Evidence map›Paper›PMID 29501212›Full record

ReviewCurrent problems in cancer

Immunotherapy as a treatment for biliary tract cancers: A review of approaches with an eye to the future.

Alex B Blair, Adrian Murphy

Open access · greenAbstract readReview
In one paragraph

Review in Current problems in cancer. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Observational
  9. Article
  10. Article
  11. Article
  12. Immunotherapy in Gastrointestinal Malignancies.Advances in experimental medicine and biology · 2021
    Article
  13. Oncology letters · 2020
    Article
  14. Review
  15. Review
  16. Article
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 1 institution in 1 country.

Alex B BlairDepartment of Surgery, Johns Hopkins Hospital, Baltimore, MD; Department of Oncology, The Sidney Kimmel Cancer Center, Johns Hopkins Hospital, Baltimore, MD.
Adrian MurphyDepartment of Oncology, The Sidney Kimmel Cancer Center, Johns Hopkins Hospital, Baltimore, MD. Electronic address: amurph39@jhmi.edu.
Sidney Kimmel Comprehensive Cancer Center · US

Funding

Tumor Antigens for Individual Signatures and TherapyP50CA062924 · NCI · JOHNS HOPKINS UNIVERSITY · PI LENNON, ANNE MARIE · 1993 to 2022
$54.6M
Clinical and Laboratory Research Training for Surgical OncologistsT32CA126607 · NCI · JOHNS HOPKINS UNIVERSITY · PI CAMERON, ANDREW M. · 2008 to 2024
$6.0M
NCI NIH HHS P50 CA062924NCI NIH HHS T32 CA126607
6 · The paper itself

Abstract

Biliary tract cancers (BTC) are aggressive malignancies associated with resistance to chemotherapy and poor prognostic rates. Therefore, novel treatment approaches are in need. Immunotherapy represents a promising breakthrough that uses a patient's immune system to target a tumor. This treatment approach has shown immense progress with positive results for selected cancers such as melanoma and nonsmall cell lung cancer. Initial preclinical data and preliminary clinical studies suggest encouraging mechanistic effects for immunotherapy in BTC offering the hope for an expanding therapeutic role for this disease. These approaches include targeted tumor antigen therapy via peptide and dendritic cell-based vaccines, allogenic cell adoptive immunotherapy, and the use of inhibitory agents targeting the immune checkpoint receptor pathway and multiple components of the tumor microenvironment. At this time demonstrating efficacy in larger clinical trials remains imperative. A multitude of ongoing trials aim to successfully translate mechanistic effects into antitumor efficacy and ultimately aim to incorporate immunotherapy into the routine management of BTC. With further research efforts, the optimization of dosing and therapeutic regimens, the identification of novel tumor antigens and a better understanding of alternative checkpoint pathway receptor expression may provide additional targets for rational combinatorial therapies which enhance the effects of immunotherapy and may offer hope for further advancing treatment options. Ultimately, the challenge remains to prospectively identify the subsets of patients with BTC who may respond to immunotherapy, and devising alternative strategies to sensitize those that do not with the hopes of improving outcomes for all with this deadly disease.

Indexed as

ImmunotherapyAntineoplastic Agents, ImmunologicalBiliary Tract NeoplasmsCancer VaccinesCell Cycle CheckpointsCholangiocarcinomaHumansImmunotherapy, AdoptiveMedical OncologyProtein Kinase InhibitorsT-LymphocytesAntineoplastic Agents, ImmunologicalCancer VaccinesProtein Kinase InhibitorsAdoptive T cell TherapyBiliary Tract CancersCancer ImmunotherapyCheckpoint Inhibitor TherapyCholangiocarcinomaVaccines

Identifiers

PMID29501212
PMCPMC6178815
OpenAlexW2765631123

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.