TY - JOUR
T1 - Real-world efficacy of anti-PD-1 antibody or combined anti-PD-1 plus anti-CTLA-4 antibodies, with or without radiotherapy, in advanced mucosal melanoma patients
T2 - A retrospective, multicenter study
AU - Umeda, Yoshiyasu
AU - Yoshikawa, Shusuke
AU - Kiniwa, Yukiko
AU - Maekawa, Takeo
AU - Yamasaki, Osamu
AU - Isei, Taiki
AU - Matsushita, Shigeto
AU - Nomura, Motoo
AU - Nakai, Yasuo
AU - Fukushima, Satoshi
AU - Saito, Shintaro
AU - Takenouchi, Tatsuya
AU - Tanaka, Ryo
AU - Kato, Hiroshi
AU - Otsuka, Atsushi
AU - Matsuya, Taisuke
AU - Baba, Natsuki
AU - Nagase, Kotaro
AU - Inozume, Takashi
AU - Onuma, Takehiro
AU - Kuwatsuka, Yutaka
AU - Fujimoto, Noriki
AU - Kaneko, Takahide
AU - Onishi, Masazumi
AU - Namikawa, Kenjiro
AU - Yamazaki, Naoya
AU - Nakamura, Yasuhiro
N1 - Funding Information:
Yoshiyasu Umeda has received honoraria from Ono and Novartis Pharma. Shusuke Yoshikawa has received honoraria from Novartis and Ono Pharma. Yukiko Kiniwa has received honoraria from Novartis and Ono Pharma. Takeo Maekawa has received honoraria from Bristol-Myers Squibb (BMS), Merck Sharp & Dohme (MSD), Novartis, and Ono Pharma. Osamu Yamasaki has received research funding or/and honoraria from Ono Pharma. Taiki Isei has served as a consultant or/and has received honoraria from Ono, Pfizer, BMS, and Novartis Pharma. Shigeto Matsushita has received honoraria from Ono Pharma. Motoo Nomura has no conflicts of interest to disclose. Yasuo Nakai has no conflicts of interest to disclose. Satoshi Fukushima has received research funding from Ono Pharma. Shintaro Saito has received honoraria from Ono Pharma. Tatsuya Takenouchi has no conflicts of interest to disclose. Ryo Tanaka has no conflicts of interest to disclose. Hiroshi Kato has received honoraria from Novartis and Ono Pharma. Atsushi Otsuka has served as a consultant or/and has received honoraria from BMS, MSD, Novartis, Ono and received research funding from Eisai. Taisuke Matsuya has no conflicts of interest to disclose. Natsuki Baba has no conflicts of interest to disclose. Kotaro Nagase has no conflicts of interest to disclose. Takashi Inozume has received honoraria from BMS, MSD, and Ono Pharma. Takehiro Onuma has no conflicts of interest to disclose. Yutaka Kuwatsuka has no conflicts of interest to disclose. Noriki Fujimoto has no conflicts of interest to disclose. Takahide Kaneko has no conflicts of interest to disclose. Masazumi Onishi has no conflicts of interest to disclose. Kenjiro Namikawa has served as a consultant or/and has received honoraria from BMS, Eisai, MSD, Novartis, Ono, Pharma International, Toray Industries, and Takara Bio Pharma. Naoya Yamazaki receives institutional research funding from Bristol-Myers Squibb, MSD, Novartis, Ono, and Takara Bio, and has served as consultant or/and has received honoraria from BMS, MSD, Novartis, and Ono Pharma. Yasuhiro Nakamura has served as a consultant or/and has received honoraria from MSD, Novartis, BMS, Maruho, Ono, Taisho Toyama, and Taiho Pharma.
Funding Information:
Yoshiyasu Umeda has received honoraria from Ono and Novartis Pharma. Shusuke Yoshikawa has received honoraria from Novartis and Ono Pharma. Yukiko Kiniwa has received honoraria from Novartis and Ono Pharma. Takeo Maekawa has received honoraria from Bristol-Myers Squibb (BMS), Merck Sharp & Dohme (MSD), Novartis, and Ono Pharma. Osamu Yamasaki has received research funding or/and honoraria from Ono Pharma . Taiki Isei has served as a consultant or/and has received honoraria from Ono, Pfizer, BMS, and Novartis Pharma. Shigeto Matsushita has received honoraria from Ono Pharma. Motoo Nomura has no conflicts of interest to disclose. Yasuo Nakai has no conflicts of interest to disclose. Satoshi Fukushima has received research funding from Ono Pharma . Shintaro Saito has received honoraria from Ono Pharma. Tatsuya Takenouchi has no conflicts of interest to disclose. Ryo Tanaka has no conflicts of interest to disclose. Hiroshi Kato has received honoraria from Novartis and Ono Pharma. Atsushi Otsuka has served as a consultant or/and has received honoraria from BMS, MSD, Novartis, Ono and received research funding from Eisai . Taisuke Matsuya has no conflicts of interest to disclose. Natsuki Baba has no conflicts of interest to disclose. Kotaro Nagase has no conflicts of interest to disclose. Takashi Inozume has received honoraria from BMS, MSD, and Ono Pharma. Takehiro Onuma has no conflicts of interest to disclose. Yutaka Kuwatsuka has no conflicts of interest to disclose. Noriki Fujimoto has no conflicts of interest to disclose. Takahide Kaneko has no conflicts of interest to disclose. Masazumi Onishi has no conflicts of interest to disclose. Kenjiro Namikawa has served as a consultant or/and has received honoraria from BMS, Eisai, MSD, Novartis, Ono, Pharma International, Toray Industries, and Takara Bio Pharma. Naoya Yamazaki receives institutional research funding from Bristol-Myers Squibb , MSD , Novartis , Ono, and Takara Bio , and has served as consultant or/and has received honoraria from BMS, MSD, Novartis, and Ono Pharma. Yasuhiro Nakamura has served as a consultant or/and has received honoraria from MSD, Novartis, BMS, Maruho, Ono, Taisho Toyama, and Taiho Pharma.
Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2021/11
Y1 - 2021/11
N2 - Background: Immune checkpoint inhibitors (ICIs) have a lower efficacy in mucosal melanoma (MUM) than in cutaneous melanoma. The use of combination treatments with radiotherapy (RT) to improve the efficacy in MUM, however, requires further investigation. Methods: We retrospectively evaluated 225 advanced MUM patients treated with anti-PD-1 monotherapy (PD1; 115) or anti-PD-1 + anti-CTLA-4 combination therapy (PD1+CTLA4; 42) with or without RT (56 and 12, respectively). Treatment efficacy was estimated by determining the objective response rate (ORR) and survival rate with the Kaplan–Meier analysis. Results: The baseline characteristics between the two groups in each ICI cohort were similar, except for Eastern Cooperative Oncology Group performance status in the PD1 cohort. No significant differences in ORR, progression-free survival (PFS), and overall survival (OS) were observed between the PD1 alone and PD1+RT groups in the PD1 cohort (ORR 26% versus 27%, P > 0.99; median PFS 6.2 versus 6.8 months, P = 0.63; median OS 19.2 versus 23.1 months, P = 0.70) or between the PD1+CTLA alone and PD1+CTLA4+RT groups in the PD1+CTLA4 cohort (ORR 28% vs 25%, P = 0.62; median PFS 5.8 versus 3.5 months, P = 0.21; median OS 31.7 versus 19.8 months, P = 0.79). Cox multivariate analysis indicated that RT in addition to PD1 or PD1+CTLA4 did not have a positive impact on the PFS or OS. Conclusions: A prolonged survival benefit with RT in combination with ICIs was not identified for advanced MUM patients, although RT may improve local control of the tumour and relieve local symptoms.
AB - Background: Immune checkpoint inhibitors (ICIs) have a lower efficacy in mucosal melanoma (MUM) than in cutaneous melanoma. The use of combination treatments with radiotherapy (RT) to improve the efficacy in MUM, however, requires further investigation. Methods: We retrospectively evaluated 225 advanced MUM patients treated with anti-PD-1 monotherapy (PD1; 115) or anti-PD-1 + anti-CTLA-4 combination therapy (PD1+CTLA4; 42) with or without RT (56 and 12, respectively). Treatment efficacy was estimated by determining the objective response rate (ORR) and survival rate with the Kaplan–Meier analysis. Results: The baseline characteristics between the two groups in each ICI cohort were similar, except for Eastern Cooperative Oncology Group performance status in the PD1 cohort. No significant differences in ORR, progression-free survival (PFS), and overall survival (OS) were observed between the PD1 alone and PD1+RT groups in the PD1 cohort (ORR 26% versus 27%, P > 0.99; median PFS 6.2 versus 6.8 months, P = 0.63; median OS 19.2 versus 23.1 months, P = 0.70) or between the PD1+CTLA alone and PD1+CTLA4+RT groups in the PD1+CTLA4 cohort (ORR 28% vs 25%, P = 0.62; median PFS 5.8 versus 3.5 months, P = 0.21; median OS 31.7 versus 19.8 months, P = 0.79). Cox multivariate analysis indicated that RT in addition to PD1 or PD1+CTLA4 did not have a positive impact on the PFS or OS. Conclusions: A prolonged survival benefit with RT in combination with ICIs was not identified for advanced MUM patients, although RT may improve local control of the tumour and relieve local symptoms.
KW - Abscopal effect
KW - Anti-CTLA-4 antibody
KW - Anti-PD-1 antibody
KW - Ipilimumab
KW - Mucosal melanoma
KW - Nivolumab
KW - Pembrolizumab
KW - Radiotherapy
UR - http://www.scopus.com/inward/record.url?scp=85115410908&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85115410908&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2021.08.034
DO - 10.1016/j.ejca.2021.08.034
M3 - Article
C2 - 34563991
AN - SCOPUS:85115410908
SN - 0959-8049
VL - 157
SP - 361
EP - 372
JO - European Journal of Cancer
JF - European Journal of Cancer
ER -