Evidence map›Paper›PMID 30526517›Full record

ArticleBMC cancer2018

Ponatinib induces a sustained deep molecular response in a chronic myeloid leukaemia patient with an early relapse with a T315I mutation following allogeneic hematopoietic stem cell transplantation: a case report.

Nuno Cerveira, Rosa Branca Ferreira, Susana Bizarro, Cecília Correia, Lurdes Torres, Susana Lisboa, Joana Vieira, Rui Santos, Fernando Campilho, Carlos Pinho Vaz and 3 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in BMC cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 17% 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.

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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Role of Stem-Cell Transplantation in Leukemia Treatment.Stem cells and cloning : advances and applications · 2020
    Review
  2. Article
  3. Review
  4. 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

13 authors at 2 institutions in 1 country.

Nuno CerveiraDepartment of Genetics, Portuguese Oncology Institute, Porto, Portugal. nuno.cerveira@ipoporto.min-saude.pt.ORCID http://orcid.org/0000-0001-5098-3840
Rosa Branca FerreiraDepartment of Bone Marrow Transplantation, Portuguese Oncology Institute, Porto, Portugal.
Susana BizarroDepartment of Genetics, Portuguese Oncology Institute, Porto, Portugal.
Cecília CorreiaDepartment of Genetics, Portuguese Oncology Institute, Porto, Portugal.
Lurdes TorresDepartment of Genetics, Portuguese Oncology Institute, Porto, Portugal.
Susana LisboaDepartment of Genetics, Portuguese Oncology Institute, Porto, Portugal.
Joana VieiraDepartment of Genetics, Portuguese Oncology Institute, Porto, Portugal.
Rui SantosDepartment of Genetics, Portuguese Oncology Institute, Porto, Portugal.
Fernando CampilhoDepartment of Bone Marrow Transplantation, Portuguese Oncology Institute, Porto, Portugal.
Carlos Pinho VazDepartment of Bone Marrow Transplantation, Portuguese Oncology Institute, Porto, Portugal.
Luís LeiteDepartment of Bone Marrow Transplantation, Portuguese Oncology Institute, Porto, Portugal.
Manuel R TeixeiraDepartment of Genetics, Portuguese Oncology Institute, Porto, Portugal.
António CamposDepartment of Bone Marrow Transplantation, Portuguese Oncology Institute, Porto, Portugal.
Instituto Português de Oncologia Francisco Gentil · PTUniversidade do Porto · PT

Funding

Incyte Corp Not applicable
6 · The paper itself

Abstract

backgroundAtypical BCR-ABL1 transcripts are detected in less than 5% of patients diagnosed with chronic myeloid leukaemia (CML), of which e19a2 is the most frequently observed, with breakpoints in the micro breakpoint cluster region (μ-BCR) and coding for the p230 BCR-ABL1 protein. p230 CML is associated with various clinical presentations and courses with variable responses to first-line imatinib. CASE PRESENTATION: Here we report a case of imatinib resistance due to an E255V mutation, followed by early post-transplant relapse with a T315I mutation that achieved a persistent negative deep molecular response (MR

conclusionThis case illustrates the major interest of ponatinib as a valid treatment option for e19a2 CML patients who present a T315I mutation following relapse after HSCT.

Indexed as

Fusion Proteins, bcr-ablHematopoietic Stem Cell TransplantationHumansImatinib MesylateImidazolesLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMaleMiddle AgedMutationNeoplasm Recurrence, LocalPyridazinesRecurrenceFusion Proteins, bcr-ablImatinib MesylateImidazolesponatinibPyridazinesCMLHSCTPonatinibRelapseT315I

Identifiers

PMID30526517
PMCPMC6286606
OpenAlexW2904934367

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.