Evidence map›Paper›PMID 35693614›Full record

ArticleJournal of thoracic disease2022

Analysis of the prognostic role and biological characteristics of circulating tumor cell-associated white blood cell clusters in non-small cell lung cancer.

Zheng Li, Liwen Fan, Yun Wu, Yuxu Niu, Xuelin Zhang, Bin Wang, Yuanshan Yao, Chunji Chen, Ning Qi, Daisy Dandan Wang and 3 more

Abstract read
In one paragraph

Article in Journal of thoracic disease, 2022. 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
–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.

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.

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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

13 authors.

Zheng Li *Department of Thoracic Surgery, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Liwen Fan *Department of Thoracic Surgery, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Yun WuDepartment of Thoracic Surgery, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Yuxu NiuDepartment of Thoracic Surgery, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Xuelin ZhangDepartment of Thoracic Surgery, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Bin WangDepartment of Thoracic Surgery, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Yuanshan YaoDepartment of Thoracic Surgery, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Chunji ChenDepartment of Thoracic Surgery, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Ning QiDepartment of Vascular Surgery, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Daisy Dandan WangCytelligen, San Diego, CA, USA.
Peter Ping LinCytelligen, San Diego, CA, USA.
Dongfang TangDepartment of Thoracic Surgery, Huadong Hospital Affiliated to Fudan University, Shanghai, China.
Wen GaoDepartment of Thoracic Surgery, Huadong Hospital Affiliated to Fudan University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Recently, circulating tumor-cell-associated white blood cell (CTC-WBC) clusters have been reported to have prognostic value in some cancers. The prognostic role of CTC-WBC clusters in lung cancer has not yet been elucidated. Very little information is available about the biological characteristics of CTC-WBC clusters. Methods: A total of 82 patients with non-small cell lung cancer (NSCLC) were included in this study, and 61 patients with advanced-stage disease were closely followed-up. All patients had blood drawn prior to treatment. Subtraction enrichment and immunostaining-fluorescence Results: Firstly, CTC-WBC clusters appeared more in the advanced (stage III and IV) stage (P=0.043) than in the early stage. Furthermore, the multivariable analysis (Cox proportional hazards model) revealed that the high-CTC (≥7/6 mL) group and CTC-WBC clusters (≥1/6 mL) positive group both had significantly worse PFS, with a hazard ratio (HR) of 2.89 [95% confidence interval (CI): 1.36-6.17, P=0.006] and 2.18 (95% CI: 1.07-4.43, P=0.031), respectively. In the conjoint analysis, compared to patients with <7 CTCs/6 mL without CTC-WBC clusters, patients with ≥7 CTCs/6 mL with CTC-WBC clusters had the highest risk of progression (HR =7.13, 95% CI: 2.51-20.23, P<0.001). In addition, the presence of ≥3-cell CTC-WBC clusters in patients may indicate a shorter PFS (P<0.05) and a higher risk of progression (HR =2.90, 95% CI: 1.06-7.89, P=0.037). Furthermore, compared with the characteristics of the total CTCs, almost all of the CTCs that could recruit WBCs were large cells (≥5 µm) and exhibited polyploidy (≥ tetraploid) (both P<0.01). Conclusions: The presence of CTC-WBC clusters was an independent prognostic factor for advanced NSCLC. The joint analysis of CTCs and CTC-WBC clusters could provide additional prognostic value to the enumeration of CTCs alone. Besides, most of the CTCs in CTC-WBC clusters were large polyploid cells.

Indexed as

circulating tumor-cell-associated white blood cell cluster (CTC-WBC cluster)Circulating tumor cell (CTC)non-small cell lung cancer (NSCLC)progression-free survival (PFS)

Identifiers

PMID35693614
PMCPMC9186234

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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.