Evidence map›Paper›PMID 37723307›Full record

ArticleAnnals of hematology2023

Hypomethylating agents plus modified priming regimens compared with venetoclax-based regimens based on molecular characteristics for newly diagnosed patients with acute myeloid leukemia: a multi-center cohort study.

Guangyang Weng, Jingya Huang, Xin He, Tingting Xue, Linlin Yang, Yu Zhang, Guopan Yu, Zhiqiang Sun, Dongjun Lin, Lan Deng and 7 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Annals of hematology, 2023. 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
0.9field-weighted citation impact, top 22% 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, 3 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

17 authors at 9 institutions in 1 country.

Guangyang Weng *Department of Hematology, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People's Hospital, Shenzhen, China.ORCID http://orcid.org/0000-0002-7923-8972
Jingya Huang *Shenzhen Blood Center, Shenzhen, Guangdong, China.
Xin He *Department of Hematology, Zhongshan City People's Hospital, Zhongshan, China.
Tingting XueDepartment of Hematology, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People's Hospital, Shenzhen, China.
Linlin YangDepartment of Hematology, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People's Hospital, Shenzhen, China.
Yu ZhangDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Guopan YuDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Zhiqiang SunDepartment of Hematology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Dongjun LinDepartment of Hematology, the Seventh Affiliated Hospital of Sun Yat-Sen University, Shenzhen, China.
Lan DengDepartment of Hematology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Xinquan LiangDepartment of Hematology, The First People's Hospital of Chenzhou, Chenzhou, China.
Jie XiaoDepartment of Hematology, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, China.
Hongyu ZhangDepartment of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
Ziwen GuoDepartment of Hematology, Zhongshan City People's Hospital, Zhongshan, China.
Hua JinDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Qifa LiuDepartment of Hematology, Nanfang Hospital, Southern Medical University, Guangzhou, China. liuqifa628@163.com.
Xin DuDepartment of Hematology, The First Affiliated Hospital of Shenzhen University, Shenzhen Second People's Hospital, Shenzhen, China. duxingz@medmail.com.cn.
Nanfang Hospital · CNShenzhen Second People's Hospital · CNSun Yat-sen University · CNZhongshan People's Hospital · CNChenzhou First People's Hospital · CNPeking University Shenzhen Hospital · CNShanghai Jiao Tong University · CNShenzhen Blood Center · CNSouthern Medical University Shenzhen Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Venetoclax (VEN)-based regimens are the standard of care for elderly or unfit patients with newly diagnosed (ND) acute myeloid leukemia (AML). Some single-arm studies have implied that hypomethylating agents (HMAs) plus priming regimens may potentially provide an alternative therapeutic approach, owing to encouraging efficacy seen. However, no comparative data exists yet regarding these two treatment approaches. In this retrospective multi-center cohort study, we enrolled 294 ND AML patients, allocating 167 to the HMA + priming group and 127 to the VEN-based group. Treatment response and overall survival (OS) were compared between groups. Molecular subgroup analyses were also conducted. With a median of two cycles for HMA + priming group, the overall response (ORR) was 65.3%, including 55.1% complete remission (CR), 9.6% CR with incomplete hematologic recovery (CRi) and 0.6% morphologic leukemia-free state (MLFS). With a median of two cycles for VEN-based group, the ORR was 70.9%, including 46.5% CR, 18.9% CRi, and 5.5% MLFS. Response differences (ORR or CR/CRi) between groups were not significant (p > 0.05). With a median follow-up of 10.1 months, median OSs were similar between groups (20.9 vs 16.3 months, p = 0.41). However, VEN regimens demonstrated superior CR/CRi for patients with mutations in FLT3, IDH1/2, and NPM1 compared to HMA + priming (80.0% vs 35.0%, p = 0.01; 90.9% vs 65.5%, p = 0.02; 90.9% and 65.5%, p = 0.02, respectively). In conclusion, HMAs plus modified priming regimens might be a potential alternative therapeutic approach for patients with ND AML, but VEN-based regimens presented predominance in specific molecular subgroups. Molecular characteristics contribute to guiding choice of treatment.

Indexed as

Leukemia, Myeloid, AcuteAgedAntineoplastic Combined Chemotherapy ProtocolsBridged Bicyclo Compounds, HeterocyclicCohort StudiesHumansRetrospective StudiesSulfonamidesBridged Bicyclo Compounds, HeterocyclicSulfonamidesvenetoclaxAclarubicinAcute myeloid leukemiaHomoharringtonineHypomethylating agentsPriming regimensVenetoclax

Identifiers

PMID37723307
OpenAlexW4386823370

What OpenQuestion holds

Textmetadata
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.