ArticleBritish journal of haematology2026
Clonal haematopoiesis in T-follicular helper cell lymphoma: A prognostic biomarker and early event in lymphoma evolution.
Article in British journal of haematology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Clonal haematopoiesis in T-follicular helper cell lymphoma: A prognostic biomarker and early event in lymphoma evolution.British journal of haematology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
T-follicular helper cell lymphomas (TFHLs) are frequently associated with epigenetic mutations and clonal haematopoiesis (CH), but the clinical and prognostic implications of CH in TFHL remains unclear. We performed next-generation sequencing on paired peripheral blood (PB) and tumour tissue samples from 30 patients with TFHL. CH was defined by the detection of CH-associated mutations in PB at variant allele frequency ≥2%. Patients were stratified into CH-positive, CH-suspected or CH-negative based on genotyping and bone marrow involvement. CH-associated mutations were detected in PB in 12 of 30 patients (40.0%) and were suspected in four additional cases (13.3%), with no cases progressed to overt myeloid neoplasms. Ten-eleven translocation 2 and DNA methyltransferase 3A were the most frequently shared mutations between tumour and PB. CH-positive patients were significantly older, exhibited poorer performance status (Eastern Cooperative Oncology Group [ECOG] ≥2: 50.0% vs. 0.0%, p = 0.004), elevated systemic inflammation (high-sensitivity C-reactive protein [hs-CRP]: 66.9 vs. 20.3 mg/L, p = 0.010) and inferior treatment response (complete response [CR] rate: 9.1% vs. 50.0%, p = 0.042). In multivariate analysis adjusting for age and ECOG performance status, CH positivity remained independently associated with inferior progression-free survival (PFS) (hazard ratio [HR] = 4.41, 95% confidence interval [CI]: 1.46-13.35, p = 0.009), even after adjustment for age and ECOG performance status. In conclusions, CH is common in TFHL which represents early events in lymphomagenesis and is associated with elevated systemic inflammation, poor performance status, worse treatment response and inferior PFS.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.