Evidence map›Paper›PMID 29033451›Full record

ReviewThe American journal of case reports2017

Dasatinib and Azacitidine Followed by Haploidentical Stem Cell Transplant for Chronic Myeloid Leukemia with Evolving Myelodysplasia: A Case Report and Review of Treatment Options.

Fabian Lang, Lydia Wunderle, Heike Pfeifer, Susanne Schnittger, Gesine Bug, Oliver G Ottmann

Registry-linked trialOpen access · greenAbstract readCase ReportsReview
In one paragraph

Review in The American journal of case reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05042531 (Clinical Research for Azacitidine Combined With Low-dose Dasatinib in Maintenance Therapy of Acute Myeloid Leukemia), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 35% of its field
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.

NCT05042531 naunknown statusnot on this mapstarted 2021, after this paper: background citation

Clinical Research for Azacitidine Combined With Low-dose Dasatinib in Maintenance Therapy of Acute Myeloid Leukemia

TypeinterventionalSponsorLanZhou UniversityRan2021 to 2023Enrolled30ConditionsAcute Myeloid LeukemiaArmsAzacitidine, Dasatinib
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

6 authors at 4 institutions in 2 countries.

Fabian LangDepartment of Hematology/Oncology, Goethe University Hospital, Frankfurt am Main, Germany.
Lydia WunderleDepartment of Hematology/Oncology, Goethe University Hospital, Frankfurt am Main, Germany.
Heike PfeiferDepartment of Hematology/Oncology, Goethe University Hospital, Frankfurt am Main, Germany.
Susanne SchnittgerMLL Munich Leukemia Laboratory, Munich, Germany.
Gesine BugDepartment of Hematology/Oncology, Goethe University Hospital, Frankfurt am Main, Germany.
Oliver G OttmannDivision of Cancer and Genetics, School of Medicine, Cardiff University, Cardiff, Wales, United Kingdom.
Goethe University Frankfurt · DEUniversity Hospital Frankfurt · DECardiff University · GBMunich Leukemia Laboratory (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND CML presenting with a variant Philadelphia translocation, atypical BCR-ABL transcript, additional chromosomal aberrations, and evolving MDS is uncommon and therapeutically challenging. The prognostic significance of these genetic findings is uncertain, even as singular aberrations, with nearly no data on management and outcome when they coexist. MDS evolving during the course of CML may be either treatment-associated or an independently coexisting disease, and is generally considered to have an inferior prognosis. Tyrosine kinase inhibitors (TKI) directed against BCR-ABL are the mainstay of treatment for CML, whereas treatment modalities that may be utilized for MDS and CML include allogeneic stem cell transplant and - at least conceptually - hypomethylating agents. CASE REPORT Here, we describe the clinical course of such a patient, demonstrating that long-term combined treatment with dasatinib and azacitidine for coexisting CML and MDS is feasible and well tolerated, and may be capable of slowing disease progression. This combination therapy had no deleterious effect on subsequent potentially curative haploidentical bone marrow transplantation. CONCLUSIONS The different prognostic implications of this unusual case and new therapeutic options in CML are discussed, together with a review of the current literature on CML presenting with different types of genomic aberrations and the coincident development of MDS. Additionally, this case gives an example of long-term combined treatment of tyrosine kinase inhibitors and hypomethylating agents, which could be pioneering in CML treatment.

Indexed as

Stem Cell TransplantationAdultAzacitidineDasatinibDrug Therapy, CombinationFemaleHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMyelodysplastic SyndromesProtein Kinase InhibitorsAzacitidineDasatinibProtein Kinase Inhibitors

Identifiers

PMID29033451
PMCPMC5652250
OpenAlexW2766720469

What OpenQuestion holds

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Registered trials

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.