Evidence map›Paper›PMID 28910431›Full record

ArticleJAMA oncology2018

HLA-Mismatched Microtransplant in Older Patients Newly Diagnosed With Acute Myeloid Leukemia: Results From the Microtransplantation Interest Group.

Mei Guo, Nelson J Chao, Jian-Yong Li, David A Rizzieri, Qi-Yun Sun, Ann Mohrbacher, Elizabeth F Krakow, Wan-Jun Sun, Xu-Liang Shen, Xin-Rong Zhan and 25 more

Open access · bronzeAbstract readClinical StudyMulticenter Study
In one paragraph

Article in JAMA oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 47 citations in OpenAlex.

  1. Trial
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  4. Predictive risk model of mild cognitive impairment in patients with malignant haematological diseases after haematopoietic stem cell transplantation.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025
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  9. Harnessing allogeneic CD4Fukushima journal of medical science · 2023
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  17. Alloantigen-activated (AAA) CD4Journal of experimental & clinical cancer research : CR · 2021
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

35 authors at 16 institutions in 3 countries.

Mei GuoDepartment of Hematology and Transplantation, Affiliated Hospital of The Academy of Military Medical Sciences, Beijing, China.
Nelson J ChaoDivision of Hematologic Malignancies and Cellular Therapy, Department of Medicine, Duke University, Duke Cancer Institute, Durham, North Carolina.
Jian-Yong LiDepartment of Hematology, Jiangsu Province People's Hospital, Nanjing, China.
David A RizzieriDivision of Hematologic Malignancies and Cellular Therapy, Department of Medicine, Duke University, Duke Cancer Institute, Durham, North Carolina.
Qi-Yun SunDepartment of Hematology and Transplantation, Affiliated Hospital of The Academy of Military Medical Sciences, Beijing, China.
Ann MohrbacherJane Anne Nohl Division of Hematology and Center for the Study of Blood Diseases, Keck School of Medicine of University of Southern California, Los Angeles.
Elizabeth F KrakowDivision of Medical Oncology, University of Washington, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle.
Wan-Jun SunDepartment of Hematology, The Second Artillery General Hospital, Beijing, China.
Xu-Liang ShenDepartment of Hematology, He Ping Central Hospital of the Changzhi Medical College, Changzhi, China.
Xin-Rong ZhanDepartment of Hematology, Central Hospital of Xinxiang City, Xinxiang, China.
De-Pei WuDepartment of Hematology, The First Affiliated Hospital of Soochow University, Suzhou, China.
Li LiuDepartment of Hematology, The Fourth Military Medical University, Xi'an, China.
Juan WangDepartment of Hematology, Central Hospital of Cangzhou City, Cangzhou, China.
Min ZhouDepartment of Hematology, The Second People's Hospital of Changzhou City, Changzhou, China.
Lin-Hua YangDepartment of Hematology, The Second Affiliated Hospital of Shanxi University, Taiyuan, China.
Yang-Yi BaoDepartment of Hematology, Central Hospital of Hefei City, Hefei, China.
Zheng DongDepartment of Hematology and Transplantation, Affiliated Hospital of The Academy of Military Medical Sciences, Beijing, China.
Bo CaiDepartment of Hematology and Transplantation, Affiliated Hospital of The Academy of Military Medical Sciences, Beijing, China.
Kai-Xun HuDepartment of Hematology and Transplantation, Affiliated Hospital of The Academy of Military Medical Sciences, Beijing, China.
Chang-Lin YuDepartment of Hematology and Transplantation, Affiliated Hospital of The Academy of Military Medical Sciences, Beijing, China.
Jian-Hui QiaoDepartment of Hematology and Transplantation, Affiliated Hospital of The Academy of Military Medical Sciences, Beijing, China.
Hong-Li ZuoDepartment of Hematology and Transplantation, Affiliated Hospital of The Academy of Military Medical Sciences, Beijing, China.
Ya-Jing HuangDepartment of Hematology and Transplantation, Affiliated Hospital of The Academy of Military Medical Sciences, Beijing, China.
Anthony D SungDivision of Hematologic Malignancies and Cellular Therapy, Department of Medicine, Duke University, Duke Cancer Institute, Durham, North Carolina.
Jun-Xiao QiaoDepartment of Hematology, The Second Artillery General Hospital, Beijing, China.
Zhi-Qing LiuDepartment of Hematology and Transplantation, Affiliated Hospital of The Academy of Military Medical Sciences, Beijing, China.
Tie-Qiang LiuDepartment of Hematology and Transplantation, Affiliated Hospital of The Academy of Military Medical Sciences, Beijing, China.
Bo YaoDepartment of Hematology and Transplantation, Affiliated Hospital of The Academy of Military Medical Sciences, Beijing, China.
Hong-Xia ZhaoDepartment of Hematology, The Second Artillery General Hospital, Beijing, China.
Si-Xuan QianDepartment of Hematology, Jiangsu Province People's Hospital, Nanjing, China.
Wei-Wei LiuStatistics Department, The Academy of Military Medical Sciences, Beijing, China.
Rafael ForésDepartment of Hematology, Hospital Universitario Puerta de Hierro, Majadahonda, Comunidad de Madrid, Spain.
Rafael F DuarteDepartment of Hematology, Hospital Universitario Puerta de Hierro, Majadahonda, Comunidad de Madrid, Spain.
Hui-Sheng AiDepartment of Hematology and Transplantation, Affiliated Hospital of The Academy of Military Medical Sciences, Beijing, China.
Microtransplantation Interest Group
Academy of Military Medical Sciences · CNSecond Artillery General Hospital of Chinese People's Liberation Army · CNDuke University · USAir Force Medical University · CNCangzhou Central Hospital · CNChangzhi Medical College · CNComunidad de Madrid · ESDuke Cancer InstituteFirst Affiliated Hospital of Soochow University · CNFourth People's Hospital of Changzhou · CNFred Hutch Cancer Center · USHefei First People's Hospital · CNHospital Universitario Puerta de Hierro Majadahonda · ESShanxi University · CNUniversity of Southern California · USXinxiang Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

importanceThe outcome of older patients with acute myeloid leukemia (AML) remains unsatisfactory. Recent studies have shown that HLA-mismatched microtransplant could improve outcomes in such patients.

objectiveTo evaluate outcomes in different age groups among older patients with newly diagnosed AML who receive HLA-mismatched microtransplant. DESIGN, SETTING, AND

participantsThis multicenter clinical study included 185 patients with de novo AML at 12 centers in China, the United States, and Spain in the Microtransplantation Interest Group. Patients were divided into the following 4 age groups: 60 to 64 years, 65 to 69 years, 70 to 74 years, and 75 to 85 years. The study period was May 1, 2006, to July 31, 2015. EXPOSURES: Induction chemotherapy and postremission therapy with cytarabine hydrochloride with or without anthracycline, followed by highly HLA-mismatched related or fully mismatched unrelated donor cell infusion. No graft-vs-host disease prophylaxis was used. MAIN OUTCOMES AND MEASURES: The primary end point of the study was to evaluate the complete remission rates, leukemia-free survival, and overall survival in different age groups. Additional end points of the study included hematopoietic recovery, graft-vs-host disease, relapse rate, nonrelapse mortality, and other treatment-related toxicities.

resultsAmong 185 patients, the median age was 67 years (range, 60-85 years), and 75 (40.5%) were female. The denominators in adjusted percentages in overall survival, leukemia-free survival, relapse, and nonrelapse mortality are not the sample proportions of observations. The overall complete remission rate was not significantly different among the 4 age groups (75.4% [52 of 69], 70.2% [33 of 47], 79.1% [34 of 43], and 73.1% [19 of 26). The 1-year overall survival rates were 87.7%, 85.8%, and 77.8% in the first 3 age groups, which were much higher than the rate in the fourth age group (51.7%) (P = .004, P = .008, and P = .04, respectively). The 2-year overall survival rates were 63.7% and 66.8% in the first 2 age groups, which were higher than the rates in the last 2 age groups (34.2% and 14.8%) (P = .02, P = .03, P < .001, and P < .001, respectively). The 1-year cumulative incidences of nonrelapse mortality were 10.2%, 0%, 3.4%, and 26.0% in the 4 age groups and 8.1% in all patients. The median times to neutrophil and platelet recovery were 12 days and 14 days after induction chemotherapy, respectively. Five patients had full or mixed donor engraftment, and 30.8% (8 of 26) of patients demonstrated donor microchimerism. Two patients (1.1%) developed severe acute graft-vs-host disease. CONCLUSIONS AND RELEVANCE: Microtransplant achieved a high complete remission rate in AML patients aged 60 to 85 years and higher 1-year overall survival in those aged 60 to 74 years.

Indexed as

AgingAgedAged, 80 and overAge of OnsetAllograftsChinaFemaleGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHistocompatibility TestingHumansLeukemia, Myeloid, AcuteMaleMiddle AgedRemission InductionSpain

Identifiers

PMID28910431
PMCPMC5833633
OpenAlexW2756086179

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