Evidence map›Paper›PMID 35347071›Full record

ReviewJournal for immunotherapy of cancer2022

Role of mass spectrometry-based serum proteomics signatures in predicting clinical outcomes and toxicity in patients with cancer treated with immunotherapy.

Yeonggyeong Park, Min Jeong Kim, Yoonhee Choi, Na Hyun Kim, Leeseul Kim, Seung Pyo Daniel Hong, Hyung-Gyo Cho, Emma Yu, Young Kwang Chae

Open access · goldAbstract readReview
In one paragraph

Review 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. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.8field-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.

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

27 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Proteomics in pancreatic cancer.Biomarker research · 2025
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. [Advances in Predictive Research of Immune Checkpoint Inhibitors-related 
Adverse Events].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2023
    Article
  17. Review
  18. Article
  19. Review
  20. Review
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 4 institutions in 1 country.

Yeonggyeong ParkDepartment of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Min Jeong KimDepartment of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Yoonhee ChoiDepartment of Internal Medicine, NewYork-Presbyterian Queens, Flushing, New York, USA.
Na Hyun KimDepartment of Internal Medicine, AMITA Health Saint Joseph Hospital Chicago, Chicago, Illinois, USA.
Leeseul KimDepartment of Internal Medicine, AMITA Health Saint Francis Hospital Evanston, Evanston, Illinois, USA.
Seung Pyo Daniel HongDepartment of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Hyung-Gyo ChoDepartment of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Emma YuDepartment of Medicine, Northwestern University, Chicago, Illinois, USA.
Young Kwang ChaeDepartment of Hematology and Oncology, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA young.chae@northwestern.edu.
Northwestern University · USNew York Hospital Queens · USSaint Francis Hospital · USSaint Joseph Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy has fundamentally changed the landscape of cancer treatment. However, only a subset of patients respond to immunotherapy, and a significant portion experience immune-related adverse events (irAEs). In addition, the predictive ability of current biomarkers such as programmed death-ligand 1 (PD-L1) remains unreliable and establishing better potential candidate markers is of great importance in selecting patients who would benefit from immunotherapy. Here, we focus on the role of serum-based proteomic tests in predicting the response and toxicity of immunotherapy. Serum proteomic signatures refer to unique patterns of proteins which are associated with immune response in patients with cancer. These protein signatures are derived from patient serum samples based on mass spectrometry and act as biomarkers to predict response to immunotherapy. Using machine learning algorithms, serum proteomic tests were developed through training data sets from advanced non-small cell lung cancer (Host Immune Classifier, Primary Immune Response) and malignant melanoma patients (PerspectIV test). The tests effectively stratified patients into groups with good and poor treatment outcomes independent of PD-L1 expression. Here, we review current evidence in the published literature on three liquid biopsy tests that use biomarkers derived from proteomics and machine learning for use in immuno-oncology. We discuss how these tests may inform patient prognosis as well as guide treatment decisions and predict irAE of immunotherapy. Thus, mass spectrometry-based serum proteomics signatures play an important role in predicting clinical outcomes and toxicity.

Indexed as

Carcinoma, Non-Small-Cell LungImmune System DiseasesLung NeoplasmsB7-H1 AntigenHumansImmunologic FactorsImmunotherapyMass SpectrometryProteomicsB7-H1 AntigenImmunologic Factorsbiomarkers, tumorCTLA-4 antigenimmunotherapyprogrammed cell death 1 receptor

Identifiers

PMID35347071
PMCPMC8961104
OpenAlexW4221112332

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.