TY - JOUR
T1 - Nivolumab for the treatment of unresectable pleural mesothelioma
AU - Hotta, Katsuyuki
AU - Fujimoto, Nobukazu
AU - Kozuki, Toshiyuki
AU - Aoe, Keisuke
AU - Kiura, Katsuyuki
N1 - Funding Information:
One of the reviewers on this manuscript has received consulting fees from Epizyme, Aldeyra, Novocure, and Atara; speaking honorarium from Medical Learning Institute; research funding to MSK: MedImmune, Epizyme, Polaris, Sellas Life Sciences, Bristol-Myers Squibb, Millenium, Roche, and Curis; and holds a leadership position in the Mesothelioma Applied Research Foundation (uncompensated). Peer reviewers on this manuscript have no other relevant financial relationships or otherwise to disclose.
Funding Information:
This study was supported by grants-in-aid from the Ministry of Health, Labor, and Welfare, Japan.
Publisher Copyright:
© 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2020/2/1
Y1 - 2020/2/1
N2 - Introduction: Platinum-based chemotherapy is the current first-line standard therapy for unresectable malignant pleural mesothelioma (MPM). Recently, immune-checkpoint inhibitors (ICI) have been intensively investigated as treatment options for this disease. Nivolumab, an anti-programmed cell death (PD)-1 agent, was one of the first drugs used and is representative of available ICIs. Areas covered: This review discusses previous relevant reports and current ongoing trials of nivolumab. The efficacy and safety of nivolumab have been investigated mostly in second-line or later treatment settings as both monotherapy and in combination with other ICIs. Particularly, nivolumab monotherapy yielded promising efficacy with an objective response rate of 29% and median overall survival of 17.3 months in salvage settings in the single-arm, Japanese phase 2 trial (MERIT). Notably, the study led to Japanese approval of nivolumab for unresectable recurrent MPM. Several trials with monotherapy or cotherapy with nivolumab have commenced, including randomized trials of nivolumab monotherapy vs. placebo in the salvage setting, and cotherapy with nivolumab and ipilimumab vs. the platinum doublet in the frontline setting. Expert opinion: Nivolumab seems like a reasonable option for unresectable, relapsed MPM despite the lack of randomized trial data. Ongoing pivotal trials will confirm its efficacy.
AB - Introduction: Platinum-based chemotherapy is the current first-line standard therapy for unresectable malignant pleural mesothelioma (MPM). Recently, immune-checkpoint inhibitors (ICI) have been intensively investigated as treatment options for this disease. Nivolumab, an anti-programmed cell death (PD)-1 agent, was one of the first drugs used and is representative of available ICIs. Areas covered: This review discusses previous relevant reports and current ongoing trials of nivolumab. The efficacy and safety of nivolumab have been investigated mostly in second-line or later treatment settings as both monotherapy and in combination with other ICIs. Particularly, nivolumab monotherapy yielded promising efficacy with an objective response rate of 29% and median overall survival of 17.3 months in salvage settings in the single-arm, Japanese phase 2 trial (MERIT). Notably, the study led to Japanese approval of nivolumab for unresectable recurrent MPM. Several trials with monotherapy or cotherapy with nivolumab have commenced, including randomized trials of nivolumab monotherapy vs. placebo in the salvage setting, and cotherapy with nivolumab and ipilimumab vs. the platinum doublet in the frontline setting. Expert opinion: Nivolumab seems like a reasonable option for unresectable, relapsed MPM despite the lack of randomized trial data. Ongoing pivotal trials will confirm its efficacy.
KW - CTLA-4
KW - Mesothelioma
KW - PD-1
KW - PD-L1
KW - immune checkpoint inhibitor
UR - http://www.scopus.com/inward/record.url?scp=85076821749&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85076821749&partnerID=8YFLogxK
U2 - 10.1080/14712598.2020.1703945
DO - 10.1080/14712598.2020.1703945
M3 - Article
C2 - 31825692
AN - SCOPUS:85076821749
SN - 1471-2598
VL - 20
SP - 109
EP - 114
JO - Expert Opinion on Biological Therapy
JF - Expert Opinion on Biological Therapy
IS - 2
ER -