Evidence map›Paper›PMID 29232940›Full record

ArticleThe Korean journal of internal medicine2018

No benefit of hypomethylating agents compared to supportive care for higher risk myelodysplastic syndrome.

Sang Kyun Sohn, Joon Ho Moon, In Hee Lee, Jae Sook Ahn, Hyeoung Joon Kim, Joo Seop Chung, Ho Jin Shin, Sung Woo Park, Won Sik Lee, Sang Min Lee and 10 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in The Korean journal of internal medicine, 2018. 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 42% 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. 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

20 authors at 9 institutions in 1 country.

Sang Kyun SohnDepartment of Hematology/Oncology, Kyungpook National University Hospital, Daegu, Korea.
Joon Ho MoonDepartment of Hematology/Oncology, Kyungpook National University Hospital, Daegu, Korea.
In Hee LeeDepartment of Hematology/Oncology, Kyungpook National University Hospital, Daegu, Korea.
Jae Sook AhnDepartment of Hematology/Oncology, Chonnam National University Hwasun Hospital, Hwasun, Korea.
Hyeoung Joon KimDepartment of Hematology/Oncology, Chonnam National University Hwasun Hospital, Hwasun, Korea.
Joo Seop ChungDepartment of Hematology/Oncology, Pusan National University Hospital, Busan, Korea.
Ho Jin ShinDepartment of Hematology/Oncology, Pusan National University Hospital, Busan, Korea.
Sung Woo ParkDepartment of Hematology/Oncology, Pusan National University Hospital, Busan, Korea.
Won Sik LeeDepartment of Hematology/Oncology, Inje University Busan Baik Hospital, Busan, Korea.
Sang Min LeeDepartment of Hematology/Oncology, Inje University Busan Baik Hospital, Busan, Korea.
Hawk KimDepartment of Hematology/Oncology, Ulsan University Hospital, Ulsan, Korea.
Ho Sup LeeDepartment of Hematology/Oncology, Kosin University Gospel Hospital, Busan, Korea.
Yang Soo KimDepartment of Hematology/Oncology, Kosin University Gospel Hospital, Busan, Korea.
Yoon Young ChoDepartment of Hematology/Oncology, Daegu Catholic University Medical Center, Daegu, Korea.
Sung Hwa BaeDepartment of Hematology/Oncology, Daegu Catholic University Medical Center, Daegu, Korea.
Ji Hyun LeeDepartment of Hematology/Oncology, Dong-A University Hospital, Busan, Korea.
Sung Hyun KimDepartment of Hematology/Oncology, Dong-A University Hospital, Busan, Korea.
Ik Chan SongDepartment of Hematology/Oncology, Chungnam National University Hospital, Daejeon, Korea.
Ji Hyun KwonDepartment of Hematology/Oncology, Chungbuk National University Hospital, Cheongju, Korea.
Yoo Jin LeeDepartment of Hematology/Oncology, Kyungpook National University Hospital, Daegu, Korea.
Kyungpook National University Hospital · KRChonnam National University Hwasun Hospital · KRPusan National University Hospital · KRDaegu Catholic University Medical Center · KRDong-A University Hospital · KRInje University Busan Paik Hospital · KRKosin University Gospel Hospital · KRChungbuk National University Hospital · KRChungnam National University Hospital · KR

Funding

Kyungpook National University Research Fund
6 · The paper itself

Abstract

BACKGROUND/

aimsThis study evaluated the role of hypomethylating agents (HMA) compared to best supportive care (BSC) for patients with high or very-high (H/VH) risk myelodysplastic syndrome (MDS) according to the Revised International Prognostic Scoring System.

methodsA total of 279 H/VH risk MDS patients registered in the Korean MDS Working Party database were retrospectively analyzed.

resultsHMA therapy was administered to 205 patients (73.5%), including 31 patients (11.1%) who then received allogeneic hematopoietic cell transplantation (allo-HCT), while 74 patients (26.5%) received BSC or allo-HCT without HMA. The 3-year overall survival (OS) rates were 53.1% ± 10.7% for allo-HCT with HMA, 75% ± 21.7% for allo-HCT without HMA, 17.3% ± 3.6% for HMA, and 20.8% ± 6.9% for BSC groups (p < 0.001). In the multivariate analysis, only allo-HCT was related with favorable OS (hazard ratio [HR], 0.356; p = 0.002), while very poor cytogenetic risk (HR, 5.696; p = 0.042), age ≥ 65 years (HR, 1.578; p = 0.022), Eastern Cooperative Oncology Group performance status (ECOG PS) 2 to 4 (HR, 2.837; p < 0.001), and transformation to acute myeloid leukemia (AML) (HR, 1.901; p = 0.001) all had an adverse effect on OS.

conclusionFor the H/VH risk group, very poor cytogenetic risk, age ≥ 65 years, ECOG PS 2 to 4, and AML transformation were poor prognostic factors. HMA showed no benefit in terms of OS when compared to BSC. Allo-HCT was the only factor predicting a favorable long-term outcome. The use of HMA therapy did not seem to have an adverse effect on the transplantation outcomes. However, the conclusion of this study should be carefully interpreted and proven by large scale research in the future.

Indexed as

Hematopoietic Stem Cell TransplantationAdolescentAdultAgedAged, 80 and overAzacitidineDatabases, FactualDecitabineDisease ProgressionDNA MethylationDNA Modification MethylasesEnzyme InhibitorsFemaleHumansMaleMiddle AgedAzacitidineDecitabineDNA Modification MethylasesEnzyme InhibitorsHigher riskHypomethylating agentMyelodysplasiaRevised International Prognostic Scoring System

Identifiers

PMID29232940
PMCPMC6234402
OpenAlexW2775125201

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.