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Efficacy and safety of frontline rituximab, cyclophosphamide, doxorubicin and prednisone plus bortezomib (VR-CAP) or vincristine (R-CHOP) in a subset of newly diagnosed mantle cell lymphoma patients medically eligible for transplantation in the randomized, phase 3 LYM-3002 study

Authors :
Drach, Johannes
Bunworasate, Udomsak
Masliak, Zvenyslava
Vilchevskaya, Kateryna
Robak, Tadeusz
Pei, Lixia
Rooney, Brendan
van de Velde, Helgi
Cavalli, Franco
Huang, Huiqiang
Samoilova, Olga
Belch, Andrew
Farber, Charles
Bosly, André
Novak, Jan
Zaucha, Jan
Dascalescu, Angela
Source :
Leukemia & Lymphoma; Apr2018, Vol. 59 Issue 4, p896-903, 8p
Publication Year :
2018

Abstract

This <italic>post-hoc</italic> subanalysis of the LYM-3002 phase 3 study assessed the efficacy and safety of substituting vincristine in rituximab, cyclophosphamide, doxorubicin and prednisone (R-CHOP; <italic>n</italic> = 42) for bortezomib (VR-CAP; <italic>n</italic> = 38) in a subgroup of 80 mantle cell lymphoma (MCL) patients aged <60 years who did not receive stem cell transplantation (SCT) despite medical eligibility. Complete response (CR)/unconfirmed CR (CRu) rates were 67 vs. 39% (odds ratio 3.69 [95% CI(confidence interval): 1.31, 10.41]; <italic>p =</italic> .012). After 40 months median follow-up, median progression-free survival by independent radiology committee with VR-CAP vs. R-CHOP was 32.6 vs. 12.0 months (hazard ratio (HR) 0.59 [95% CI: 0.31, 1.13]; <italic>p =</italic> .108); median overall survival was not reached vs. 47.3 months (HR 0.81 [95% CI: 0.33, 1.96]; <italic>p =</italic> .634). Adverse events included neutropenia (92/76%), thrombocytopenia (70/10%) and leukopenia (65/50%). VR-CAP represents a potential alternative to R-CHOP in combined and/or alternating regimens for younger, SCT-eligible MCL patients. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10428194
Volume :
59
Issue :
4
Database :
Complementary Index
Journal :
Leukemia & Lymphoma
Publication Type :
Academic Journal
Accession number :
128358906
Full Text :
https://doi.org/10.1080/10428194.2017.1365855