Evidence map›Paper›PMID 35875127›Full record

ArticleFrontiers in oncology2022

A New Nomogram and Risk Stratification of Brain Metastasis by Clinical and Inflammatory Parameters in Stage III Small Cell Lung Cancer Without Prophylactic Cranial Irradiation.

Jianjian Qiu, Dongmei Ke, Yilin Yu, Hancui Lin, Qunhao Zheng, Hui Li, Hongying Zheng, Lingyun Liu, Zhiping Wang, Yahua Wu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 9 citations in OpenAlex.

  1. 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

12 authors at 2 institutions in 1 country.

Jianjian QiuFujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, China.
Dongmei KeFujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, China.
Yilin YuFujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, China.
Hancui LinFujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, China.
Qunhao ZhengFujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, China.
Hui LiFujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, China.
Hongying ZhengFujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, China.
Lingyun LiuFujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, China.
Zhiping WangFujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, China.
Yahua WuFujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, China.
Tianxiu LiuFujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, China.
Jiancheng LiFujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, China.
Fujian Medical University · CNFujian Provincial Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: This study was conducted to determine risk factors for developing brain metastasis (BM) and to predict brain metastasis free survival (BMFS) and overall survival (OS) by combining several clinical parameters and inflammatory indexes. Materials and Methods: A nomogram and risk stratification were developed based on multivariate analysis results. The prognostic index (PI) predicting the high risk of BM was calculated by multiplying the weighted factor (β coefficient) with each variable. Results: Thirty-two of one hundred patients (32.0%) developed BM. Multivariate cox regression analysis revealed that concurrent chemoradiotherapy (CCRT; hazard ratio (HR), 3.356; p = 0.020), monocyte-lymphocyte ratio (MLR; HR, 4.511; p = 0.002), neutrophil-lymphocyte ratio (NLR; HR, 4.023; p = 0.033), and prognostic-nutrition index (PNI; HR, 2.902; p = 0.018) were independent prognostic factors of BMFS. The nomogram has good accuracy in predicting BMFS, and the C-index was 0.73. The ROC curve showed that these risk factors have good discriminant ability. Similarly, tumor location (HR, 1.675; p = 0.035) and MLR (HR, 2.076; p = 0.013) were independent prognostic factors of OS. In the subgroup analysis of OS, the good group had a better prognosis than the other groups. Risk stratification by PI: the high-risk group had worse BMFS than the low-risk group, which also has certain practical significance for clinical practice in OS. Conclusion: We developed a nomogram and corresponding risk stratification in stage III SCLC patients who developed BM. This model and risk stratification can help clinicians improve patient treatment management and better deliver personalized therapy.

Indexed as

brain metastasisnomogramrisk factorrisk stratificationsmall cell lung cancer

Identifiers

PMID35875127
PMCPMC9300937
OpenAlexW4284888838

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.