Evidence map›Paper›PMID 38857913›Full record

ArticleJournal for immunotherapy of cancer2024

Single-cell analysis reveals cellular and molecular factors counteracting HPV-positive oropharyngeal cancer immunotherapy outcomes.

Junha Cha, Da Hee Kim, Gamin Kim, Jae-Won Cho, Euijeong Sung, Seungbyn Baek, Min Hee Hong, Chang Gon Kim, Nam Suk Sim, Hyun Jun Hong and 8 more

Registry-linked trialAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03737968 (Window of Opportunity Trial of Durvalumab), which is not on this map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT03737968 phase2unknown statusnot on this map

Window of Opportunity Trial of Durvalumab (MEDI4736) or Durvalumab/Tremelimumab as Neoadjuvant Chemotherapy to Identify Immune Dynamics in Surgically Resectable Head and Neck Cancer Patients.

TypeinterventionalSponsorYonsei UniversityRan2019 to 2023Enrolled48ConditionsStage II-IVB Operable HNSCC Oral Cavity, Hypopharynx, Oropharynx, LarynxArmsDurvalumab, durvalumab + tremelimumab
3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. 4-1BBCell reports. Medicine · 2025
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  19. Targeting of the CD161 Inhibitory Receptor Enhances Bone-Marrow-Resident Memory CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
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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

18 authors.

Junha Cha *Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
Da Hee Kim *Department of Otorhinolaryngology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Gamin Kim *Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jae-Won ChoThe Gene Lay Institute of Immunology and Inflammation, Brigham and Women's Hospital, Massachusetts General Hospital, and Harvard Medical School, Boston, MA, USA.
Euijeong SungDepartment of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
Seungbyn BaekDepartment of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
Min Hee HongDivision of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0003-3490-2195
Chang Gon KimDivision of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.
Nam Suk SimDepartment of Otorhinolaryngology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Hyun Jun HongDepartment of Otorhinolaryngology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jung Eun LeeDivision of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea.
Martin HembergThe Gene Lay Institute of Immunology and Inflammation, Brigham and Women's Hospital, Massachusetts General Hospital, and Harvard Medical School, Boston, MA, USA.
Seyeon ParkDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
Sun Ock YoonDepartment of Pathology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Sang-Jun HaDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea insuklee@yonsei.ac.kr nobelg@yuhs.ac YWKOHENT@yuhs.ac sjha@yonsei.ac.kr.ORCID http://orcid.org/0000-0002-1192-6031
Yoon Woo KohDepartment of Otorhinolaryngology, Yonsei University College of Medicine, Seoul, Republic of Korea insuklee@yonsei.ac.kr nobelg@yuhs.ac YWKOHENT@yuhs.ac sjha@yonsei.ac.kr.
Hye Ryun KimDivision of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Republic of Korea insuklee@yonsei.ac.kr nobelg@yuhs.ac YWKOHENT@yuhs.ac sjha@yonsei.ac.kr.ORCID http://orcid.org/0000-0002-1842-9070
Insuk LeeDepartment of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea insuklee@yonsei.ac.kr nobelg@yuhs.ac YWKOHENT@yuhs.ac sjha@yonsei.ac.kr.ORCID http://orcid.org/0000-0003-3146-6180

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOropharyngeal squamous cell carcinoma (OPSCC) induced by human papillomavirus (HPV-positive) is associated with better clinical outcomes than HPV-negative OPSCC. However, the clinical benefits of immunotherapy in patients with HPV-positive OPSCC remain unclear.

methodsTo identify the cellular and molecular factors that limited the benefits associated with HPV in OPSCC immunotherapy, we performed single-cell RNA (n=20) and T-cell receptor sequencing (n=10) analyses of tonsil or base of tongue tumor biopsies prior to immunotherapy. Primary findings from our single-cell analysis were confirmed through immunofluorescence experiments, and secondary validation analysis were performed via publicly available transcriptomics data sets.

resultsWe found significantly higher transcriptional diversity of malignant cells among non-responders to immunotherapy, regardless of HPV infection status. We also observed a significantly larger proportion of CD4

conclusionsWe found that CD161 TRIAL REGISTRATION NUMBER: NCT03737968.

Indexed as

ImmunotherapyOropharyngeal NeoplasmsPapillomavirus InfectionsSingle-Cell AnalysisAgedFemaleHumansMaleMiddle AgedNK Cell Lectin-Like Receptor Subfamily BKLRB1 protein, humanNK Cell Lectin-Like Receptor Subfamily Bco-inhibitory moleculeHead and Neck CancerImmune Checkpoint InhibitorImmunotherapyTumor microenvironment - TME

Identifiers

PMID38857913
PMCPMC11168198

What Socratic holds

Textmetadata
LicenceCC BY-NC
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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 Socratic graph.