Evidence map›Paper›PMID 39215800›Full record

ArticleSupportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer2024

Trilaciclib use in extensive-stage small cell lung cancer (ES-SCLC): are clinical benefits seen in the real-world setting?

Joseph Elijah, Prantesh Jain, Allison Holdsworth, Jeffrey Baron, Eugene Przespolewski, Katy Wang, Kristopher Attwood, Christina Billias, Grace K Dy

Abstract read
In one paragraph

Article in Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
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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

9 authors.

Joseph ElijahDepartment of Pharmacy, Massachusetts General Hospital, Boston, MA, USA. jelijah@umich.edu.
Prantesh JainDepartment of Medical Oncology, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Allison HoldsworthUniversity at Buffalo School of Pharmacy and Pharmaceutical Sciences, Buffalo, NY, USA.
Jeffrey BaronUniversity at Buffalo School of Pharmacy and Pharmaceutical Sciences, Buffalo, NY, USA.
Eugene PrzespolewskiUniversity at Buffalo School of Pharmacy and Pharmaceutical Sciences, Buffalo, NY, USA.
Katy WangDepartment of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Kristopher AttwoodDepartment of Biostatistics and Bioinformatics, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Christina BilliasUniversity at Buffalo School of Pharmacy and Pharmaceutical Sciences, Buffalo, NY, USA.
Grace K DyDepartment of Medical Oncology, Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrilaciclib, in comparison to placebo plus carboplatin, etoposide, ± atezolizumab (PEA), has shown significant reductions in incidence of severe neutropenia (SN) among patients with extensive-stage small cell lung cancer (ES-SCLC). Despite these findings, real-world utility remains limited.

methodsA single-center quasi-experimental study compared trilaciclib + PEA (PEAT) versus PEA in ES-SCLC patients. The study period ranged from April 1, 2021 to July 31, 2022, for the PEAT recipients and February 1, 2020, to February 28, 2021, for PEA recipients. The primary endpoint evaluated was incidence of SN after cycle 1 and during the treatment period. Secondary endpoints included measures related to myelopreservation and patient outcomes.

resultsAmong 34 PEAT and 44 PEA patients, baseline characteristics were similar, except for a higher median age (69 vs 64 years) and more males (64.7% vs 38.6%) in the PEAT cohort. The PEAT cohort exhibited a lower SN rate (3%) versus the PEA cohort (18%), with statistical significance demonstrated on multivariate analysis (p = 0.015). Additionally, the PEAT cohort also demonstrated significant reductions in red blood cell transfusion requirements (3% vs 23%; p = 0.02), grade 3-4 anemia (6% vs 25%; p = 0.03), and grade 3-4 thrombocytopenia (0% vs 11%, p = 0.045).

conclusionTrilaciclib, in combination with PEA, demonstrated an improvement in the safety profile without compromising survival outcomes in ES-SCLC patients. These findings underscore the potential benefits of incorporating trilaciclib in real-world clinical settings for enhanced patient care.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsLung NeoplasmsSmall Cell Lung CarcinomaAgedFemaleHumansMaleMiddle AgedNeoplasm StagingNeutropeniaPyrimidinesPyrrolesTriazolesPyrimidinesPyrrolesTriazolestrilaciclibAtezolizumabCarboplatinES-SCLCEtoposideNeutropeniaTrilaciclib

Identifiers

PMID39215800
PMCPMC11365831

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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.