Evidence map›Paper›PMID 41642397›Full record

SynthesisClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2026

Efficacy and safety of trilaciclib to prevent chemotherapy-induced myelosuppression in advanced solid tumors: a systematic review and meta-analysis.

Muhammad Ahmed, Muhammad Umer, F N U Deeksha, Rimsha Shahid, Ahsun Rizwan Siddiqi, Talha Zartash Ahmad, Hasna Panhwar, Shafaq Zahid, Abdullah Zia, Bismah Azam and 5 more

Abstract readSystematic ReviewMeta-Analysis
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In one paragraph

Synthesis in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

15 authors.

Muhammad AhmedDepartment of Internal Medicine, Henry Ford Macomb Hospital, Clinton Township, MI, USA.
Muhammad UmerDepartment of Internal Medicine, King Edward Medical University, Lahore, Pakistan.
F N U DeekshaPost Graduate Institute of Medical Education and Research, Chandigarh, India.
Rimsha ShahidDepartment of Oncology, Ziauddin University Hospital, Karachi, Pakistan.
Ahsun Rizwan SiddiqiDepartment of Internal Medicine, Henry Ford St. John Hospital, Detroit, MI, USA. ahsun23@gmail.com.ORCID http://orcid.org/0000-0003-4699-6221
Talha Zartash AhmadDepartment of Internal Medicine, King Edward Medical University, Lahore, Pakistan.
Hasna PanhwarJinnah Sindh Medical University, Karachi, Pakistan.
Shafaq ZahidDepartment of Internal Medicine, King Edward Medical University, Lahore, Pakistan.
Abdullah ZiaAmeer-Ud-Din Medical College, Lahore, Pakistan.
Bismah AzamDow University of Health Sciences, Karachi, Pakistan.
Amina Yousaf BajwaDepartment of Internal Medicine, Icahn School of Medicine at Mount, Sinai Valley Health System, Paramus, NJ, USA.
Osaf Ali KhanDepartment of Internal Medicine, Naples Comprehensive Health, Naples, FL, USA.
Aqeeb Ur RehmanDepartment of Internal Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
Muhammad Salman FaisalOU Health Stephenson Cancer Center, Oklahoma, OK, USA.
Niluka WeerakoonDepartment of Internal Medicine, Henry Ford Macomb Hospital, Clinton Township, MI, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrilaciclib is a cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitor that has shown promise in mitigating chemotherapy-induced myelosuppression (CIM). This meta-analysis aims to provide a comprehensive and clinically relevant quantification of trilaciclib's effectiveness in reducing CIM and its potential impact on outcomes in adult patients with solid tumors.

methodsWe performed a systematic review and meta-analysis of randomized controlled trials (RCTs) and observational studies evaluating trilaciclib administered along with chemotherapy in adult patients (≥ 18 years) with advanced or metastatic solid tumors. Databases searched included PubMed, Embase, the Cochrane Library, and major trial registries (ClinicalTrials.gov, EU Clinical Trials Register, ICTRP) up to May 21, 2025. Primary outcomes were incidence of grade 3/4 neutropenia, febrile neutropenia (FN), need for granulocyte-colony stimulating factors (G-CSF)/erythropoiesis-stimulating agents (ESA), and need for red blood cell/platelet transfusions. Efficacy endpoints included progression-free survival (PFS), overall survival (OS), and objective response rate (ORR). Pooled odds ratios (OR) or hazard ratios (HR) were calculated using a random-effects model. Heterogeneity was assessed with the I

resultsTen studies with a total of 979 patients were included, with 586 receiving trilaciclib alongside chemotherapy and 393 receiving chemotherapy alone. Pooled analysis showed that trilaciclib decreased the incidence of grade 3/4 neutropenia by 79% (OR = 0.21; 95% CI: 0.08-0.52; I

conclusionTrilaciclib significantly reduced CIM and the need for hematopoietic support during chemotherapy. It also showed a positive impact on efficacy outcomes without compromising chemotherapy effectiveness or increasing toxicity. Overall, our findings support trilaciclib's evolving role as a promising adjunct to chemotherapy protocols in appropriately selected patients.

Indexed as

Antineoplastic AgentsNeoplasmsPyrimidinesPyrrolesHumansNeutropeniaSpiro CompoundsAntineoplastic AgentsPyrimidinesPyrrolesSpiro CompoundstrilaciclibCancerChemotherapyMyelosuppressionNeutropeniaTrilaciclib

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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.