Evidence map›Paper›PMID 29391957›Full record

ArticleCase reports in hematology2017

Sequential Use of Second-Generation Tyrosine Kinase Inhibitor Treatment and Intensive Chemotherapy Induced Long-Term Complete Molecular Response in Imatinib-Resistant CML Patient Presenting as a Myeloid Blast Crisis.

Masaaki Tsuji, Tatsuki Uchiyama, Chisaki Mizumoto, Tomoharu Takeoka, Kenjiro Tomo, Tatsuharu Ohno

Open access · goldAbstract readCase Reports
In one paragraph

Article in Case reports in hematology, 2017. 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, top 81% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

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

6 authors at 1 institution in 1 country.

Masaaki TsujiDepartment of Hematology and Immunology, Otsu Red Cross Hospital, 1-1-35, Nagara, Otsu-shi, Shiga, Japan.ORCID 0000-0001-5049-2398
Tatsuki UchiyamaDepartment of Hematology and Immunology, Otsu Red Cross Hospital, 1-1-35, Nagara, Otsu-shi, Shiga, Japan.
Chisaki MizumotoDepartment of Hematology and Immunology, Otsu Red Cross Hospital, 1-1-35, Nagara, Otsu-shi, Shiga, Japan.
Tomoharu TakeokaDepartment of Hematology and Immunology, Otsu Red Cross Hospital, 1-1-35, Nagara, Otsu-shi, Shiga, Japan.
Kenjiro TomoDepartment of Hematology and Immunology, Otsu Red Cross Hospital, 1-1-35, Nagara, Otsu-shi, Shiga, Japan.
Tatsuharu OhnoDepartment of Hematology and Immunology, Otsu Red Cross Hospital, 1-1-35, Nagara, Otsu-shi, Shiga, Japan.
Otsu Red Cross Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myeloid blast crisis of chronic myeloid leukemia (CML-MBC) is rarely seen at presentation and has a poor prognosis. There is no standard therapy for CML-MBC. It is often difficult to distinguish CML-MBC from acute myeloid leukemia expressing the Philadelphia chromosome (Ph+ AML). We present a case in which CML-MBC was seen at the initial presentation in a 75-year-old male. He was treated with conventional AML-directed chemotherapy followed by imatinib mesylate monotherapy, which failed to induce response. However, he achieved long-term complete molecular response after combination therapy involving dasatinib, a second-generation tyrosine kinase inhibitor, and conventional chemotherapy.

Identifiers

PMID29391957
PMCPMC5748101
OpenAlexW2773325069

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.