# CD34-positive circulating cells quantification during follow-up in myeloproliferative neoplasms

**Authors:** Marine Demoy, Maxence Bauvais, Agathe Vely, Thomas Nicol, Jérémie Riou, Hortense Le Jeanne, Aurélien Bauduin, Hubert Rambaud, Françoise Boyer, Franck Geneviève, Agathe Boussaroque, Marie-Christine Copin, Valérie Ugo, Corentin Orvain, Damien Luque Paz

PMC · DOI: 10.1007/s00277-026-06755-1 · Annals of Hematology · 2026-01-16

## TL;DR

Tracking CD34-positive cells in blood helps predict disease progression and survival in patients with myeloproliferative neoplasms.

## Contribution

The study demonstrates that serial CD34-positive cell counts are useful for monitoring progression and prognosis in myeloproliferative neoplasms.

## Key findings

- CD34-positive cell counts with a threshold of 15/µL effectively diagnose post-ET/PV myelofibrosis with high specificity and NPV.
- Lower CD34-positive cell levels correlate with treatment response in myelofibrosis patients.
- Higher CD34-positive cell counts (≥100/µL) are independently linked to increased mortality in myelofibrosis.

## Abstract

Polycythemia vera (PV) and Essential thrombcythemia (ET) are myeloproliferative neoplasms (MPNs) that can progress to secondary myelofibrosis, a complication associated with increased mortality. Circulating CD34-positive cells at diagnosis can be used to distinguish primary myelofibrosis from other MPNs with a threshold of 10/µL. In this study, we evaluate the interest of serial CD34-positive cell quantifications during the follow-up of MPNs. We retrospectively include 180 patients with MPN (90 ET, 55 PV and 35 myelofibrosis) with at least two measurements of circulating CD34-positive cells. CD34-positive cell count showed an AUC of 0.901 for the diagnosis of post-ET/PV myelofibrosis, with a sensitivity of 54.8%, a specificity of 99.5%, a PPV of 89.5% and a NPV of 96.3% for the threshold of 15 cells/µL. The decreased sensibility could be explained by an impact of cytoreductive treatments. Then we focused on primary and secondary myelofibrosis (MF) and found that patients achieving partial or complete response (per IWG-MRT criteria) had lower CD34-positive cell levels. Finally, CD34-positive cell levels had a prognostic impact on overall survival in MF, a count ≥ 100/µL is predictive of a higher risk of death (HR = 2.9 [1.5–5.9]), independently of DIPSS classification. In conclusion, monitoring of circulating CD34-positive cells is valuable for evaluating both disease progression and prognosis in MPN patients.

The online version contains supplementary material available at 10.1007/s00277-026-06755-1.

## Linked entities

- **Proteins:** CD34 (CD34 molecule)
- **Diseases:** Polycythemia vera (MONDO:0009891), Essential thrombocytemia (MONDO:0005029), myeloproliferative neoplasms (MONDO:0020076), myelofibrosis (MONDO:0044903)

## Full-text entities

- **Genes:** MPL (MPL proto-oncogene, thrombopoietin receptor) [NCBI Gene 4352] {aka C-MPL, CD110, MPLV, THCYT2, THPOR, TPOR}, CLEC3B (C-type lectin domain family 3 member B) [NCBI Gene 7123] {aka MCDR4, TN, TNA}, CALR (calreticulin) [NCBI Gene 811] {aka CALR1, CRT, HEL-S-99n, RO, SSA, cC1qR}, CD34 (CD34 molecule) [NCBI Gene 947], JAK2 (Janus kinase 2) [NCBI Gene 3717] {aka JTK10}, MDM2 (MDM2 proto-oncogene) [NCBI Gene 4193] {aka ACTFS, HDMX, LSKB, hdm2}, ABL1 (ABL proto-oncogene 1, non-receptor tyrosine kinase) [NCBI Gene 25] {aka ABL, BCR-ABL, CHDSKM, JTK7, bcr/abl, c-ABL}
- **Diseases:** chronic myeloid disorders (MESH:D015464), vascular complications (MESH:D003925), MDS (MESH:D009190), death (MESH:D003643), AML (MESH:D015470), MF (MESH:D055728), CMML (MESH:D054429), PV (MESH:D011087), essential thrombocythemia (MESH:D013920), haematological disorders (MESH:D006402), aplasia (MESH:C536482), acute myeloid leukaemia (MESH:D054218), thrombosis (MESH:D013927), fibrosis (MESH:D005355), MPNs (MESH:D009369), chronic myelomonocytic leukaemia (MESH:D015477), DIPSS (MESH:D000082122), ET (MESH:D020329)
- **Chemicals:** EDTA (MESH:D004492), Ruxolitinib (MESH:C540383), anagrelide (MESH:C021139), 7-AAD (MESH:C025942), navtemadlin (MESH:C588087), alpha-pegylated interferon (-), hydroxyurea (MESH:D006918)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** AUC of 0, W515L

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12808151