Evidence map›Paper›PMID 35705312›Full record

ArticleJournal for immunotherapy of cancer2022

Increase in serum choline levels predicts for improved progression-free survival (PFS) in patients with advanced cancers receiving pembrolizumab.

Geoffrey Alan Watson, Enrique Sanz-Garcia, Wen-Jiang Zhang, Zhihui Amy Liu, Sy Cindy Yang, Ben Wang, Shaofeng Liu, Shawn Kubli, Hal Berman, Thomas Pfister and 12 more

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.4field-weighted citation impact, top 6% 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.

NCT02644369 phase2active not recruitingnot on this map

Investigator-initiated Phase II Study of Pembrolizumab Immunological Response Evaluation

TypeinterventionalSponsorUniversity Health Network, TorontoRan2016 to 2026Enrolled100ConditionsSquamous Cell Cancer of Head and Neck, Triple Negative Breast Cancer, Epithelial Ovarian Cancer, Malignant MelanomaArmsPembrolizumab
NCT03702309 recruitingnot on this map

Liquid Biopsy Evaluation and Repository Development at Princess Margaret

TypeobservationalSponsorUniversity Health Network, TorontoRan2017 to 2026Enrolled2,500ConditionsCancer, Breast Cancer, Lung Cancer, Colon Cancer
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
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  7. Article
  8. T cells at the interface of neuroimmune communication.The Journal of allergy and clinical immunology · 2024
    Review
  9. Review
  10. Review
  11. Acetylcholine-producing CD4 T cells regulate vasculature in humans.Proceedings of the National Academy of Sciences of the United States of America · 2023
    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

22 authors at 3 institutions in 1 country.

Geoffrey Alan Watson *Division of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.ORCID 0000-0003-1962-7893
Enrique Sanz-Garcia *Division of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Wen-Jiang ZhangDivision of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Zhihui Amy LiuBiostatistics, Princess Margaret Hospital Cancer Centre, Toronto, Ontario, Canada.
Sy Cindy YangMedical Biophysics, University of Toronto, Toronto, Ontario, Canada.
Ben WangLaboratory Medicine and Pathobiology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Shaofeng LiuImmunology, University of Toronto, Toronto, Ontario, Canada.
Shawn KubliImmunology, University of Toronto, Toronto, Ontario, Canada.
Hal BermanLaboratory Medicine and Pathobiology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Thomas PfisterLaboratory Medicine and Pathobiology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Sofia GentaDivision of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Anna SpreaficoDivision of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.ORCID 0000-0002-3034-3042
Aaron R HansenDivision of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Philippe L BedardDivision of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Stephanie LheureuxDivision of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.ORCID 0000-0003-4405-5890
Albiruni Abdul RazakDivision of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Dave CesconDivision of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Marcus O ButlerDivision of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Wei XuBiostatistics, Princess Margaret Hospital Cancer Centre, Toronto, Ontario, Canada.
Tak W MakImmunology, University of Toronto, Toronto, Ontario, Canada.
Lillian L Siu *Division of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada lillian.siu@uhn.ca.
Eric Chen *Division of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.ORCID 0000-0002-4581-8848
University Health Network · CAUniversity of Toronto · CAPrincess Margaret Cancer Centre · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent studies have demonstrated that T cells can induce vasodilation in a choline-acetyltransferase dependent manner, leading to an increase in T cell migration to infected tissues in response to viral infection, but its role in cancer is unclear. Choline acetyltransferase catalyzes the production of acetylcholine from choline and acetyl-CoA, however, acetylcholine is challenging to quantify due to its extremely short half-life while choline is stable. This study aims to correlate serum choline levels in patients with advanced solid tumors receiving pembrolizumab with treatment outcomes.

methodsBlood samples were collected at baseline and at week 7 (pre-cycle 3) in patients treated with pembrolizumab in the INvestigator-initiated Phase 2 Study of Pembrolizumab Immunological Response Evaluation phase II trial (NCT02644369). Samples were analyzed for choline and circulating tumor DNA (ctDNA). Multivariable Cox models were used to assess the association between choline and overall survival (OS) and progression-free survival (PFS) when including ΔctDNA

resultsA total of 106 pts were included in the analysis. With a median follow-up of 12.6 months, median PFS and OS were 1.9 and 13.7 months, respectively. An increase in serum choline level at week 7 compared with baseline (Δcholine

conclusionsThis is the first exploratory report of serum choline levels in pan-cancer patients receiving pembrolizumab. The association between improved PFS and Δcholine TRIAL REGISTRATION NUMBER: NCT03702309.

Indexed as

Antineoplastic Agents, ImmunologicalCirculating Tumor DNANeoplasmsAcetylcholineAntibodies, Monoclonal, HumanizedB7-H1 AntigenBiomarkers, TumorCholineHumansProgression-Free SurvivalAcetylcholineAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalB7-H1 AntigenBiomarkers, TumorCholineCirculating Tumor DNApembrolizumabClinical Trials as TopicImmunotherapyProgrammed Cell Death 1 ReceptorTherapies, InvestigationalTumor Microenvironment

Identifiers

PMID35705312
PMCPMC9204435
OpenAlexW4282947288

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.