TY - JOUR
T1 - Management of relapsed/refractory classical Hodgkin lymphoma in transplant-ineligible patients
AU - Mehta-Shah, Neha
AU - Bartlett, Nancy L.
N1 - Funding Information:
Conflict-of-interest disclosure: N.L.B. has participated in advisory boards for Pfizer, KITE, and Seattle Genetics and has received institutional research funding from Affimed, Bristol-Myers Squibb, Celgene, Dynavax, Forty Seven, Genentech, Gilead, Idera, Immune Design, Incyte, Janssen, KITE, MedImmune, Merck & Co, Takeda, Novartis, Pfizer, Pharmacyclics. and Seattle Genetics. N.M.-S. has received research funding from Bristol-Myers Squibb, Celgene, and Verastem.
Publisher Copyright:
© 2018 by The American Society of Hematology.
PY - 2018/4/12
Y1 - 2018/4/12
N2 - Addition of brentuximab vedotin, a CD30-targeted antibody–drug conjugate, and the programmed death 1 (PD-1) inhibitors nivolumab and pembrolizumab to the arma-mentarium for transplant-ineligible relapsed/refractory classical Hodgkin lymphoma has resulted in improved outcomes, including the potential for cure in a small minority of patients. For patients who have failed prior transplant or are unsuitable for dose-intense approaches based on age or comorbidities, an individualized approach with sequential use of single agents such as brentuximab vedotin, PD-1 inhibitors, everolimus, lenalidomide, or conventional agents such as gemcitabine or vinorelbine may result in prolonged survival with a minimal or modest effect on quality of life. Participation in clinical trials evaluating new approaches such as combination immune checkpoint inhibition, novel antibody–drug conjugates, or cellular therapies such as Epstein-Barr virus–directed cytotoxic T lymphocytes and chimeric antigen receptor T cells offer additional options for eligible patients.
AB - Addition of brentuximab vedotin, a CD30-targeted antibody–drug conjugate, and the programmed death 1 (PD-1) inhibitors nivolumab and pembrolizumab to the arma-mentarium for transplant-ineligible relapsed/refractory classical Hodgkin lymphoma has resulted in improved outcomes, including the potential for cure in a small minority of patients. For patients who have failed prior transplant or are unsuitable for dose-intense approaches based on age or comorbidities, an individualized approach with sequential use of single agents such as brentuximab vedotin, PD-1 inhibitors, everolimus, lenalidomide, or conventional agents such as gemcitabine or vinorelbine may result in prolonged survival with a minimal or modest effect on quality of life. Participation in clinical trials evaluating new approaches such as combination immune checkpoint inhibition, novel antibody–drug conjugates, or cellular therapies such as Epstein-Barr virus–directed cytotoxic T lymphocytes and chimeric antigen receptor T cells offer additional options for eligible patients.
UR - http://www.scopus.com/inward/record.url?scp=85047873368&partnerID=8YFLogxK
U2 - 10.1182/blood-2017-09-772681
DO - 10.1182/blood-2017-09-772681
M3 - Article
C2 - 29500171
AN - SCOPUS:85047873368
SN - 0006-4971
VL - 131
SP - 1698
EP - 1703
JO - Blood
JF - Blood
IS - 15
ER -