Combination therapy for the treatment of leukemia

Share This Post

Venetoclax (Venclexta) and rituximab (Rituxan) are used in combination with relapsed refractory chronic lymphocytic leukemia ( CLL ), resulting in a high rate of undetectable minimal residual disease ( uMRD ), which is associated with prolonged progression-free survival ( PFS ).

Venetoclax and rituximab-treated patients had almost 5 times the uMRD status as combined with phenytoin and rituximab , and the proportion of patients who maintained this status at 24 months was higher in the venetoclax / rituximab group the 20 or more times. Compared with MRD- positive status, uMRD was associated with a 62 % reduction in risk of disease progression or death .

The MRD status has been proven to predict PFS in CLL patients treated with chemoimmunotherapy , but the predictive value of MRD for new drugs remains uncertain. Data from the random MURANO trial provides an opportunity to examine the predictive value of MRD and CLL without chemotherapy.

MURANO is a phase III randomized trial evaluating the efficacy of rituximab combined with venetoclax versus bendamustine in 389 patients with relapsed / refractory CLL . The patient received 2 years of venetoclax and the first 6 months of rituximab, or 6 months of bendamustine plus rituximab for 6 months.

Preliminary analysis showed that compared with rituximab and bendamustine, the risk of disease progression or death was 84% at 3 years of treatment with venetoclax and rituximab.

Subscribe To Our Newsletter

Get updates and never miss a blog from Cancerfax

More To Explore

Targeting FGFR4 and CD276 with CAR T-cells demonstrates a strong antitumor impact against children rhabdomyosarcoma
CAR T-Cell therapy

Targeting FGFR4 and CD276 with CAR T-cells demonstrates a strong antitumor impact against children rhabdomyosarcoma

Chimeric antigen receptor (CAR) T-cells that specifically target Fibroblast Growth Factor Receptor 4 (FGFR4), a surface tyrosine receptor that is extensively expressed in rhabdomyosarcoma (RMS), are now undergoing clinical research. However, the effectiveness of these CAR T-cells may be hindered by tumor heterogeneity and inadequate activation. In this study, we present a method to enhance the co-stimulatory and targeting characteristics of a FGFR4 CAR through an optimization process. We substituted the hinge and transmembrane domain of CD8 as well as the 4-1BB co-stimulatory domain with the corresponding domains of CD28. The CARs produced exhibit heightened anti-tumor efficacy in multiple RMS xenograft models, with the exception of the RMS559 cell line, which is known for its aggressive nature.

Need help? Our team is ready to assist you.

We wish a speedy recovery of your dear and near one.

Start chat
We Are Online! Chat With Us!
Scan the code
Hello,

Welcome to CancerFax !

CancerFax is a pioneering platform dedicated to connecting individuals facing advanced-stage cancer with groundbreaking cell therapies like CAR T-Cell therapy, Gene therapy, TIL therapy, and clinical trials worldwide.

Let us know what we can do for you.

1) CAR T-Cell therapy
2) Gene therapy
3) Gamma-Delta T Cell therapy
4) TIL therapy
5) NK Cell therapy