPatients receiving LRT-ICIs-Chemotherapy-Lenvatinib (LRT-ICI-Chemo-Len group, N = 66) or ICIs-Chemotherapy (ICI-Chemo group, N = 81) between April 2020 and May 2025 were enrolled. The study's outcomes included progression-free survival (PFS), overall survival (OS), tumor response, and adverse events (AEs).

resultsThe LRT-ICI-Chemo-Len group showed notable enhancement in median PFS (9.9 months vs. 7.6 months, P = 0.004), median OS (20.9 months vs. 13.7 months, P = 0.004), objective response rate (ORR: 59.1% vs. 27.2%), and disease control rate (DCR: 93.9% vs. 84.0%). Conversion resection was performed in 8/66 (12.1%) in the LRT-ICI-Chemo-Len group, statistically higher than the 2.5% in the ICI-Chemo group. There was no statistically significant difference in the incidence of grade 3-4 AE between the LRT-ICI-Chemo-Len group (65.2%) and the ICI-Chemo group (56.8%) (P = 0.389). The most common grade 3-4 AE in the LRT-ICI-Chemo-Len group was myelosuppression. In the ICI-Chemo group, the most frequent grade 3-4 AE was myelosuppression. All AEs were manageable, with no grade 5 AE observed.

conclusionsCompared with the ICI-Chemo regimen, the LRT-ICI-Chemo-Len regimen significantly improved the prognosis of patients with advanced ICC. There was no significant difference in the incidence of grade 3-4 AEs between the two treatment regimens, and all AEs were manageable. This indicates that the LRT-ICI-Chemo-Len combination regimen is a feasible approach for the first-line treatment of advanced ICC.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBile Duct NeoplasmsCholangiocarcinomaImmune Checkpoint InhibitorsPhenylurea CompoundsQuinolinesAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedImmune Checkpoint InhibitorslenvatinibPhenylurea CompoundsQuinolinesChemotherapyImmunotherapyIntrahepatic cholangiocarcinomaLocal-regional therapyTargeted therapy

Identifiers

PMID41591448
PMCPMC12847575

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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 OpenQuestion graph.