TY - JOUR
T1 - Pembrolizumab in the treatment of refractory primary mediastinal large B-cell lymphoma
T2 - safety and efficacy
AU - Camus, Vincent
AU - Bigenwald, Camille
AU - Ribrag, Vincent
AU - Lazarovici, Julien
AU - Jardin, Fabrice
AU - Sarkozy, Clémentine
N1 - Publisher Copyright:
© 2021 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2021/1/1
Y1 - 2021/1/1
N2 - Introduction: Primary mediastinal large B-cell lymphoma (PMBL) is a rare subtype of lymphoma, clinically and biologically distinct from diffuse large B-cell lymphoma (DLBCL) that shows overlapping features with classical Hodgkin lymphoma (cHL). If first-line strategies lead to 80–85% of curability, relapse occurs early with a chemo-refractory disease and a poor outcome. The presence of 9p24.1 rearrangement, conducting to the overexpression of the immune checkpoint molecules PDL1 and 2, has paved the way for immune checkpoint blockers development in these entities. Pembrolizumab, an anti PD-1 checkpoint antibody, was initially approved in solid cancer and later on in the lymphoma field in cHL. Areas covered: We summarize the biology and clinical need in PMBL, leading to the rationale for checkpoint inhibitors development, as well as pembrolizumab clinical studies in this entity. To do so, we performed a PubMed search using the terms: ‘PMBCL,’ ‘lymphoma,’ ‘Immune checkpoint,’ and ‘Pembrolizumab.’ Expert opinion: Pembrolizumab showed tolerable safety profile and efficacy data in patients with PMBL who have relapsed after, or are ineligible for autologous stem cell transplant (ASCT). Some combination strategies have shown promising preliminary results, while others are currently being conducted.
AB - Introduction: Primary mediastinal large B-cell lymphoma (PMBL) is a rare subtype of lymphoma, clinically and biologically distinct from diffuse large B-cell lymphoma (DLBCL) that shows overlapping features with classical Hodgkin lymphoma (cHL). If first-line strategies lead to 80–85% of curability, relapse occurs early with a chemo-refractory disease and a poor outcome. The presence of 9p24.1 rearrangement, conducting to the overexpression of the immune checkpoint molecules PDL1 and 2, has paved the way for immune checkpoint blockers development in these entities. Pembrolizumab, an anti PD-1 checkpoint antibody, was initially approved in solid cancer and later on in the lymphoma field in cHL. Areas covered: We summarize the biology and clinical need in PMBL, leading to the rationale for checkpoint inhibitors development, as well as pembrolizumab clinical studies in this entity. To do so, we performed a PubMed search using the terms: ‘PMBCL,’ ‘lymphoma,’ ‘Immune checkpoint,’ and ‘Pembrolizumab.’ Expert opinion: Pembrolizumab showed tolerable safety profile and efficacy data in patients with PMBL who have relapsed after, or are ineligible for autologous stem cell transplant (ASCT). Some combination strategies have shown promising preliminary results, while others are currently being conducted.
KW - Immune checkpoint
KW - Pembrolizumab
KW - Primary Mediastinal B Cell Lymphoma
UR - http://www.scopus.com/inward/record.url?scp=85113148889&partnerID=8YFLogxK
U2 - 10.1080/14737140.2021.1953986
DO - 10.1080/14737140.2021.1953986
M3 - Article
C2 - 34233557
AN - SCOPUS:85113148889
SN - 1473-7140
VL - 21
SP - 941
EP - 956
JO - Expert Review of Anticancer Therapy
JF - Expert Review of Anticancer Therapy
IS - 9
ER -