Evidence map›Paper›PMID 41567666›Full record

ArticleFrontiers in medicine2025

Toward the future management of patients with CML and Ph + ALL: real-world safety insights from dasatinib pharmacovigilance.

Zhen Lu, Guangbin Shang, Yingjian Zeng, Xiaonan Lu

Abstract read
In one paragraph

Article in Frontiers in medicine, 2025. 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

4 authors.

Zhen LuThe Affiliated Hospital of Jiangxi University of Chinese Medicine, Nanchang, China.
Guangbin ShangResearch Center for Differentiation and Development of Basic Theory of Traditional Chinese Medicine, Nanchang, China.
Yingjian ZengThe Affiliated Hospital of Jiangxi University of Chinese Medicine, Nanchang, China.
Xiaonan LuSchool of Chinese Medicine, Jiangxi University of Chinese Medicine, Nanchang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Dasatinib, a second-generation BCR-ABL1 tyrosine kinase inhibitor, has transformed treatment for chronic myeloid leukemia and Philadelphia chromosome-positive acute lymphoblastic leukemia. However, its broad kinase inhibition leads to distinct adverse events (AEs), requiring systematic post-marketing surveillance. Objective: To evaluate dasatinib-associated AEs using the United States Food and Drug Administration Adverse Event Reporting System (FAERS) and identify potential safety signals. Methods: We extracted FAERS reports (Q1 2004-Q4 2024) listing dasatinib as the primary suspect drug, submitted by physicians or pharmacists. After data cleaning, AEs were coded using MedDRA terminology. Signal detection was performed with four disproportionality methods (ROR, PRR, BCPNN, MGPS). Time-to-onset was analyzed using Weibull models, with subgroup analyses by demographic and clinical characteristics. Results: Among 7,213 cases, respiratory disorders were the most prominent signal (ROR = 2.74). A total of 1,951 significant signals were identified, 113 confirmed by all algorithms. Strongest disproportionality signals included blast cell proliferation (ROR = 518.94), primary effusion lymphoma (ROR = 181.38), and allogeneic bone marrow transplantation therapy (ROR = 171.48). Common AEs were pleural effusion ( Conclusion: This large FAERS analysis characterized known respiratory complications of dasatinib, particularly pleural effusion, and identified several rare but potentially relevant safety signals hepatotoxicity, cardiovascular events, and novel AEs such as alveolar proteinosis and cytomegalovirus-related complications. The early failure pattern underscores the need for intensive monitoring during initiation and continued vigilance during long-term therapy. These findings provide real-world, hypothesis-generating evidence to optimize safety management and inform future clinical investigations, and should be interpreted with caution in view of the inherent limitations of spontaneous reporting data.

Indexed as

adverse eventschronic myeloid leukemiadasatinibFAERSpharmacovigilancesignal detectiontyrosine kinase inhibitor

Identifiers

PMID41567666
PMCPMC12815812

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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.