TY - JOUR
T1 - Retrospective study of advanced melanoma patients treated with ipilimumab after nivolumab
T2 - Analysis of 60 Japanese patients
AU - Fujisawa, Yasuhiro
AU - Yoshino, Koji
AU - Otsuka, Atsushi
AU - Funakoshi, Takeru
AU - Uchi, Hiroshi
AU - Fujimura, Taku
AU - Matsushita, Shigeto
AU - Hata, Hiroo
AU - Okuhira, Hisako
AU - Tanaka, Ryota
AU - Nagai, Kojiro
AU - Ishida, Yoshihiro
AU - Nakamura, Yoshio
AU - Furudate, Sadanori
AU - Yamamura, Kentaro
AU - Imafuku, Keisuke
AU - Yamamoto, Yuki
N1 - Funding Information:
We would like to thank Thomas Mayers of the Medical English Communication Center of the University of Tsukuba, for his excellent English revisions.
Publisher Copyright:
© 2017 Japanese Society for Investigative Dermatology
PY - 2018/1
Y1 - 2018/1
N2 - Background: Due to resistance and immune-related adverse events (irAE) some melanoma patients require ipilimumab after nivolumab therapy. However, little is known about the result of this switching. Objective: Investigate the outcome of ipilimumab switching in Japanese patients. Methods: We retrospectively collected 60 patients who were treated with ipilimumab after nivolumab from 9 institutes in Japan. Information of the primary tumor, treatment, response, irAE), and survival was collected. Results: In our cohort, acral lentiginous and mucosal melanoma accounted for 53% of the cases. The most common reason for initiating ipilimumab was disease progression (93%). Median interval from the last nivolumab administration to first ipilimumab administration was 29 days. Only 38% of patients completed 4 injections of ipilimumab. The best overall response was 3.6%. IrAE occurred in 78% of patients and 70% of those were of grade 3/4 (G3/4) and 31% of patients experienced 2 or more irAEs. An within interval of 28 days or less between the last nivolumab administration and ipilimumab administration was correlated with the development of G3/4 pyrexia and 3 or more irAEs, but irAE occurrence did not affect survival. Multivariate analysis showed that endocrine irAE (relative risk = 0.22, P = 0.015) and skin irAE (relative risk = 2.78, P = 0.048) were significant factors associated with survival. Conclusion: In our study, the response ratio to ipilimumab after nivolumab was unsatisfactory and associated with a high frequency of severe irAEs. As there are few second-line treatment options for patients with BRAF wild-type advanced melanoma after nivolumab failure, patients should be closely monitored if ipilimumab is initiated.
AB - Background: Due to resistance and immune-related adverse events (irAE) some melanoma patients require ipilimumab after nivolumab therapy. However, little is known about the result of this switching. Objective: Investigate the outcome of ipilimumab switching in Japanese patients. Methods: We retrospectively collected 60 patients who were treated with ipilimumab after nivolumab from 9 institutes in Japan. Information of the primary tumor, treatment, response, irAE), and survival was collected. Results: In our cohort, acral lentiginous and mucosal melanoma accounted for 53% of the cases. The most common reason for initiating ipilimumab was disease progression (93%). Median interval from the last nivolumab administration to first ipilimumab administration was 29 days. Only 38% of patients completed 4 injections of ipilimumab. The best overall response was 3.6%. IrAE occurred in 78% of patients and 70% of those were of grade 3/4 (G3/4) and 31% of patients experienced 2 or more irAEs. An within interval of 28 days or less between the last nivolumab administration and ipilimumab administration was correlated with the development of G3/4 pyrexia and 3 or more irAEs, but irAE occurrence did not affect survival. Multivariate analysis showed that endocrine irAE (relative risk = 0.22, P = 0.015) and skin irAE (relative risk = 2.78, P = 0.048) were significant factors associated with survival. Conclusion: In our study, the response ratio to ipilimumab after nivolumab was unsatisfactory and associated with a high frequency of severe irAEs. As there are few second-line treatment options for patients with BRAF wild-type advanced melanoma after nivolumab failure, patients should be closely monitored if ipilimumab is initiated.
KW - Checkpoint inhibitor
KW - Ipilimumab
KW - Melanoma
KW - Nivolumab
KW - Switching
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U2 - 10.1016/j.jdermsci.2017.10.009
DO - 10.1016/j.jdermsci.2017.10.009
M3 - Article
C2 - 29079332
AN - SCOPUS:85033453536
SN - 0923-1811
VL - 89
SP - 60
EP - 66
JO - Journal of Dermatological Science
JF - Journal of Dermatological Science
IS - 1
ER -