Evidence map›Paper›PMID 33968765›Full record

ArticleFrontiers in oncology2021

Co-Occurring Alteration of NOTCH and DDR Pathways Serves as Novel Predictor to Efficacious Immunotherapy in NSCLC.

Zhimin Zhang, Yanyan Gu, Xiaona Su, Jing Bai, Wei Guan, Jungang Ma, Jia Luo, Juan He, Bicheng Zhang, Mingying Geng and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
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  7. Article
  8. Review
  9. Roles of Notch Signaling in the Tumor Microenvironment.International journal of molecular sciences · 2022
    Review
  10. 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

14 authors at 5 institutions in 1 country.

Zhimin ZhangCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.
Yanyan GuDepartment of Nutrition, Changzheng Hospital, Second Military Medical University, Shanghai, China.
Xiaona SuCancer Center, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Jing BaiGeneplus-Beijing Institute, Beijing, China.
Wei GuanCancer Center, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Jungang MaCancer Center, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Jia LuoCancer Center, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Juan HeCancer Center, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Bicheng ZhangCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.
Mingying GengCancer Center, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Xuefeng XiaGeneplus-Beijing Institute, Beijing, China.
Yanfang GuanGeneplus-Beijing Institute, Beijing, China.
Cheng ShenDepartment of Thoracic Surgery, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Chuan ChenCancer Center, Daping Hospital, Army Medical University (Third Military Medical University), Chongqing, China.
Army Medical University · CNDaping Hospital · CNRenmin Hospital of Wuhan University · CNSecond Military Medical University · CNWuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although immune checkpoint inhibitors (ICIs) have shown remarkable benefit for treatment of advanced non-small lung cancer (NSCLC), only a minority of patients can achieve durable responses and the most patients produce an ultra-rapid progressive disease. Here, we collected the availably published datasets and mined the determinants of response to immunotherapy on pathway levels. One hundred six NSCLC patients treated with immunotherapy were combined from Rizvi et al. and Hellman et al. studies (whole exon sequencing). Two independent validation datasets consisted of the MSKCC cohort (targeted sequencing) and data by Anagnostou and colleagues (whole exon sequencing). The Cancer Genome Atlas (TCGA) somatic mutation and gene expression data were applied to explore the immunobiology features. In the first combined cohort, we detected NOTCH pathway altered in 71% patients with durable clinical benefit (DCB) while only 36% among no durable benefit (NDB) (p = 0.005). Compared to NDB group, co-occurrence of NOTCH and at least two DDR (co-DDR) pathway was discovered in DCB group and contributed to a prolonged progression-free survival (PFS) [22.1

Indexed as

co-occurring mutationsDDR pathwayimmunotherapynon-small cell lung cancerNOTCH pathwaypredictive biomarker

Identifiers

PMID33968765
PMCPMC8100434
OpenAlexW3158420671

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.