Evidence map›Paper›PMID 32602010›Full record

ReviewCurrent treatment options in oncology2020

New Treatment Options for Advanced Biliary Tract Cancer.

Jonathan D Mizrahi, Rachna T Shroff

2 registry-linked trialsAbstract readReview
PubMed Publisher
In one paragraph

Review in Current treatment options in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 3% 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.

NCT06739252 phase2terminatednot on this mapstarted 2024, after this paper: background citation

Perioperative Treatment of High-risk Resectable Cholangiocarcinoma With Hepatic Arterial Infusion Chemotherapy (HAIC) Combined With Atezo/Bevacizumab: a Multicenter Phase II Study (NeoBrave CCA)

TypeinterventionalSponsorPeking UniversityRan2024 to 2025Enrolled1ConditionsIntrahepatic Cholangiocarcinoma (Icc), Perihilar CholangiocarcinomaArmsGemcitabine Oxaliplatin and 5FU
NCT07156058 narecruitingnot on this mapstarted 2023, after this paper: background citation

MiniPDX-based Postoperative Adjuvant Therapy for Biliary Tract Cancer: A Prospective Cohort Study

TypeinterventionalSponsorCancer Institute and Hospital, Chinese Academy of Medical SciencesRan2023 to 2025Enrolled204ConditionsBiliary Tract CancerArmsMiniPDX group, Capecitabine
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

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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

2 authors at 2 institutions in 1 country.

Jonathan D MizrahiThe University of Texas MD Anderson Cancer Center, 1400 Holcombe Blvd Unit 463, Houston, TX, 77030, USA. jdmizrahi@mdanderson.org.
Rachna T ShroffUniversity of Arizona Cancer Center, 1400 Holcombe Blvd Unit 463, Tucson, AZ, 77030, USA. rshroff@email.arizona.edu.
The University of Texas MD Anderson Cancer Center · USUniversity of Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

opinion statementThe standard of care first-line therapy for patients with advanced biliary tract cancers eligible for treatment continues to be the combination of gemcitabine and cisplatin. Based on the promising results of a phase II study, an ongoing multi-institutional phase III study is assessing the benefit of adding nab-paclitaxel to the chemotherapy doublet, and appropriate patients should be considered for enrollment at participating centers. We would recommend early comprehensive genomic profiling of patients' tumors to identify potentially targetable aberrations with available therapies. Results with therapeutic implications include tumors with microsatellite instability/deficient mismatch repair, alterations in FGFR, IDH1/2, and HER-2, and potentially other molecular vulnerabilities. Patients in whom a targetable genomic abnormality is found should be matched with appropriate agent. If a targetable fusion or mutation is not detected, patients eligible for second-line therapy should be considered for either clinical trial enrollment or a second-line cytotoxic chemotherapy regimen such as modified FOLFOX. Strategies incorporating immunotherapy into the treatment of patients with microsatellite stable advanced biliary tract cancers have yielded largely disappointing results thus far, and routine use of checkpoint inhibitors outside of a clinical trial is not recommended.

Indexed as

Biliary Tract NeoplasmsBiomarkers, TumorClinical Decision-MakingCombined Modality TherapyDisease ManagementDisease SusceptibilityGenetic Predisposition to DiseaseHumansNeoplasm MetastasisNeoplasm StagingTreatment OutcomeBiomarkers, TumorBiliary tract cancerCholangiocarcinomaGall bladder cancerImmunotherapyTargeted therapy

Identifiers

PMID32602010
OpenAlexW3038549225

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.