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Potential loss of prognostic significance of minimal residual disease assessment after R-CHOP-based induction in elderly patients with mantle cell lymphoma in the era of rituximab maintenance

. 2018 Dec ; 36 (5) : 773-778. [epub] 20180913

Language English Country England, Great Britain Media print-electronic

Document type Clinical Trial, Journal Article, Multicenter Study, Observational Study

Grant support
PROGRES Q26/LF1 Ministry of Education, Youth, and Sports
PROGRES Q28/LF1 Ministry of Education, Youth, and Sports
NPU I nr. LO1604 Ministry of Education, Youth, and Sports
AZV 17-28980A (All rights reserved) Ministry of Health of the Czech Republic
00064203 University Hospital Motol
CZ.2.16/3.1.00/24505 EU-Prague
GAUK 20214 Grant Agency of Charles University
UNCE/MED/016 Charles University Center of Excellence

Rituximab maintenance (RM) prolongs survival of elderly patients with mantle cell lymphoma (MCL). Persistent minimal residual disease (MRD) after induction repeatedly correlated with shorter progression-free survival (PFS). However, none of the published studies analyzed patients treated with RM. The main purpose was to analyze prognostic significance of MRD in the elderly patients with newly diagnosed MCL treated according to the recently published observational trial protocol (alternation of R-CHOP and R-cytarabine, 3 + 3 cycles, GovTrial number NCT03054883) at the centers that implemented RM. Minimal residual disease was evaluated by a EuroMRD standardized real-time PCR approach after 3 and 6 cycles of the induction therapy. Prognostic significance of MRD was analyzed in a subcohort of patients treated at the centers that implemented RM as a standard approach. Bone marrow proved to be a significantly more sensitive source for MRD detection than peripheral blood. In either compartment MRD (positive versus negative) after 3 or 6 cycles of the induction therapy did not correlate with PFS. The observed loss of prognostic significance of MRD after the R-CHOP-based induction appears to be a consequence of RM immune control over the residual lymphoma.

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