Evidence map›Paper›PMID 27561414›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2016

Prognostic Significance of Mixed-Lineage Leukemia (MLL) Gene Detected by Real-Time Fluorescence Quantitative PCR Assay in Acute Myeloid Leukemia.

Sai Huang, Hua Yang, Yan Li, Cong Feng, Li Gao, Guo-Feng Chen, Hong-Hao Gao, Zhi Huang, Yong-Hui Li, Li Yu

Abstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  8. HighOncotarget · 2017
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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

10 authors.

Sai HuangDepartment of Hematology, Chinese PLA General Hospital, Beijing, China (mainland).
Hua YangDepartment of Hematology, Chinese PLA General Hospital, Beijing, China (mainland).
Yan LiDepartment of Hematology, Chinese PLA General Hospital, Beijing, China (mainland).
Cong FengDepartment of Emergency Medicine, Chinese PLA General Hospital, Beijing, China (mainland).
Li GaoDepartment of Hematology, China-Japan Friendship Hospital, Hepingli, Beijing, China (mainland).
Guo-Feng ChenDepartment of Hematology, Chinese PLA General Hospital, Beijing, China (mainland).
Hong-Hao GaoDepartment of Hematology, Chinese PLA General Hospital, Beijing, China (mainland).
Zhi HuangDepartment of Electrical and Computer Engineering, Indiana University-Purdue University Indianapolis, Indianapolis, IN, USA.
Yong-Hui LiDepartment of Hematology, Chinese PLA General Hospital, Beijing, China (mainland).
Li YuDepartment of Hematology, Chinese PLA General Hospital, Beijing, China (mainland).

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND The overall prognosis of acute myeloid leukemia (AML) patients with mixed-lineage leukemia (MLL) gene-positivity is unfavorable. In this study, we evaluated the expression levels of the MLL gene in AML patients. MATERIAL AND METHODS We enrolled 68 MLL gene-positive patients out of 433 newly diagnosed AML patients, and 216 bone marrow samples were collected. Real-time fluorescence quantitative PCR (RQ-PCR) was used to precisely detect the expression levels of the MLL gene. RESULTS We divided 41 patients into 2 groups according to the variation of MRD (minimal residual disease) level of the MLL gene. Group 1 (n=22) had a rapid reduction of MRD level to ≤10^-4 in all samples collected in the first 3 chemotherapy cycles, while group 2 (n=19) had MRD levels constantly >10^-4 in all samples collected in the first 3 chemotherapy cycles. Group 1 had a significantly better overall survival (p=0.001) and event-free survival (p=0.001) compared to group 2. Moreover, the patients with >10^-4 MRD level before the start of HSCT (hematopoietic stem cell transplantation) had worse prognosis and higher risk of relapse compared to patients with ≤10^-4 before the start of HSCT. CONCLUSIONS We found that a rapid reduction of MRD level to ≤10^-4 appears to be a prerequisite for better overall survival and event-free survival during the treatment of AML. The MRD levels detected by RQ-PCR were basically in line with the clinical outcome and may be of great importance in guiding early allogeneic HSCT (allo-HSCT) treatment.

Indexed as

AdolescentAdultAgedDisease-Free SurvivalFemaleFluorescenceHematopoietic Stem Cell TransplantationHistone-Lysine N-MethyltransferaseHumansLeukemia, Myeloid, AcuteMaleMiddle AgedMyeloid-Lymphoid Leukemia ProteinNeoplasm, ResidualPrognosisReal-Time Polymerase Chain ReactionHistone-Lysine N-MethyltransferaseKMT2A protein, humanMyeloid-Lymphoid Leukemia Protein

Identifiers

PMID27561414
PMCPMC5012461

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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.