This is something that some of our USA members have discussed with their doctors and it looks like the logic is correct.
"Patients (pts) receiving ibrutinib (ibr) for CLL rarely achieve complete remission (CR) with undetectable minimal residual disease (U-MRD). Therefore, indefinite ibr maintenance therapy (Rx) is standard of care. Long-term Rx with ibr results in a cumulative risk of Rx discontinuation due to progression or toxicity.
The risk of progression is highest in pts with complex karyotype and/or del(17p); some series suggest increased risk in pts with del(11q) or persistently elevated β2-microglobulin.
Consolidation ven added to ibr in pts with high-risk CLL was well-tolerated and achieved cumulative BM U-MRD4 rate of 73% ibr discontinuation in 49% of pts. Only 1/45 pts progressed during combination Rx. At a median of 12 mo post-ven follow up, most pts who attained BM U-MRD have ongoing U-MRD in blood. A second cohort restricted to 45 high-risk pts with TP53abnormalities or complex karyotype is accruing and there are plans to also include patients treated with acalabrutinib."
From ASH Program: Oral and Poster Abstracts Type: Oral Session: 642. Chronic Lymphocytic Leukemia: ashpublications.org/blood/a...
Jackie