Evidence map›Paper›PMID 40361493›Full record

ArticleCancers2025

CDK4/6 Inhibitors-Induced Macrocytosis Is Not Associated with Hemolysis and Does Not Impact Hemoglobin Homeostasis.

Tiago Barroso, Leila Costa, Lisa Gonçalves, Vanessa Patel, João Araújo, Inês Pinho, Carolina Monteiro, Miguel Esperança-Martins, Catarina Abreu, Rita Teixeira de Sousa and 5 more

Abstract read
In one paragraph

Article in Cancers, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. Article
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

15 authors.

Tiago BarrosoMedical Oncology Department, Unidade Local de Saúde Santa Maria, 1649-03 Lisbon, Portugal.ORCID 0000-0003-4854-1642
Leila CostaPharmacy Department, Unidade Local de Saúde Santa Maria, 1649-03 Lisbon, Portugal.
Lisa GonçalvesMedical Oncology Department, Unidade Local de Saúde Santa Maria, 1649-03 Lisbon, Portugal.ORCID 0000-0002-3431-5217
Vanessa PatelMedical Oncology Department, Unidade Local de Saúde Santa Maria, 1649-03 Lisbon, Portugal.
João AraújoMedical Oncology Department, Unidade Local de Saúde Santa Maria, 1649-03 Lisbon, Portugal.
Inês PinhoMedical Oncology Department, Unidade Local de Saúde Santa Maria, 1649-03 Lisbon, Portugal.
Carolina MonteiroMedical Oncology Department, Unidade Local de Saúde Santa Maria, 1649-03 Lisbon, Portugal.
Miguel Esperança-MartinsMedical Oncology Department, Unidade Local de Saúde Santa Maria, 1649-03 Lisbon, Portugal.ORCID 0000-0002-6858-7341
Catarina AbreuMedical Oncology Department, Unidade Local de Saúde Santa Maria, 1649-03 Lisbon, Portugal.
Rita Teixeira de SousaMedical Oncology Department, Unidade Local de Saúde Santa Maria, 1649-03 Lisbon, Portugal.
Helena PaisMedical Oncology Department, Unidade Local de Saúde Santa Maria, 1649-03 Lisbon, Portugal.
Gonçalo Nogueira-CostaMedical Oncology Department, Unidade Local de Saúde Santa Maria, 1649-03 Lisbon, Portugal.ORCID 0000-0002-1127-052X
Sofia TorresMedical Oncology Department, Unidade Local de Saúde Santa Maria, 1649-03 Lisbon, Portugal.
Leonor Abreu RibeiroMedical Oncology Department, Unidade Local de Saúde Santa Maria, 1649-03 Lisbon, Portugal.
Luís Marques da CostaMedical Oncology Department, Unidade Local de Saúde Santa Maria, 1649-03 Lisbon, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCDK 4/6 inhibitors (CDK4/6is) are the first-line treatment for metastatic luminal-like breast cancer (BC). These drugs induce macrocytosis without anemia in most patients. The mechanism for the red blood cell (RBC) changes is unknown. In vitro and animal studies show that RBCs from CDK6-knockout mice have increased membrane fragility, but the clinical impact of CDK4/6is on human RBC lifespan is not known. We sought to determine the impact of CDK4/6is on RBC lifespan and detect changes in the regulation of hemoglobin production. Using the mean corpuscular volume (MCV) measurements at several time points, we can study the evolution of MCV, mean corpuscular hemoglobin concentration (MCHC), and RBC count over time. From this, one can estimate the RBC lifespan under CDK4/6is.

methodsWe performed a unicentric retrospective study. Based on published models of RBC population dynamics, we have coded a biologically inspired model which allowed us to extract values for biological parameters, including the RBC lifespan.

resultsA total of 122 patients were identified, and 1959 laboratory measurements were analyzed. After the pre-treatment RBCs were replaced, the mean MCV increased by 12.6 femtoliter (fL) (95% Bayesian credible interval [CdI] 13-14), the MCHC increased slightly by 0.69 g/dL (95% CdI 0.42-0.96), and the RBC count decreased by 0.77 × 10 DISCUSSION AND

conclusionsThese findings suggest that, despite changes in RBC volume, CDK4/6is do not predispose patients to RBC destruction and do not impair regulation of hemoglobin homeostasis. We show that CDK4/6is do not decrease the RBC lifespan in pre-treatment erythrocytes. Unfortunately, this method cannot determine the lifespan of post-treatment RBCs, but further research could help answer this question.

Indexed as

breast cancerCDK4/6 inhibitorendocrine therapyhematological toxicityred blood cell

Identifiers

PMID40361493
PMCPMC12071847

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.