Evidence map›Paper›PMID 41133004›Full record

ArticleTranslational lung cancer research2025

Myelopreservation effect of trilaciclib in extensive-stage small cell lung cancer (ES-SCLC): a systematic review and meta-analysis with trial sequential analysis of randomized clinical trials.

Yiling Ding, Zhijie Deng, Xun Yuan, Yamin Shu, Jing Chen, Shiyi Cao, Qian Chu

Abstract read
In one paragraph

Article in Translational lung cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

7 authors.

Yiling Ding *Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Zhijie Deng *Department of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Xun YuanDepartment of Oncology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Yamin ShuDepartment of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Jing ChenDepartment of Pharmacy, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Shiyi CaoSchool of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Qian ChuDepartment of Oncology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID https://orcid.org/0000-0001-8192-7630

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Small cell lung cancer (SCLC) patients undergoing chemotherapy often suffer from myelosuppression, which not only increases disease burden but also significantly impairs quality of life. A novel medication, trilaciclib, has been designed to mitigate myelosuppression and protect patients from its debilitating effects. Although trilaciclib has shown promising myeloprotection ability, researchers are seeking more evidence to gain substantial insights into its efficacy and safety profile, given the limited trial results and small sample sizes. Therefore, this study pools the efficacy and safety results of existing randomized controlled trials (RCTs) through meta-analysis and assesses the reliability of findings using trial sequential analysis (TSA). Methods: Studies were searched in databases including PubMed, Embase, the Cochrane Library, and ClinicalTrials.gov. Only RCTs with extensive-stage SCLC (ES-SCLC) patients receiving trilaciclib were included, with placebo as the comparator group. Risk of Bias 2 tools were applied to evaluate the risk of bias of included studies. Meta-analysis was conducted for result synthesis with TSA to assess the robustness of results. Results: With predetermined search terms, a total of 135 studies and trials were screened, and eventually four trials were included in analysis with low risks of bias. Of the total 356 randomized patients from four trials, 195 received trilaciclib and 161 received placebo. The results indicated that trilaciclib could significantly reduce the occurrence of severe neutropenia (SN) [odds ratio (OR): 0.08; 95% confidence interval (CI): 0.04 to 0.15], shorten the duration of SN (DSN) in cycle 1 [mean difference (MD): -3.19; 95% CI: -3.96 to -2.42] and reduce the occurrence of febrile neutropenia (FN) (OR: 0.22; 95% CI: 0.08 to 0.59). Conclusions: Our meta-analysis with TSA provided robust evidence that trilaciclib could significantly protect ES-SCLC patients receiving chemotherapies from myelosuppression, thereby enabling more consistent treatment administration and potentially enhancing clinical outcomes. However, more studies are necessary to clarify indirect outcomes.

Indexed as

chemotherapymyelosuppressionsmall cell lung cancer (SCLC)systematic reviewTrilaciclib

Identifiers

PMID41133004
PMCPMC12541855

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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.