Evidence map›Paper›PMID 34568489›Full record

ArticleBioMed research international2021

Improving the Lung Cancer Clinical Trial Development by Incorporating Competing Risk Factors.

Zhu Wenbo, Zhao Qing, Wang Li, Zhu Hangju, Zhang Junying, Han Jing, Qing Rong, Feng Jifeng, Shi Meiqi

Abstract read
In one paragraph

Article in BioMed research international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Zhu WenboJiangsu Cancer Hospital, Affiliated Cancer Hospital of Nanjing Medical University, China.
Zhao QingJiangsu Cancer Hospital, Affiliated Cancer Hospital of Nanjing Medical University, China.
Wang LiJiangsu Cancer Hospital, Affiliated Cancer Hospital of Nanjing Medical University, China.
Zhu HangjuJiangsu Cancer Hospital, Affiliated Cancer Hospital of Nanjing Medical University, China.
Zhang JunyingJiangsu Cancer Hospital, Affiliated Cancer Hospital of Nanjing Medical University, China.
Han JingJiangsu Cancer Hospital, Affiliated Cancer Hospital of Nanjing Medical University, China.
Qing RongJiangsu Cancer Hospital, Affiliated Cancer Hospital of Nanjing Medical University, China.
Feng JifengJiangsu Cancer Hospital, Affiliated Cancer Hospital of Nanjing Medical University, China.ORCID https://orcid.org/0000-0002-7979-2391
Shi MeiqiJiangsu Cancer Hospital, Affiliated Cancer Hospital of Nanjing Medical University, China.ORCID https://orcid.org/0000-0002-3578-4082

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionDistinct from other diseases, as cancer progresses, both the symptoms and treatments evolve, resulting in a complex, time-dependent relationship. Many competing risk factors influence the outcome of cancer. An improved method was used to evaluate the data from 6 non-small-cell lung cancer (NSCLC) clinical trials combined in our center since 2016 to deal with the bias caused by competing risk factors.

resultsImmunotherapy had better progression-free survival than chemotherapy. (HR: 0.62, 95% CI: 0.41-0.95,

conclusionWhen the outcome caused by competing risk exists, the corresponding competing risk model method should be adopted to eliminate the bias caused by the classic survival analysis.

Indexed as

Clinical Trials as TopicAgedDisease ProgressionFemaleHumansIncidenceKaplan-Meier EstimateLung NeoplasmsMaleMiddle AgedProgression-Free SurvivalRisk Factors

Identifiers

PMID34568489
PMCPMC8457938

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Registered trials

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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.