医学
达布拉芬尼
曲美替尼
辅助治疗
黑色素瘤
内科学
肿瘤科
佐剂
转移性黑色素瘤
威罗菲尼
癌症研究
化疗
化学
生物化学
MAPK/ERK通路
激酶
作者
Ryo Amagai,Yusuke Muto,Hiroshi Katô,Satoru Matsushita,Takeo Maekawa,Satoshi Fukushima,Koji Yoshino,Hiroshi Uchi,Yasuhiro Fujisawa,Yuki Yamamoto,Kentaro Ohuchi,Yahiko Kambayashi,Taku Fujimura
出处
期刊:Melanoma Research
[Ovid Technologies (Wolters Kluwer)]
日期:2021-09-13
卷期号:31 (6): 575-578
被引量:5
标识
DOI:10.1097/cmr.0000000000000770
摘要
Patients with resected stage IIIB, IIIC and IIID melanomas have a high risk of recurrence. Therefore, an appropriate protocol for stage III melanoma is needed. Since adjuvant dabrafenib plus trametinib (D+T) combined therapy and anti-PD1 antibody (Ab) therapy reduce the risk of recurrence in patients with resected stage III BRAF-mutated melanoma, selecting the adjuvant therapy for BRAF-mutated melanoma is controversial. The efficacy and safety profiles of D+T combined therapy in the adjuvant setting were retrospectively analyzed in 36 Japanese. BRAF-mutated advanced melanoma patients. The relapse-free rate (RFR) at 12 months was 82.1% (95% confidential interval (CI), 63.9-92.6%). In the 21 patients who completed the protocol, the RFR at 12 months was 85.7% (95% CI, 64.5-95.9%). In the seven patients whose protocol was interrupted by adverse events, the RFR was 71.4% (95% CI, 35.2-92.4%). The incidence rate of any AEs for all patients was 69.7% (95% CI, 52.5-82.8%), including 13 cases of pyrexia, five cases of skin rash and four cases of liver dysfunction. The present study suggested that D+T therapy in the adjuvant setting is a useful and very tolerable protocol for BRAF-mutated melanoma in the Japanese population.
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