Evidence map›Paper›PMID 40266290›Full record

ArticleAnnals of hematology2025

Clinical features and outcomes in large granular lymphocyte leukemia - associated pure red cell aplasia with STAT3 mutation.

Xiaoqing Liu, Xingxing Chai, Qingling Yu, Wei Wang, Qiqiang Long, Yuemin Gong, Yawen Zhang, Chun Qiao, Jianping Hao, Guangsheng He

Abstract read
In one paragraph

Article in Annals of hematology, 2025. 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
–field-weighted citation impact
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. Favorable response to second-line sirolimus regardless ofTherapeutic advances in hematology · 2026
    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

10 authors.

Xiaoqing Liu *Department of Hematology, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, 210000, China.
Xingxing Chai *Department of Hematology, The Second Lianyungang People's Hospital Affiliated to Kangda College of Nanjing Medical University, Lianyungang, 222000, China.
Qingling Yu *Department of Hematology, Affiliated Jianhu Hospital of Nantong University Xinglin College, Yancheng, 224000, China.
Wei WangDepartment of Hematology, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, 210000, China.
Qiqiang LongDepartment of Hematology, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, 210000, China.
Yuemin GongDepartment of Hematology, Jiangsu Province Hospital, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210000, China.
Yawen ZhangDepartment of Hematology, Jiangsu Province Hospital, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210000, China.
Chun QiaoDepartment of Hematology, Jiangsu Province Hospital, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210000, China.
Jianping HaoHematology Center, Xinjiang Institute of Hematology, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830000, China. 13579876416@163.com.
Guangsheng HeDepartment of Hematology, Jiangsu Province Hospital, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210000, China. heguangsheng1972@sina.com.

Funding

Research and Development Fund of Kangda College of Nanjing Medical University KD2022KYJJZD045Science and Technology Aid Project of Xinjiang Uygur Autonomous Region 2022E02132
6 · The paper itself

Abstract

Large granular lymphocyte leukemia (LGLL) is a rare lymphoproliferative disorder where somatic STAT3 mutation is common. Although LGLL has been described as an underlying condition associated with pure red cell aplasia (PRCA), the clinical characteristics and therapeutic response of LGLL - associated PRCA are largely unclear. We evaluated a set of 81 patients with LGLL - associated PRCA. Comparative analysis was performed on the clinical characteristics, responses to immunosuppressive therapy, and survival outcomes in patients with STAT3 mutation. Among the 81 LGLL - associated PRCA patients, 21 cases (26%) were STAT3 mutant, and 60 were wild - type. Of 21 patients with STAT3 mutation, 15 cases (71%) were positive for exon 21 mutation, 4 cases (19%) for exon 20 mutation, one for dual mutation in exon 20 and 21, and one for exon 13 mutation. The Y640F was the most commonly detected mutation (42.9%). Patients with STAT3 mutations had a higher percentage of reticulocytes (0.88% vs. 0.28%, P = 0.039) and red cell distribution width - coefficient of variation (18.8% vs. 15.8%, P = 0.008) compared to wild - type. Those with the STAT3 Y640F mutation had a younger median age at onset (44 years vs. 65 years, P = 0.007) and a higher peripheral blood lymphocyte ratio (63.7% vs. 34.4%, P = 0.033). The complete response rate (CRR) and overall response rate (ORR) of STAT3 mutated patients treated with cyclosporine (CsA) were 31.3% (5/16) and 56.3% (9/16), respectively, with no difference compared to the STAT3 wild - type (32.8%, 50%) (P = 0.909; P = 0.658). Although no statistical significance was found, the CRR and ORR of the CP regimen (consisted of cyclophosphamide and prednisone) were higher than CsA among STAT3 mutated individuals (53.8% vs. 31.3%, P = 0.274; 84.6% vs. 56.3%, P = 0.130). Reduction or discontinuation of immunosuppressive agents was the main cause of relapse. The relapse rate of the CP regimen was lower than CsA in this whole cohort (24.0% vs. 68.4%, P = 0.001), as well as in the STAT3 mutant group (18.2% vs. 77.8%, P = 0.022). STAT3 Y640F was the most common hotspot mutation in LGLL - associated PRCA. Patients with STAT3 mutation treated with CsA showed comparable responses to wild - type. CP regimen had a lower relapse rate and could be considered as a salvage therapy after CsA failure.

Indexed as

Leukemia, Large Granular LymphocyticMutationRed-Cell Aplasia, PureSTAT3 Transcription FactorAdultAgedAged, 80 and overFemaleHumansImmunosuppressive AgentsMaleMiddle AgedRetrospective StudiesTreatment OutcomeImmunosuppressive AgentsSTAT3 protein, humanSTAT3 Transcription FactorImmunosuppressive therapyLGLLPRCASTAT3STAT5b

Identifiers

PMID40266290
PMCPMC12053183

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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.