TY - JOUR
T1 - Immunotherapy in Hodgkin Lymphoma
T2 - The Road Ahead
AU - Ansell, Stephen M.
N1 - Funding Information:
S.M.A. receives research funding (to his institution) from Bristol Myers Squibb, Merck, Affimed, Celldex, Pfizer, Trillium, LAM Therapeutics, and Seattle Genetics.
Publisher Copyright:
© 2019 Elsevier Ltd
PY - 2019/5
Y1 - 2019/5
N2 - An extensive infiltrate of intratumoral immune cells is a hallmark of classic Hodgkin lymphoma (cHL) but these cells do result in an effective antitumor response. Immune checkpoint therapy, which activates ‘exhausted’ T cells, has been found to be highly effective in cHL, but responding patients commonly relapse. Combination approaches are currently being investigated but the assessment of benefit when adding immunotherapy is challenging. The pitfalls in designing combination studies derive from response endpoints that are difficult to measure, a lack of biomarkers that predict response, and a limited understanding of tumor biology. While progress in treating patients with cHL has been exceptional so far, further progress may require a review of clinical trial endpoints and a greater understanding of cHL biology.
AB - An extensive infiltrate of intratumoral immune cells is a hallmark of classic Hodgkin lymphoma (cHL) but these cells do result in an effective antitumor response. Immune checkpoint therapy, which activates ‘exhausted’ T cells, has been found to be highly effective in cHL, but responding patients commonly relapse. Combination approaches are currently being investigated but the assessment of benefit when adding immunotherapy is challenging. The pitfalls in designing combination studies derive from response endpoints that are difficult to measure, a lack of biomarkers that predict response, and a limited understanding of tumor biology. While progress in treating patients with cHL has been exceptional so far, further progress may require a review of clinical trial endpoints and a greater understanding of cHL biology.
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U2 - 10.1016/j.it.2019.03.003
DO - 10.1016/j.it.2019.03.003
M3 - Review article
C2 - 30948348
AN - SCOPUS:85063681387
SN - 1471-4906
VL - 40
SP - 380
EP - 386
JO - Trends in Immunology
JF - Trends in Immunology
IS - 5
ER -