Evidence map›Paper›PMID 26477761›Full record

ArticleZhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi2015

[Control study of melphalan instead of cyclophosphamide as a myeloablative conditioning regimen for allogeneic hematopoietic stem cell transplantation for treatment of myeloid malignancies].

Ying Zhang, Yong Huang, Jialin Wei, Zhangsong Yan, Yi He, Qiaoling Ma, Donglin Yang, Sizhou Feng, Mingzhe Han, Erlie Jiang

Open access · greenAbstract readControlled Clinical Trial
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. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

10 authors at 1 institution in 1 country.

Ying ZhangInstitute of Hematology & Blood Diseases Hospital, CAMS & PUMC, Tianjin 300020, China.
Yong HuangInstitute of Hematology & Blood Diseases Hospital, CAMS & PUMC, Tianjin 300020, China.
Jialin WeiInstitute of Hematology & Blood Diseases Hospital, CAMS & PUMC, Tianjin 300020, China.
Zhangsong YanInstitute of Hematology & Blood Diseases Hospital, CAMS & PUMC, Tianjin 300020, China.
Yi HeInstitute of Hematology & Blood Diseases Hospital, CAMS & PUMC, Tianjin 300020, China.
Qiaoling MaInstitute of Hematology & Blood Diseases Hospital, CAMS & PUMC, Tianjin 300020, China.
Donglin YangInstitute of Hematology & Blood Diseases Hospital, CAMS & PUMC, Tianjin 300020, China.
Sizhou FengInstitute of Hematology & Blood Diseases Hospital, CAMS & PUMC, Tianjin 300020, China.
Mingzhe HanInstitute of Hematology & Blood Diseases Hospital, CAMS & PUMC, Tianjin 300020, China.
Erlie JiangInstitute of Hematology & Blood Diseases Hospital, CAMS & PUMC, Tianjin 300020, China.
Institute of Hematology & Blood Diseases Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate melphalan instead of cyclophosphamide in modified busulfancyclophosphamide regimen as a new myeloablative conditioning regimen for the treatment of myeloid malignancies patients receiving allogeneic hematopoietic stem cell transplantation (HSCT).

methodsThe clinic data of 94 myeloid malignancies patients undergoing allogeneic HSCT were analyzed, of which 48 patients received Bu+Cy+Flu+Ara-C, 46 cases Bu+Mel+Flu+Ara-C regimens. Rregimen-related toxicity, engraftment, graft- versus-host disease(GVHD), infection condition, non- relapse mortality, and overall survival were compared between the two groups.

resultsAll patients achieved neutrophil engraftment. The incidence of grade Ⅲ-Ⅳ oral mucositis and diarrhea in BMFA group was higher than in BCFA group(P<0.05). The incidence of acute GVHD in BMFA group was also higher than in BCFA group but without statistically significant difference(36.5% over 56.5%, P=0.100). With a median follow up of 42 months, the incidence of no relapse mortality in BCFA group was 12.5% and 19.6% in BMFA group(P=0.400). The relapse rate in BMFA group(4.3%)was significantly lower than in BCFA group (25.0%, P=0.009). The overall survival rates were(71.8±6.7)% and(76.1±6.3)%(P=0.852), and diseasefree survival rates were(67.8±8.9)% and(76.1±6.3)%(P=0.567)were comparable between BCFA group and BMFA group.

conclusionMelphalan instead of cyclophosphamide as a new myeloablative conditioning regimen had lower relapse and satisfied disease-free survival rates, but the risk of regimenrelated toxicity and GVHD should be taken into consideration.

Indexed as

Hematopoietic Stem Cell TransplantationTransplantation ConditioningAntineoplastic Combined Chemotherapy ProtocolsCyclophosphamideDisease-Free SurvivalGraft vs Host DiseaseHematologic NeoplasmsHumansMelphalanMyeloproliferative DisordersNeoplasm Recurrence, LocalRemission InductionSurvival RateTransplantation, HomologousCyclophosphamideMelphalan

Identifiers

PMID26477761
PMCPMC7364934
OpenAlexW1800138735

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.