Evidence map›Paper›PMID 29032513›Full record

ArticleInternational journal of hematology2018

Sudden blast phase in chronic myeloid leukemia developed during nilotinib therapy after major molecular response was achieved.

Yosuke Okada, Ken Sato, Shinichi Kobayashi, Shigeki Nagao, Kosuke Takano, Masahiro Teramoto, Noriaki Tachi, Toshikuni Kawamura, Toshikatsu Horiuchi, Shoichiro Kato and 6 more

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in International journal of hematology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

16 authors at 2 institutions in 1 country.

Yosuke OkadaDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan. fukurora_mochi@yahoo.co.jp.
Ken SatoDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan.
Shinichi KobayashiDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan.
Shigeki NagaoDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan.
Kosuke TakanoDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan.
Masahiro TeramotoDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan.
Noriaki TachiDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan.
Toshikuni KawamuraDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan.
Toshikatsu HoriuchiDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan.
Shoichiro KatoDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan.
Reina SagaDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan.
Takaaki MaekawaDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan.
Takeshi YamamuraDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan.
Junichi WatanabeDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan.
Ayako KobayashiDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan.
Fumihiko KimuraDivision of Hematology, Department of Internal Medicine, National Defense Medical College Hospital, 3-2 Namiki, Tokorozawa, Saitama, 359-0042, Japan.
National Defense Medical College · JPNational Defense Medical College Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sudden blast phase (SBP) is a rare event in which patients with chronic myeloid leukemia (CML) in complete cytogenetic response (CCyR) rapidly progress to the blast phase. Few patients on second-generation tyrosine kinase inhibitors (2nd TKIs) have been reported to develop SBP. Here, we report a 45-year-old man diagnosed with CML in the chronic phase in April 2008 and immediately started on imatinib therapy. He achieved CCyR 12 months after starting imatinib therapy. Imatinib was followed by treatment with the 2nd TKIs nilotinib and dasatinib from January 2011 to yield a better response. He achieved major molecular response (MMR) during dasatinib therapy in February 2012, but did not tolerate dasatinib well; hence, he was switched to nilotinib in July 2012. In December 2015, he presented at our hospital with fever and lumbago. A complete blood count revealed a white blood cell count of 30,500/µL with 60% blasts, leading to diagnosis of SBP. After dasatinib therapy and conventional chemotherapy, he again achieved MMR. This case demonstrates that SBP may occur after achieving MMR on treatment with 2nd TKIs. Continuous careful monitoring is required for the early detection of SBP, even in patients who have achieved MMR.

Indexed as

Blast CrisisAntineoplastic Combined Chemotherapy ProtocolsDasatinibDisease ProgressionDrug Resistance, NeoplasmDrug SubstitutionEnzyme InhibitorsHumansImatinib MesylateLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMaleMiddle AgedProtein-Tyrosine KinasesPyrimidinesTreatment OutcomeDasatinibEnzyme InhibitorsImatinib MesylatenilotinibProtein-Tyrosine KinasesPyrimidinesChronic myeloid leukemiaDasatinibMajor molecular responseNilotinibSudden blast phase

Identifiers

PMID29032513
OpenAlexW2761410823

What OpenQuestion holds

Textmetadata
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.