Allele burden thresholds
Current understanding
JAK2 V617F allele burden as a transplant eligibility and outcome predictor — emerging evidence on optimal cutoffs.
Evidence log
- 2026-10-07 — Outcome heterogeneity in CALR-mutated myeloproliferative neoplasms.: Extends the serial-monitoring argument from CALR allele burden alone to broader serial NGS profiling, since acquired TP53/KRAS/RUNX1 co-mutations — not CALR burden — drive the transplant-timing decision in CALR-mutated MPN. (novelty: 3)
- 2026-06-23 — A Pragmatic Clinical Trial to Prevent Relapse for Myeloid Malignancies With Measurable Disease Prior to Allogeneic Transplant: MRD-guided maintenance trial operationalizes pre-/post-transplant residual disease measurement as the trigger for treatment assignment — extends allele-burden/MRD thresholds from a prognostic marker into an actionable decision rule for post-HCT therapy. (novelty: 3)
- 2026-03-06 — Interest of CALR Allele Burden in Diagnosis and Follow-up of Patients With CALR Mutated Myeloproliferative Syndromes (CALRSUIVI): CALRSUIVI prospective observational study evaluates CALR allele burden as a molecular marker for disease progression and follow-up in CALR-mutated MPN, extending the allele-burden-monitoring paradigm beyond JAK2 V617F — though direct linkage to transplant timing/eligibility thresholds remains to be established. (novelty: 3)
Open questions
Related
Contributing findings
Outcome heterogeneity in CALR-mutated myeloproliferative neoplasms.
07-oct-2026
novelty 3
per-area 2
mentions
A Pragmatic Clinical Trial to Prevent Relapse for Myeloid Malignancies With Measurable Disease Prior to Allogeneic Transplant
23-jun-2026
novelty 3
per-area 3
strengthens
[Allogeneic haematopoietic stem cell transplantation in myelofibrosis: Patient selection, pre-transplant preparation and harmonisation of practices (SFGM-TC)].
17-jun-2026
novelty 2
per-area 2
mentions
Allogeneic Transplantation in the Rare Disease Myelodysplastic Syndrome/Myeloproliferative Neoplasm with Neutrophilia: Age and Disease Burden Determine Outcome.
16-jun-2026
novelty 3
per-area 2
mentions
Calreticulin mutations in essential thrombocythemia and primary myelofibrosis.
01-jun-2026
novelty 2
per-area 2
strengthens
Interest of CALR Allele Burden in Diagnosis and Follow-up of Patients With CALR Mutated Myeloproliferative Syndromes (CALRSUIVI)
06-mar-2026
novelty 3
per-area 3
strengthens