Evidence map›Paper›PMID 37395846›Full record

Trial reportJournal of cancer research and clinical oncology2023

Development of a radiomic-clinical nomogram for prediction of survival in patients with diffuse large B-cell lymphoma treated with chimeric antigen receptor T cells.

Yeye Zhou, Bin Zhang, Jiangqin Han, Na Dai, Tongtong Jia, Haiwen Huang, Shengming Deng, Shibiao Sang

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of cancer research and clinical oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 3 pooled it
2.5field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 3 syntheses or guidelines pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. The prognostic utility ofFrontiers in immunology · 2024
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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

8 authors at 2 institutions in 1 country.

Yeye Zhou *Department of Nuclear Medicine, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Bin Zhang *Department of Nuclear Medicine, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Jiangqin Han *Department of Nuclear Medicine, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Na DaiDepartment of Nuclear Medicine, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Tongtong JiaDepartment of Nuclear Medicine, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China.
Haiwen HuangInstitute of Blood and Marrow Transplantation, Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, 215006, Jiangsu, China. hhaiwen111@163.com.
Shengming DengDepartment of Nuclear Medicine, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China. dshming@163.com.
Shibiao SangDepartment of Nuclear Medicine, The First Affiliated Hospital of Soochow University, Suzhou, 215006, China. sshibiao@163.com.
Soochow University · CNFirst Affiliated Hospital of Soochow University · CN

Funding

Gusu Health Talent Program No. GSWS2020013Medical Youth Talent Project of Jiangsu Province No. QNRC2016749National Natural Science Foundation of China No. 81601522Project of State Key Laboratory of Radiation Medicine and Protection, Soochow University No. GZK1202127Suzhou People's Livelihood Science and Technology Project No. SYS2019038the Open Foundation of Nuclear Medicine Laboratory of Mianyang Central Hospital No. 2021HYX023 and 2021HYX029
6 · The paper itself

Abstract

backgroundIn our current work, an

methodsA total of 61 DLBCL cases receiving

resultsThe radiomics model that integrated R-signatures and clinical risk factors showed superior prognostic performance compared with the clinical models in terms of both PFS (C-index: 0.710 vs. 0.716; AUC: 0.776 vs. 0.712) and OS (C-index: 0.780 vs. 0.762; AUC: 0.828 vs. 0.728). For validation, the C-index of the two approaches was 0.640 vs. 0.619 and 0.676 vs. 0.699 for predicting PFS and OS, respectively. Moreover, the AUC was 0.886 vs. 0.635 and 0.778 vs. 0.705, respectively. The calibration curves indicated good agreement, and the decision curve analysis suggested that the net benefit of radiomics models was higher than that of clinical models.

conclusionsPET/CT-derived R-signature could be a potential prognostic biomarker for R/R DLBCL patients undergoing CAR-T cell therapy. Moreover, the risk stratification could be further enhanced when the PET/CT-derived R-signature was combined with clinical factors.

Indexed as

Lymphoma, Large B-Cell, DiffuseLymphoma, Non-HodgkinReceptors, Chimeric AntigenFluorodeoxyglucose F18HumansNomogramsPositron Emission Tomography Computed TomographyRetrospective StudiesT-LymphocytesFluorodeoxyglucose F18Receptors, Chimeric AntigenCAR-TDiffuse large B-cell lymphomaPET/CTPrognosisRadiomics

Identifiers

PMID37395846
PMCPMC11797235
OpenAlexW4382918320

What OpenQuestion holds

Textmetadata
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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.