Evidence map›Paper›PMID 25501350›Full record

ArticleBone marrow transplantation2015

Impact of IKZF1 deletions on long-term outcomes of allo-SCT following imatinib-based chemotherapy in adult Philadelphia chromosome-positive ALL.

M Kim, J Park, D-W Kim, Y-J Kim, Y-W Jeon, J-H Yoon, S-H Shin, S-A Yahng, S-E Lee, B-S Cho and 9 more

Abstract read
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In one paragraph

Article in Bone marrow transplantation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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  8. Observational
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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

19 authors at 1 institution in 1 country.

M KimDepartment of Laboratory Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.
J ParkDepartment of Laboratory Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.
D-W KimDepartment of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Y-J KimDepartment of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Y-W JeonDepartment of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
J-H YoonDepartment of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
S-H ShinDepartment of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
S-A YahngDepartment of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
S-E LeeDepartment of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
B-S ChoDepartment of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
K-S EomDepartment of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
H-J KimDepartment of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
C-Ki MinDepartment of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
S-G ChoDepartment of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Y KimDepartment of Laboratory Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.
J-W LeeDepartment of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
K HanDepartment of Laboratory Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.
W-S MinDepartment of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
S LeeDepartment of Hematology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Catholic University of Korea · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We investigated the prognostic relevance of IKZF1 deletions in 118 adult Ph-positive ALL patients who had minimal residual disease (MRD) data under a uniform treatment of allo-SCT following first-line imatinib-based chemotherapy. IKZF1 deletions were identified in 93 patients (78.8%). IKZF1-deleted patients had a lower proportion of early-stable molecular responders compared with wild-type patients (28.0 vs 56.0%, P=0.028). After a median follow-up of 72 months, IKZF1-deleted patients had a trend for higher cumulative incidence of relapse (CIR) (38.0 vs 13.3%, P=0.052), particularly in a subgroup of early-stable molecular responders (n=40; 21.4 vs 0%, P=0.088), but comparable disease-free survival to wild-type patients. Patients with biallelic-null deletions showed higher CIR (74.6 vs 13.3%, P=0.003) and lower disease-free survival (20.0 vs 67.5%, P=0.022) than wild-type patients. In multivariate analysis, MRD kinetics were closely related to outcomes, while neither IKZF1 deletions nor their functional subtypes retained an independent statistical power. Within the limitation of sample size, however, considering both the negative impact of IKZF1 deletions on MRD kinetics and a trend for relationship between IKZF1 deletions and relapse in early-stable molecular responders, IKZF1 deletions may have a potentially additive effect on unfavorable prognosis in a specific MRD-based subgroup of adult Ph-positive ALL transplants.

Indexed as

AdolescentAdultAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsBenzamidesFemaleHumansIkaros Transcription FactorImatinib MesylateMaleMiddle AgedPiperazinesPrecursor Cell Lymphoblastic Leukemia-LymphomaPyrimidinesSequence DeletionTreatment OutcomeAntineoplastic AgentsBenzamidesIkaros Transcription FactorIKZF1 protein, humanImatinib MesylatePiperazinesPyrimidines

Identifiers

PMID25501350
OpenAlexW2069702102

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Registered trials

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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.