Evidence map›Paper›PMID 39622998›Full record

ArticleBone marrow transplantation2025

Outcomes of allogeneic hematopoietic stem cell transplantation versus intensive chemotherapy in patients with myeloid sarcoma: a nationwide representative multicenter study.

Jie Sun, Yi-Cheng Zhang, Jia Wei, Ya-Jing Xu, Yue Zhang, Yu-Hua Li, An-Qin Wu, Lei Fan, Yu Zhu, Feng-Qi Liu and 17 more

Abstract readMulticenter StudyComparative Study
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

  1. [A case of isolated myeloid sarcoma initially presenting as a mediastinal mass].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2026
    Article
  2. Article
  3. Review
  4. Diagnostic Approaches in Myeloid Sarcoma.Current issues in molecular biology · 2025
    Review
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

27 authors.

Jie Sun *Peking University People's Hospital, Peking University Institute of Hematology, Beijing, China.ORCID 0000-0002-8568-6472
Yi-Cheng Zhang *Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Jia WeiDepartment of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.ORCID 0000-0002-6435-9368
Ya-Jing XuDepartment of Hematology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yue ZhangDepartment of Hematology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yu-Hua LiDepartment of Hematology, Zhujiang Hospital of Southern Medical University, Guangzhou, Guangdong, China.ORCID 0000-0001-7174-0338
An-Qin WuDepartment of Hematology, Zhujiang Hospital of Southern Medical University, Guangzhou, Guangdong, China.
Lei FanDepartment of Hematology, Jiangsu Province Hospital, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Yu ZhuDepartment of Hematology, Jiangsu Province Hospital, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Feng-Qi LiuDepartment of Hematology, Jiangsu Province Hospital, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Zhong-Xing JiangDepartment of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Chao LiuDepartment of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Ming JiangDepartment of Hematology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang Uygur Autonomous Region, China.
Jian-Hua QuDepartment of Hematology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang Uygur Autonomous Region, China.
Peng-Cheng HeDepartment of Hematology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Jie WangDepartment of Hematology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Xiao-Bing HuangDepartment of Hematology, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.ORCID 0009-0001-2083-7663
Rong XiaoDepartment of Hematology, Sichuan Academy of Medical Sciences and Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, Sichuan, China.
Su-Jun GaoDepartment of Hematology, The First Hospital of Jilin University, Changchun, Jilin, China.
Qiang GuoDepartment of Hematology, The First Hospital of Jilin University, Changchun, Jilin, China.
San-Bin WangDepartment of Hematology, 920th Hospital of Joint Logistics Support Force, Kunming, Yunnan, China.
Xiao-Ping LiDepartment of Hematology, 920th Hospital of Joint Logistics Support Force, Kunming, Yunnan, China.
Sheng-Jin FanDepartment of Hematology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Li-Li SunDepartment of Hematology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Lan-Ping XuPeking University People's Hospital, Peking University Institute of Hematology, Beijing, China.
Xiao-Jun HuangPeking University People's Hospital, Peking University Institute of Hematology, Beijing, China.
Xiao-Hui ZhangPeking University People's Hospital, Peking University Institute of Hematology, Beijing, China. zhangxh@bjmu.edu.cn.ORCID 0000-0003-4730-256X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myeloid sarcoma (MS) is a rare hematological neoplasm with poor prognosis, posing a significant clinical challenge due to the absence of effective and standardized treatments. We conducted a retrospective analysis of 162 MS patients treated at 12 centers to compare outcomes between intensive chemotherapy and allogeneic hematopoietic stem cell transplantation (allo-HSCT). Our analysis revealed that allo-HSCT demonstrated superior overall survival (OS) within the initial 36 months compared to intensive chemotherapy alone (p = 0.037). However, beyond 36 months (36-60 months), a reverse trend was observed (p = 0.056). Subgroup analysis revealed potential benefit for isolated MS patients with allo-HSCT, but not for those with leukemic MS. Additionally, in patients achieving first complete remission (CR1) after induction chemotherapy, allo-HSCT did not significantly improve 5-year OS compared with intensive chemotherapy alone (p = 0.25). Conversely, allo-HSCT significantly improved 5-year OS in non-CR1 patients (p < 0.001). Notably, HLA-matched HSCT and haploidentical HSCT showed comparable outcomes in terms of OS, disease-free survival, and cumulative incidence of relapse. In conclusion, allo-HSCT improved outcomes for MS patients within 36 months of disease onset, and haploidentical HSCT emerged as a viable treatment option for patients without matched donors.

Indexed as

Hematopoietic Stem Cell TransplantationSarcoma, MyeloidAdolescentAdultAgedAllograftsDisease-Free SurvivalFemaleHumansMaleMiddle AgedRetrospective StudiesSurvival RateTransplantation, HomologousTreatment OutcomeYoung Adult

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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.