Evidence map›Paper›PMID 36452029›Full record

ArticleHemaSphere2022

Distinct Immunogenetic Profiles of Chronic Lymphocytic Leukemia in Asia: A Taiwan Cooperative Oncology Group Registry Study.

Chi-Yuan Yao, Andreas Agathangelidis, Shih-Sung Chuang, Hsiao-Hui Tsou, Wei-Lien Feng, Ta-Chih Liu, Tsai-Yun Chen, Yuan-Bin Yu, Su-Peng Yeh, Ming Yao and 10 more

Open access · goldAbstract read
In one paragraph

Article in HemaSphere, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. [Prognostic value of prolymphocyte percentage in chronic lymphocytic leukemia].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2025
    Article
  4. Article
  5. Review
  6. 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

20 authors at 15 institutions in 3 countries.

Chi-Yuan YaoDivision of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei City, Taiwan.
Andreas AgathangelidisDepartment of Biology, School of Science, National and Kapodistrian University of Athens, Greece.
Shih-Sung ChuangDepartment of Pathology, Chi-Mei Medical Center, Tainan City, Taiwan.
Hsiao-Hui TsouInstitute of Population Health Sciences, National Health Research Institutes, Zhunan, Miaoli County, Taiwan.
Wei-Lien FengTaiwan Cooperative Oncology Group, National Health Research Institutes, Zhunan, Miaoli County, Taiwan.
Ta-Chih LiuDepartment of Hematology-Oncology, Chang Bing Show Chwan Memorial Hospital, Changhua County, Taiwan.
Tsai-Yun ChenDepartment of Internal Medicine, Cheng-Kung University Hospital, Tainan City, Taiwan.
Yuan-Bin YuDepartment of Internal Medicine, Far-East Memorial Hospital, New Taipei City, Taiwan.
Su-Peng YehDepartment of Internal Medicine, China Medical University Hospital, Taichung City, Taiwan.
Ming YaoDivision of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei City, Taiwan.
Chuan-Cheng WangDepartment of Internal Medicine, Changhua Christian Hospital, Chuanghua County, Taiwan.
Johnson LinDepartment of Internal Medicine, Mackay Memorial Hospital, Taipei City, Taiwan.
Wen-Li HwangDepartment of Internal Medicine, Asia University Hospital, Taichung City, Taiwan.
Jyh-Pyng GauDepartment of Internal Medicine, Taipei Veterans General Hospital, Taipei City, Taiwan.
Wen-Chien ChouDivision of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei City, Taiwan.
Tsu-Yi ChaoDivision of Hematology/Oncology, Taipei Medical University-Shuang Ho Hospital, New Taipei City, Taiwan.
Liang-In LinDepartment of Clinical Laboratory Sciences and Medical Biotechnology, National Taiwan University, Taipei City, Taiwan.
Hwei-Fang TienDivision of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei City, Taiwan.
Paolo GhiaStrategic Research Program on CLL and B-cell Neoplasia Unit, Division of Experimental Oncology, Università Vita-Salute San Raffaele and IRCCS Ospedale San Raffaele, Milan, Italy.
Shang-Ju WuDivision of Hematology, Department of Internal Medicine, National Taiwan University Hospital, Taipei City, Taiwan.
National Taiwan University Hospital · TWNational Health Research Institutes · TWAsia University · TWChang Bing Show Chwan Memorial Hospital · TWChanghua Christian Hospital · TWChi Mei Medical Center · TWChina Medical University Hospital · TWFar Eastern Memorial Hospital · TWIRCCS Ospedale San Raffaele · ITMackay Memorial Hospital · TWNational and Kapodistrian University of Athens · GRNational Cheng Kung University Hospital · TWNational Taiwan University · TWTaipei Medical University-Shuang Ho Hospital · TWTaipei Veterans General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Asian patientswith chronic lymphocytic leukemia (CLL) exhibit immunoglobulin heavy variable (IGHV) gene repertoires that are distinct from those observed in Western populations, and a higher proportion of Asian CLL patients carry heavy loads of somatic hypermutations (SHM) within the B-cell receptor immunoglobulins (BcR IG). Due to the low regional incidence of CLL in Asia, only a limited number of studies had attempted to probe the phenomenon of BcR IG stereotypy in Asian populations. In this study, we analyzed the IGHV-IGHD-IGHJ gene rearrangements from a series of 255 CLL patients recruited in a nationwide, multicenter study in Taiwan. Our analysis revealed that the IGHV gene repertoire was characterized by evident biases, with IGHV3-7, IGHV4-34, and IGHV3-23 being the most frequent rearranged IGHV genes, and a higher proportion of cases carrying mutated IGHV. In terms of BcR stereotypy, the incidence of major subsets was less frequent in this cohort, with subsets #77 and #28A being the most common, while the incidence of minor subsets was approximately equivalent to that reported in the Western cohorts. With this study, we provide evidence that CLL in Asia is indeed associated with distinct immunogenetic characteristics regarding IGHV gene usage, SHM status, and BcR IG stereotypy.

Identifiers

PMID36452029
PMCPMC9704955
OpenAlexW4310144224

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.