Evidence map›Paper›PMID 36274263›Full record

ArticleCancer communications (London, England)2022

Optimized therapeutic strategy for patients with refractory or relapsed acute myeloid leukemia: long-term clinical outcomes and health-related quality of life assessment.

Chen-Hua Yan, Yu Wang, Yu-Qian Sun, Yi-Fei Cheng, Xiao-Dong Mo, Feng-Rong Wang, Yu-Hong Chen, Yuan-Yuan Zhang, Ting-Ting Han, Huan Chen and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer communications (London, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.7field-weighted citation impact, top 8% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Advancements in diagnosis and treatments of acute leukemia.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

14 authors at 1 institution in 2 countries.

Chen-Hua YanPeking University Peoples Hospital, Peking University Institute of Hematology, Beijing, 100044, P. R. China.
Yu WangPeking University Peoples Hospital, Peking University Institute of Hematology, Beijing, 100044, P. R. China.ORCID 0000-0003-1253-7465
Yu-Qian SunPeking University Peoples Hospital, Peking University Institute of Hematology, Beijing, 100044, P. R. China.
Yi-Fei ChengPeking University Peoples Hospital, Peking University Institute of Hematology, Beijing, 100044, P. R. China.
Xiao-Dong MoPeking University Peoples Hospital, Peking University Institute of Hematology, Beijing, 100044, P. R. China.ORCID 0000-0002-9881-7945
Feng-Rong WangPeking University Peoples Hospital, Peking University Institute of Hematology, Beijing, 100044, P. R. China.
Yu-Hong ChenPeking University Peoples Hospital, Peking University Institute of Hematology, Beijing, 100044, P. R. China.
Yuan-Yuan ZhangPeking University Peoples Hospital, Peking University Institute of Hematology, Beijing, 100044, P. R. China.
Ting-Ting HanPeking University Peoples Hospital, Peking University Institute of Hematology, Beijing, 100044, P. R. China.
Huan ChenPeking University Peoples Hospital, Peking University Institute of Hematology, Beijing, 100044, P. R. China.
Lan-Ping XuPeking University Peoples Hospital, Peking University Institute of Hematology, Beijing, 100044, P. R. China.
Xiao-Hui ZhangPeking University Peoples Hospital, Peking University Institute of Hematology, Beijing, 100044, P. R. China.
Kai-Yan LiuPeking University Peoples Hospital, Peking University Institute of Hematology, Beijing, 100044, P. R. China.
Xiao-Jun HuangPeking University Peoples Hospital, Peking University Institute of Hematology, Beijing, 100044, P. R. China.ORCID 0000-0002-2145-6643
King University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with refractory or relapsed acute myeloid leukemia (AML) have poor survival, necessitating the exploration of optimized therapeutic strategy. Here, we aimed to investigate clinical outcomes and health-related quality of life (HR-QoL) after total therapy, which included allogeneic hematopoietic stem cell transplantation (allo-HSCT), and prophylactic donor lymphocyte infusion (DLI) in the early phase after transplantation, followed by multiple measurable residual disease (MRD) and graft-versus-host disease (GvHD)-guided DLIs.

methodsConsecutive patients who had refractory or relapsed AML and had received non-T-cell-depleted allo-HSCT at Peking University Institute of Hematology were included in the study. If the patients achieved complete remission at 30 days after transplantation and had no evidence of relapse, severe infection, organ failure, and active GvHD at the time of planned DLI, prophylactic DLI was administered at 30 days after transplantation for human leukocyte antigen (HLA)-matched related HSCT or at 45-60 days after transplantation for haploidentical or unrelated HSCT. Subsequently, multiple DLIs were administered based on MRD results and whether they developed GvHD after transplantation.

resultsA total of 105 patients were eligible. Eighty-seven patients received prophylactic DLI (group B), while 18 did not receive prophylactic DLI (group A). Among 105 patients, the cumulative incidence of grade 2-4 acute GvHD and chronic GvHD was 40.6% (95% confidence interval [CI] = 30.6%-50.6%) and 73.3% (95% CI = 67.4%-79.2%), respectively. The cumulative incidence of relapse (CIR), transplant-related mortality (TRM), and leukemia-free survival (LFS) at 5 years after transplantation were 31.5% (95% CI = 21.9%-41.1%), 22.1% (95% CI = 11.3%-32.9%), and 46.4% (95% CI = 36.8%-56.0%), respectively. In group B, the CIR, TRM, and LFS at 5 years after transplantation were 27.6% (95% CI = 17.6%-37.6%), 21.6% (95% CI = 11.2%-32.0%), and 50.8% (95% CI = 40.0%-61.6%), respectively. At the end of follow-up, 48 patients survived, and more than 90% of survivors had satisfactory recoveries of HR-QoL.

conclusionsOur study indicated that total therapy is not only associated with decreased CIR, comparable TRM, and better long-term LFS, but also with satisfactory HR-QoL for refractory or relapsed AML, compared with those of standard of care therapy reported previously. Therefore, total therapy may be an optimized therapeutic strategy for refractory or relapsed AML.

Indexed as

Graft vs Host DiseaseLeukemia, Myeloid, AcuteHumansNeoplasm, ResidualQuality of LifeRecurrenceTransplantation, Homologousacute myeloid leukemiaallogeneic hematopoietic stem cell transplantationrefractoryrelapsedtotal therapy

Identifiers

PMID36274263
PMCPMC9759766
OpenAlexW4307179410

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.