Evidence map›Paper›PMID 31092729›Full record

ArticleJCI insight2019

Titin mutation associated with responsiveness to checkpoint blockades in solid tumors.

Qingzhu Jia, Jun Wang, Ning He, Ji He, Bo Zhu

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed
9.8field-weighted citation impact, top 1% 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

116 citing papers in PubMed, 173 citations in OpenAlex.

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  16. Cross-talk of mFrontiers in immunology · 2025
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56 more citing papers are in PubMed but not listed here.

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

5 authors at 3 institutions in 1 country.

Qingzhu JiaInstitute of Cancer, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Jun WangChongqing Key Laboratory of Immunotherapy, Chongqing, China.
Ning HeDepartment of Cancer Immunotherapy, Shandong Cancer Hospital Affiliated to Shandong University, Shandong, China.
Ji HeGloriousMed Technology Co., Ltd. Beijing, China.
Bo ZhuInstitute of Cancer, Xinqiao Hospital, Third Military Medical University, Chongqing, China.
Army Medical University · CNAnnoroad Gene Technology (China) · CNShandong Tumor Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint blockade (ICB) immunotherapy induces potent antitumor immunity across multiple solid tumors, although few patients respond well to this therapy. An emerging biomarker for predicting responsiveness to ICB immunotherapy is tumor mutational burden (TMB). Although several surrogate biomarkers, including deficient mismatch repair, TP53/KRAS mutations, and comutations in DNA damage response pathways, have been shown to be effective for predicting the response to checkpoint blockade immunotherapy, each is positive for only a small cohort of candidates, and many potential responders to ICB are inevitably missed. Here, we found that titin (TTN), which is frequently detected in solid tumors, is associated with increased TMB and correlated with objective response to ICB. In 7 public clinical cohorts, all patients with mutated TTN showed longer progression-free survival or overall survival than those with wild-type status. Furthermore, an improved objective response rate and higher TMB were identified in cohorts with accessible information. Identification of TTN mutation as a predictor of improved outcomes in response to ICBs provides a clinically feasible assessment for estimating TMB and ICB therapy outcomes.

Indexed as

MutationAntibodies, Monoclonal, HumanizedBiomarkers, TumorComputational BiologyConnectinHumansImmunotherapyLung NeoplasmsMelanomaNeoplasmsNivolumabProgrammed Cell Death 1 ReceptorSurvival AnalysisAntibodies, Monoclonal, HumanizedBiomarkers, TumorConnectinNivolumabPDCD1 protein, humanpembrolizumabProgrammed Cell Death 1 ReceptorBioinformaticsCancer immunotherapyTherapeutics

Identifiers

PMID31092729
PMCPMC6542599
OpenAlexW2945858728

What OpenQuestion holds

Textmetadata
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.