Evidence map›Paper›PMID 38533509›Full record

ArticleFrontiers in immunology2024

Role of CD38 in anti-tumor immunity of small cell lung cancer.

Hirokazu Taniguchi, Shweta S Chavan, Andrew Chow, Joseph M Chan, Hiroshi Mukae, Charles M Rudin, Triparna Sen

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. 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

7 authors at 5 institutions in 2 countries.

Hirokazu TaniguchiDepartment of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Shweta S ChavanMarie-Josée and Henry R. Kravis Center for Molecular Oncology, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Andrew ChowDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Joseph M ChanDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Hiroshi MukaeDepartment of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Charles M RudinDepartment of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Triparna SenDepartment of Oncological Sciences, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Memorial Sloan Kettering Cancer Center · USNagasaki University · JPCornell University · USIcahn School of Medicine at Mount Sinai · USMolecular Oncology (United States) · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
Coordinating center for the NCI small cell lung cancer research consortiumU24CA213274 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Lauren Averett Byers, JOHN D. MINNA · 2017 to 2026
$12.9M
Novel therapeutic development for small cell lung cancerR35CA263816 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Charles M. Rudin · 2021 to 2026
$6.3M
Determinants of acquired resistance in small cell lung cancerR01CA197936 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI RUDIN, CHARLES M. · 2016 to 2020
$3.1M
Targeting replication stress signaling to overcome immune evasion in small cell lung cancerR01CA258784 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SEN, TRIPARNA · 2021 to 2025
$2.4M
Assessment of Tim-4+ Pleural Macrophages as Negative Regulators of Anti-Tumor T Cell Immunity in Lung CancerK08CA248723 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI CHOW, ANDREW · 2020 to 2022
$602k
NCI NIH HHS K08 CA248723NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA197936NCI NIH HHS R01 CA258784NCI NIH HHS R35 CA263816NCI NIH HHS U24 CA213274
6 · The paper itself

Abstract

Introduction: Immune checkpoint blockade (ICB) with or without chemotherapy has a very modest benefit in patients with small cell lung cancer (SCLC). SCLC tumors are characterized by high tumor mutation burden (TMB) and low PD-L1 expression. Therefore, TMB and PD-L1 do not serve as biomarkers of ICB response in SCLC. CD38, a transmembrane glycoprotein, mediates immunosuppression in non-small cell lung cancer (NSCLC). In this brief report, we highlight the potential role of CD38 as a probable biomarker of immunotherapy response in SCLC. Methods: We evaluated the role of CD38 as a determinant of tumor immune microenvironment in SCLC with bulk and single-cell transcriptomic analyses and protein assessments of clinical samples and preclinical models, including CD38 Results: In SCLC clinical samples, Conclusion: Our study provides a preliminary but important direction toward exploring CD38 as a potential biomarker of ICB response and CD38 blockade as a combination strategy for chemo-immunotherapy in SCLC.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsSmall Cell Lung CarcinomaB7-H1 AntigenBiomarkersCisplatinEtoposideHumansTumor MicroenvironmentB7-H1 AntigenBiomarkersCisplatinEtoposideCD38immune checkpoint blockadelung cancerresistancesmall cell lung cancer

Identifiers

PMID38533509
PMCPMC10963403
OpenAlexW4392712961

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.