TY - JOUR
T1 - Investigation of clinical factors associated with longer overall survival in advanced melanoma patients treated with sequential ipilimumab
AU - Muto, Yusuke
AU - Kitano, Shigehisa
AU - Tsutsumida, Arata
AU - Namikawa, Kenjiro
AU - Takahashi, Akira
AU - Nakamura, Yoshio
AU - Yamanaka, Takeharu
AU - Yamamoto, Noboru
AU - Yamazaki, Naoya
N1 - Funding Information:
This work was supported in part by the National Cancer Center Research and Development Fund, JSPS KAKENHI (Grants-in-Aid for Scientific Research), and a Grant-in-Aid for Cancer Research from the Ministry of Health, Labor and Welfare of Japan.
Funding Information:
ACKNOWLEDGMENTS: This work was supported in part by the National Cancer Center Research and Development Fund, JSPS KAKENHI (Grants-in-Aid for Scientific Research), and a Grant-in-Aid for Cancer Research from the Ministry of Health, Labor and Welfare of Japan.
Funding Information:
member for Bristol-Myers Squibb, Ono, Novartis and MSD, and received research funds at the institutional level from Bristol-Myers Squibb, Ono, Novartis, MSD and Takara-Bio, as well as honoraria from Bristol-Myers Squibb, Ono, Novartis and MSD. T. Y. is a consultant/advisory board member for Gilead Sciences and Sysmex, and received honoraria from Chugai, Takeda, Taiho and Boehringer Ingelheim, as well as research funding from Takeda. K. N. has received honoraria from Ono Pharmaceutical, Bristol-Myers Squibb, MSD, Novartis Pharmaceutical, Toray industries, Eisai and Chugai Pharmaceutical. A. T. has received honoraria from Ono Pharmaceutical, Bristol-Myers Squibb and Novartis Pharmaceutical. The other authors have no potential conflicts of interest to disclose.
Publisher Copyright:
© 2019 Japanese Dermatological Association
PY - 2019/6
Y1 - 2019/6
N2 - Melanoma is one of the most serious form of skin cancer. Nowadays, ipilimumab is used for advanced melanoma refractory to first-line anti-programmed death 1 (PD-1) antibodies. Thirty patients (male : female ratio, 18:12; median age, 60.5 years) sequentially treated with ipilimumab after anti-PD-1 antibody (nivolumab or pembrolizumab), while 58 (male : female ratio, 27:31; median age, 66.5 years) with anti-PD-1 antibody only. The kind of therapy and schedules were as follows: nivolumab, 2 mg/kg at 3-week intervals or at 3 mg/kg every 2 week; pembrolizumab, 2 mg/kg every 3 weeks; ipilimumab, 3 mg/kg at 3-week intervals for four doses. The sequential therapy was selected for the patients with disease progression and/or recovered from severe (immune-related [ir]) adverse events (AE) after PD-1 blockade monotherapy. We evaluated multiple parameters and analyzed their relevance to overall survival (OS). The best objective response rate was 6.7% in sequential ipilimumab treatment. Median OS was 163 days (range, 16–489). Baseline absolute lymphocyte count (ALC) and performance status (PS) before sequential ipilimumab were associated with OS in univariate analyses. Baseline PS and irAE within 6 weeks after ipilimumab administration showed significant differences on multivariate analysis. Prior to first-line PD-1 blockade, these parameters were not associated with OS. The other factors (i.e. age, sex, number of doses, absolute neutrophil counts, neutrophil : lymphocyte ratio, lactate dehydrogenase and C-reactive protein) were not associated with OS. [Correction added on 17 April 2019, after first online publication: ‘not related to OS' has been amended to ‘not associated with OS’.] Ipilimumab as sequential therapy did not appear to improve OS and was associated with more severe irAE than PD-1 blockade monotherapy. We need to carefully consider treating patients with poor PS and low ALC.
AB - Melanoma is one of the most serious form of skin cancer. Nowadays, ipilimumab is used for advanced melanoma refractory to first-line anti-programmed death 1 (PD-1) antibodies. Thirty patients (male : female ratio, 18:12; median age, 60.5 years) sequentially treated with ipilimumab after anti-PD-1 antibody (nivolumab or pembrolizumab), while 58 (male : female ratio, 27:31; median age, 66.5 years) with anti-PD-1 antibody only. The kind of therapy and schedules were as follows: nivolumab, 2 mg/kg at 3-week intervals or at 3 mg/kg every 2 week; pembrolizumab, 2 mg/kg every 3 weeks; ipilimumab, 3 mg/kg at 3-week intervals for four doses. The sequential therapy was selected for the patients with disease progression and/or recovered from severe (immune-related [ir]) adverse events (AE) after PD-1 blockade monotherapy. We evaluated multiple parameters and analyzed their relevance to overall survival (OS). The best objective response rate was 6.7% in sequential ipilimumab treatment. Median OS was 163 days (range, 16–489). Baseline absolute lymphocyte count (ALC) and performance status (PS) before sequential ipilimumab were associated with OS in univariate analyses. Baseline PS and irAE within 6 weeks after ipilimumab administration showed significant differences on multivariate analysis. Prior to first-line PD-1 blockade, these parameters were not associated with OS. The other factors (i.e. age, sex, number of doses, absolute neutrophil counts, neutrophil : lymphocyte ratio, lactate dehydrogenase and C-reactive protein) were not associated with OS. [Correction added on 17 April 2019, after first online publication: ‘not related to OS' has been amended to ‘not associated with OS’.] Ipilimumab as sequential therapy did not appear to improve OS and was associated with more severe irAE than PD-1 blockade monotherapy. We need to carefully consider treating patients with poor PS and low ALC.
KW - absolute lymphocyte count
KW - anti-programmed death 1 antibody
KW - ipilimumab
KW - performance status
KW - sequential therapy
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U2 - 10.1111/1346-8138.14865
DO - 10.1111/1346-8138.14865
M3 - Article
C2 - 30945333
AN - SCOPUS:85063780154
SN - 0385-2407
VL - 46
SP - 498
EP - 506
JO - Journal of Dermatology
JF - Journal of Dermatology
IS - 6
ER -