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Association details:
Evidence:
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

Efficacy of assigning treatment for participants with Chronic Myelomonocytic Leukaemia based on their individual molecular results (lenzilumab plus azacitidine versus sodium ascorbate plus azacitidine).

Excerpt:
...Detection of TET2 mutation or NRAS/KRAS/CBL mutation at a variant allele frequency...
Evidence Level:
Sensitive: C2 – Inclusion Criteria
Title:

Efficacy of assigning treatment for participants with Chronic Myelomonocytic Leukaemia based on their individual molecular results (lenzilumab plus azacitidine versus sodium ascorbate plus azacitidine).

Excerpt:
...Detection of TET2 mutation or NRAS/KRAS/CBL mutation at a variant allele frequency ...
Less C2 evidence
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

1847 Lenzilumab in Addition to Azacitidine Improves Complete Response Rates in Chronic Myelomonocytic LeukemiaClinically Relevant Abstract

Published date:
11/02/2023
Excerpt:
Subjects exhibiting RAS-pathway mutations (NRAS, KRAS, CBL) receive 24 cycles (every 28 days) of AZA (SC; 75 mg/m2 for 7 days) and LENZ...Interim analysis of the PREACH-M trial demonstrated that GM-CSF neutralization with LENZ/AZA, for the treatment of CMML with RAS-pathway mutations resulted in 55% CR, achieved early in treatment, durability up to 18 months, thus far, and no unexpected serious adverse events.
Secondary therapy:
azacitidine
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

A Phase 1 Study of Lenzilumab, a humaneered recombinant Anti-Human Granulocyte-Macrophage Colony- Stimulating Factor (anti-hGM-CSF) Antibody, for Chronic Myelomonocytic Leukemia (CMML)

Published date:
11/06/2019
Excerpt:
However, 3 of 4 patients with NRAS mutation achieved clinical benefit or had clinical meaningful bone marrow myeloblast reductions.