Evidence map›Paper›PMID 35802197›Full record

ArticleJournal of cancer research and clinical oncology2023

Triple therapy in biliary tract cancers: GemOX plus immune checkpoint inhibitor in combination with lenvatinib or NGS-guided targeted therapy.

Xiang Dong, Zewu Zhang, Qin Zhang, Lu Chen, Guangtai Cao, Chen Liu, Tianqiang Song, Wei Lu, Wei Zhang

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% of its field
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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
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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

9 authors at 2 institutions in 1 country.

Xiang Dong *Department of Hepatobiliary Cancer, Research Center for Prevention and Treatment of Liver Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital. National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Huan Hu Xi Road, Tianjin, 300060, China.
Zewu Zhang *Department of Hepatobiliary Cancer, Research Center for Prevention and Treatment of Liver Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital. National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Huan Hu Xi Road, Tianjin, 300060, China.
Qin Zhang *Department of Hepatobiliary Cancer, Research Center for Prevention and Treatment of Liver Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital. National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Huan Hu Xi Road, Tianjin, 300060, China.
Lu ChenDepartment of Hepatobiliary Cancer, Research Center for Prevention and Treatment of Liver Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital. National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Huan Hu Xi Road, Tianjin, 300060, China.
Guangtai CaoDepartment of General Surgery, Cangzhou Hospital of Integrated Traditional Chinese and Western Medicine, Cangzhou, Hebei, China.
Chen LiuDepartment of Hepatobiliary Cancer, Research Center for Prevention and Treatment of Liver Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital. National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Huan Hu Xi Road, Tianjin, 300060, China.
Tianqiang SongDepartment of Hepatobiliary Cancer, Research Center for Prevention and Treatment of Liver Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital. National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Huan Hu Xi Road, Tianjin, 300060, China.
Wei LuDepartment of Hepatobiliary Cancer, Research Center for Prevention and Treatment of Liver Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital. National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Huan Hu Xi Road, Tianjin, 300060, China.
Wei ZhangDepartment of Hepatobiliary Cancer, Research Center for Prevention and Treatment of Liver Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin Medical University Cancer Institute and Hospital. National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Huan Hu Xi Road, Tianjin, 300060, China. zhangweitjch@163.com.ORCID http://orcid.org/0000-0002-2439-6076
Tianjin Medical University Cancer Institute and Hospital · CNPeople's Hospital of Cangzhou · CN

Funding

Tianjin Medical University Cancer Institute and Hospital 2021-014
6 · The paper itself

Abstract

purposeThe combination of gemcitabine-based chemotherapy and immune checkpoint inhibitors has a good efficacy in advanced biliary tract cancer (BTC). The multi-target TKI lenvatinib and NGS-guided targeted therapy are also promising in BTC treatment. This study aimed to explore the performance of GemOX plus sintilimab and TKI (either lenvatinib or by NGS-guided targeted therapy) for local advanced or metastatic BTCs.

methodsThis prospective single-arm study included patients with local advanced or metastatic BTCs and applied intravenous infusion of standard GemOX plus sintilimab and lenvatinib (no targetable gene alterations) or targeted therapy based on NGS (olaparib for BRCA1/2 mutation, dasatinib for IDH1/2 mutation, afatinib for EGFR amplification, lenvatinib for PDGFR and KIT mutation, and lenvatinib for FGFR/KIT mutation).

resultsFrom November 2020 to December 2021, 22 patients BTCs (6 GBC, 14 iCCA, 1 pCCA and 1 dCCA cases) were enrolled, with an average age of 58.4 years. Partial response (PR) was achieved in 10 cases, stable disease (SD) in 9 cases and progression disease (PD) in 3 cases (13.6%). The objective response rate (ORR) was 45.5%, and the disease control rate (DCR) was 86.4%. During the treatment, the incidence of adverse reactions was 81.8%, and the incidence of grade 3/4 adverse events was 9.09%. For 14 patients with NGS, 5 patients were treated by targeted therapy and there were 1 SD and 4 PR cases. For four patients with positive PD-L1 expression, the ORR was 100%. While among the three patients with super-progression markers such as RET, MDM2 and FGF14/STK24, there were two SD and one PD cases.

conclusionIn patients with advanced BTCs, the combination of GemOX plus sintilimab and lenvatinib or NGS-guided targeted therapy showed promising ORR and DCR, especially for the patients with positive PD-L1 expression and targetable gene alterations.

Indexed as

Biliary Tract NeoplasmsImmune Checkpoint InhibitorsAntineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenDeoxycytidineHumansMiddle AgedOxaliplatinPhenylurea CompoundsProspective StudiesQuinolinesB7-H1 AntigenDeoxycytidineImmune Checkpoint InhibitorslenvatinibOxaliplatinPhenylurea CompoundsQuinolinesBiliary tract cancerImmunotherapyNext-generation sequencingPD-L1Targeted therapy

Identifiers

PMID35802197
PMCPMC11797449
OpenAlexW4284962032

What OpenQuestion holds

Textmetadata
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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.