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Association details:
Evidence:
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

Ixazomib, dexamethasone, and rituximab in treatment-naive patients with Waldenström macroglobulinemia: long-term follow-up

Published date:
08/21/2020
Excerpt:
Fifteen patients (58%) had a CXCR4 mutation, of which 10 had nonsense mutations (5 had R338X, 4 had S338X, and 1 had G336X) and 5 had frameshift mutations (T318fs, L326fs, K327fs, S347fs, and H350fs)…. The median TTMR in patients with nonsense and frameshift CXCR4 mutations were 12 and 6 months, respectively (P = .41)....There was no detectable difference in PFS between patients with nonsense and frameshift CXCR4 mutations (P = .90). The median DOR for the 25 patients who attained a response to IDR was 38 months...
Secondary therapy:
dexamethasone
DOI:
https://doi.org/10.1182/bloodadvances.2020001963