Evidence map›Paper›PMID 26134011›Full record

ArticleZhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi2015

[Combination of busulfan with increased-dose of fludarabine as conditioning regimen for MDS and MDS-AML patients with allo-HSCT].

Jing Yuan, Hanyun Ren, Zhixiang Qiu, Yuan Li, Mangju Wang, Wei Liu, Weilin Xu, Yuhua Sun, Lihong Wang, Zeyin Liang and 6 more

Open access · greenAbstract read
In one paragraph

Article in Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 2015. 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
0.2field-weighted citation impact, top 39% 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, 2 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

16 authors at 1 institution in 1 country.

Jing YuanDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Hanyun RenDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Zhixiang QiuDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Yuan LiDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Mangju WangDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Wei LiuDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Weilin XuDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Yuhua SunDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Lihong WangDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Zeyin LiangDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Yujun DongDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Jinping OuDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Wensheng WangDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Yue YinDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Xinan CenDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Qian WangDepartment of Hematology, Peking University First Hospital, Beijing 100034, China.
Peking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo investigate the safety and efficacy of allogeneic hematopoietic stem cell transplantation (allo-HSCT) for myelodysplastic syndrome (MDS) and secondary acute myelogenous leukemia (MDS-AML) using conditioning regimen with busulfan (Bu) and increased-dose of fludarabine (ID-Flu).

methodsA total of 49 patients with MDS or MDS-AML were treated by allo-HSCT, the clinical data was analyzed retrospectively.

resultsAll patients achieved hematopoietic reconstitution. Neutrophil engraftment was at 10 - 22 days (median 13 days), and platelet engraftment was at 8 - 66 days (median 16 days). The cumulative incidences of Ⅱ-Ⅳ degree acute graft-versus-host disease (GVHD), hemorrhagic cystitis (HC), and hepatic venous occlusive disease (VOD) were 28.6%, 14.3% and 2.0%, respectively. The transplant-related mortality (TRM) was only 4.1% at 100d and 8.2% at 1-92 months of followed-up (median 14 months) period. Overall survival (OS) and disease free survival (DFS) was 75.5%, 73.5%, respectively. Kaplan-Meier curve showed that 3-year OS and 3-year DFS was (71.1 ± 7.8)%, (66.7 ± 8.3)%, respectively, with a relapse incidence (RI) 16.3%. OS for MDS and MDS-AML was 81.5% and 68.2%, and RI in two settings was 3.7%, 31.8%, respectively. OS for MDS-AML at complete remission (CR) and non-CR subgroup was 83.3% and 50.0%, respectively, while cumulative RR was 16.7% and 50.0%, respectively. OS and RI except for non-CR subgroup were 82.1% and 7.7%. Univariate analysis showed that pre-HSCT disease status had correlation with OS (P=0.031), but age, decitabine in conditioning regimen, stem cell source, HLA matching, patient-donor gender, dose of mononuclear cells and GVHD had no correlation with OS.

conclusionBu/ID-Flu conditioning regimen for MDS and MDS-AML has high efficiency, fewer complications, lower toxicity and TRM. The OS and DFS were higher and RI was lower except for refractory MDS-AML patients. The regimen is valuable for clinical application.

Indexed as

Leukemia, Myeloid, AcuteMyelodysplastic SyndromesBusulfanDisease-Free SurvivalGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansRecurrenceRemission InductionRetrospective StudiesTissue DonorsTransplantation ConditioningTransplantation, HomologousVidarabineBusulfanfludarabineVidarabine

Identifiers

PMID26134011
PMCPMC7343060
OpenAlexW2460798730

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.