2021
DOI: 10.3892/mco.2021.2287
|View full text |Cite
|
Sign up to set email alerts
|

Brentuximab vedotin maintenance after autologous stem cell transplantation for refractory gray zone lymphoma with long‑term remission

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
3
0

Year Published

2022
2022
2023
2023

Publication Types

Select...
3
1

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(3 citation statements)
references
References 13 publications
(19 reference statements)
0
3
0
Order By: Relevance
“…Recently, brentuximab vedotin, an anti-CD30 antibody, has been used to treat Hodgkin lymphoma and CD30-positive lymphoma[ 9 , 26 , 27 ]. Pembrolizumab, an anti-PD-L1 monoclonal antibody, is also used for patients with refractory GZL[ 28 ].…”
Section: Discussionmentioning
confidence: 99%
“…Recently, brentuximab vedotin, an anti-CD30 antibody, has been used to treat Hodgkin lymphoma and CD30-positive lymphoma[ 9 , 26 , 27 ]. Pembrolizumab, an anti-PD-L1 monoclonal antibody, is also used for patients with refractory GZL[ 28 ].…”
Section: Discussionmentioning
confidence: 99%
“…Based on the results observed in PMBL [27], a very recent publication has reported that the combination of brentuximab vedotin (BV), and nivolumab is effective in approximately 70% of patients with R/R MGZL [28]. BV is an anti-CD30 humanised monoclonal antibody conjugated with monomethyl auristatin E, and the expression of CD30 by tumour cells represents the rationale of its usage [28,29]. BV was found to be effective also as maintenance after ASCT in R/R MGZL [29].…”
Section: Therapeutic Strategiesmentioning
confidence: 99%
“…BV is an anti-CD30 humanised monoclonal antibody conjugated with monomethyl auristatin E, and the expression of CD30 by tumour cells represents the rationale of its usage [28,29]. BV was found to be effective also as maintenance after ASCT in R/R MGZL [29]. In addition to the target effect, BV may also induce an immunogenic environment contributing to the depletion of regulatory T-cells that can potentiate the effect of immune-checkpoint inhibitors, such as nivolumab [28].…”
Section: Therapeutic Strategiesmentioning
confidence: 99%