Efficacy comparison between anti-PD-1 antibody monotherapy and anti-PD-1 plus anti-CTLA-4 combination therapy as first-line immunotherapy for advanced acral melanoma: A retrospective, multicenter study of 254 Japanese patients

被引:24
|
作者
Nakamura, Yasuhiro [1 ,27 ]
Namikawa, Kenjiro [2 ]
Kiniwa, Yukiko [3 ]
Kato, Hiroshi [4 ]
Yamasaki, Osamu [5 ]
Yoshikawa, Shusuke [6 ]
Maekawa, Takeo [7 ]
Matsushita, Shigeto [8 ]
Takenouchi, Tatsuya [9 ]
Inozume, Takashi [10 ]
Nakai, Yasuo [11 ]
Fukushima, Satoshi [12 ]
Saito, Shintaro [13 ]
Otsuka, Atsushi [14 ,15 ]
Fujimoto, Noriki [16 ]
Isei, Taiki [17 ]
Baba, Natsuki [18 ]
Matsuya, Taisuke [19 ]
Tanaka, Ryo [20 ]
Kaneko, Takahide [21 ]
Onishi, Masazumi [22 ]
Kuwatsuka, Yutaka [23 ]
Nagase, Kotaro [24 ]
Onuma, Takehiro [25 ]
Nomura, Motoo [26 ]
Umeda, Yoshiyasu [1 ,20 ]
Yamazaki, Naoya [2 ]
机构
[1] Saitama Med Univ, Dept Skin Oncol Dermatol, Int Med Ctr, Saitama, Japan
[2] Natl Canc Ctr, Dept Dermatol Oncol, Tokyo, Japan
[3] Shinshu Univ, Dept Dermatol, Matsumoto, Japan
[4] Nagoya City Univ, Dept Geriatr & Environm Dermatol, Grad Sch Med Sci, Nagoya, Japan
[5] Okayama Univ, Dept Dermatol, Dent & Pharmaceut Sci, Grad Sch Med, Okayama, Japan
[6] Shizuoka Canc Ctr, Dermatol Div, Shizuoka, Japan
[7] Jichi Med Univ, Dept Dermatol, Tochigi, Japan
[8] Natl Hosp Org, Dept Dermato Oncol Dermatol, Kagoshima Med Ctr, Kagoshima, Japan
[9] Niigata Canc Ctr Hosp, Dept Dermatol, Niigata, Japan
[10] Chiba Univ, Dept Dermatol, Chiba, Japan
[11] Mie Univ, Dept Dermatol, Mie, Japan
[12] Kumamoto Univ, Fac Life Sci, Dept Dermatol & Plast Surg, Kumamoto, Japan
[13] Gunma Univ, Dept Dermatol, Grad Sch Med, Maebashi, Japan
[14] Kyoto Univ, Dept Dermatol, Kyoto, Japan
[15] Kindai Univ Hosp, Dept Dermatol, Osaka, Japan
[16] Shiga Univ Med Sci, Dept Dermatol, Otsu, Japan
[17] Osaka Int Canc Inst, Dept Dermatol Oncol, Osaka, Japan
[18] Univ Fukui, Dept Dermatol, Fukui, Japan
[19] Asahikawa Med Univ, Dept Dermatol, Asahikawa, Japan
[20] Kawasaki Med Sch, Dept Dermatol, Kurashiki, Japan
[21] Juntendo Univ, Dept Dermatol, Urayasu Hosp, Chiba, Japan
[22] Iwate Med Univ, Dept Dermatol, Iwate, Japan
[23] Nagasaki Univ, Dept Dermatol, Nagasaki, Japan
[24] Saga Univ, Fac Med, Dept Internal Med, Div Dermatol, Saga, Japan
[25] Univ Yamanashi, Dept Dermatol, Yamanashi, Japan
[26] Kyoto Univ, Dept Clin Oncol, Kyoto, Japan
[27] Saitama Med Univ, Dept Skin Oncol Dermatol, Int Med Ctr, 1397-1 Yamane, Saitama 3501298, Japan
关键词
CTLA-4; antigen; Immunotherapy; Ipilimumab; Melanoma; Nivolumab; Pembrolizumab; Programmed cell death 1 receptor; Retrospective studies; Japan; SINGLE-ARM; OPEN-LABEL; PD-1; BLOCKADE; PHASE-II; MUCOSAL; IPILIMUMAB; INHIBITORS; NIVOLUMAB; MUTATION; SAFETY;
D O I
10.1016/j.ejca.2022.08.030
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Although anti-PD-1 antibody monotherapy (PD-1) is commonly used to treat advanced acral melanoma (AM), its efficacy is limited. Further, data on the efficacy of PD-1 plus anti-CTLA-4 antibody (PD-1+CTLA-4) for the treatment of AM are limited. Therefore, we compared the efficacy of PD-1+CTLA-4 and PD-1 in the treatment of Japanese patients with advanced AM. Methods: This retrospective study evaluated patients with advanced AM who were treated with PD-1 or PD-1+CTLA-4 as first-line immunotherapy in 24 Japanese institutions between 2014 and 2020. Treatment efficacy focussing on the objective response rate (ORR), progression-free survival (PFS), and overall survival (OS) was compared between the two groups. Results: In total, 254 patients (palm and sole melanoma [PSM], n = 180; nail apparatus melanoma [NAM], n = 74) were included. Among the patients with PSM, the ORR (19% vs. 31%; P = 0.44), PFS (5.9 vs. 3.2 months; P = 0.74), and OS (23.1 vs. not reached; P = 0.55) did not differ significantly between the PD-1 and PD-1+CTLA-4 groups. Among the patients with NAM, the ORR (61% vs. 10%; P < 0.001) was significantly higher and PFS was longer (6.4 vs. 3.8 months; P = 0.10) in the PD-1+CTLA-4 group than in the PD-1 group. Cox multivariate analysis demonstrated that PD-1+CTLA-4 is an independent predictor of a favourable PFS in patients with NAM (P = 0.002). Conclusions: The efficacy of PD-1+CTLA-4 is not superior to that of PD-1 for the treatment of advanced PSM. However, PD-1+CTLA-4 may be more efficacious than PD-1 for the treatment of advanced NAM. (C) 2022 Elsevier Ltd. All rights reserved.
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收藏
页码:78 / 87
页数:10
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