Upfront Management of Blastoid Variant Mantle Cell Lymphoma: Making the Case for 2nd/3rd‐Generation Bruton Tyrosine Kinase Inhibitor‐Based Therapies

Fuente: Wiley Open Access
Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Benjamin J. Lee, Jenny Liu, Shawn P. Griffin, Jean Doh, Stefan O. Ciurea, Piyanuch Kongtim, Elizabeth A. Brem
Format: Artículo Open Access
Veröffentlicht: Wiley 2024
Schlagworte:
Online-Zugang:
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
_version_ 1867015504118415360
author Benjamin J. Lee
Jenny Liu
Shawn P. Griffin
Jean Doh
Stefan O. Ciurea
Piyanuch Kongtim
Elizabeth A. Brem
author_facet Benjamin J. Lee
Jenny Liu
Shawn P. Griffin
Jean Doh
Stefan O. Ciurea
Piyanuch Kongtim
Elizabeth A. Brem
Benjamin J. Lee
Jenny Liu
Shawn P. Griffin
Jean Doh
Stefan O. Ciurea
Piyanuch Kongtim
Elizabeth A. Brem
collection Wiley Open Access
contents Upfront Management of Blastoid Variant Mantle Cell Lymphoma: Making the Case for 2nd/3rd‐Generation Bruton Tyrosine Kinase Inhibitor‐Based Therapies Benjamin J. Lee Jenny Liu Shawn P. Griffin Jean Doh Stefan O. Ciurea Piyanuch Kongtim Elizabeth A. Brem Cancer Medicine ABSTRACTIntroductionBlastoid variant‐mantle cell lymphoma (BV‐MCL) represents an aggressive subset of patients with no established standard of care treatment approach.MethodsWe performed a retrospective analysis of the clinical characteristics and outcomes of 17 de novo BV‐MCL patients treated at our institution between May 2009 and September 2023. In addition, we reviewed the literature supporting 2nd/3rd generation Bruton's Tyrosine‐kinase (BTKi)‐based therapies for upfront management.ResultsThe complete response rate to frontline and salvage therapy was 66.7% and 25%, respectively. Two‐year overall survival (OS) was low at 62.5% (95% CI, 34.7%–81.1%). Variables associated with higher OS included receipt of consolidative HSCT (p = 0.017), TP53‐wild type (p = 0.031), intermediate‐ versus high‐risk Mantle Cell Lymphoma Prognostic Index score (p = 0.026), and achieving complete response with induction therapy (p = 0.027).DiscussionTreatment outcomes with chemo‐immunotherapy in BV‐MCL patients are poor, especially among TP53‐mutated patients. Recent findings describing positive outcomes with novel BTKi‐based therapies are encouraging and should be considered in this high‐risk population. 10.1002/cam4.70310 http://creativecommons.org/licenses/by/4.0/
doi_str_mv 10.1002/cam4.70310
format Artículo Open Access
id wiley_oa_10_1002_cam4_70310
institution Wiley Open Access
license_str_mv http://creativecommons.org/licenses/by/4.0/
publishDate 2024
publisher Wiley
record_format wiley_oa
spellingShingle Upfront Management of Blastoid Variant Mantle Cell Lymphoma: Making the Case for 2nd/3rd‐Generation Bruton Tyrosine Kinase Inhibitor‐Based Therapies
Benjamin J. Lee
Jenny Liu
Shawn P. Griffin
Jean Doh
Stefan O. Ciurea
Piyanuch Kongtim
Elizabeth A. Brem
Cancer Medicine
Upfront Management of Blastoid Variant Mantle Cell Lymphoma: Making the Case for 2nd/3rd‐Generation Bruton Tyrosine Kinase Inhibitor‐Based Therapies Benjamin J. Lee Jenny Liu Shawn P. Griffin Jean Doh Stefan O. Ciurea Piyanuch Kongtim Elizabeth A. Brem Cancer Medicine ABSTRACTIntroductionBlastoid variant‐mantle cell lymphoma (BV‐MCL) represents an aggressive subset of patients with no established standard of care treatment approach.MethodsWe performed a retrospective analysis of the clinical characteristics and outcomes of 17 de novo BV‐MCL patients treated at our institution between May 2009 and September 2023. In addition, we reviewed the literature supporting 2nd/3rd generation Bruton's Tyrosine‐kinase (BTKi)‐based therapies for upfront management.ResultsThe complete response rate to frontline and salvage therapy was 66.7% and 25%, respectively. Two‐year overall survival (OS) was low at 62.5% (95% CI, 34.7%–81.1%). Variables associated with higher OS included receipt of consolidative HSCT (p = 0.017), TP53‐wild type (p = 0.031), intermediate‐ versus high‐risk Mantle Cell Lymphoma Prognostic Index score (p = 0.026), and achieving complete response with induction therapy (p = 0.027).DiscussionTreatment outcomes with chemo‐immunotherapy in BV‐MCL patients are poor, especially among TP53‐mutated patients. Recent findings describing positive outcomes with novel BTKi‐based therapies are encouraging and should be considered in this high‐risk population. 10.1002/cam4.70310 http://creativecommons.org/licenses/by/4.0/
title Upfront Management of Blastoid Variant Mantle Cell Lymphoma: Making the Case for 2nd/3rd‐Generation Bruton Tyrosine Kinase Inhibitor‐Based Therapies
topic Cancer Medicine
url https://onlinelibrary.wiley.com/doi/10.1002/cam4.70310