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ジャーナル・オブ・オンコロジーの研究と治療

オープンアクセス

当社グループは 3,000 以上の世界的なカンファレンスシリーズ 米国、ヨーロッパ、世界中で毎年イベントが開催されます。 1,000 のより科学的な学会からの支援を受けたアジア および 700 以上の オープン アクセスを発行ジャーナルには 50,000 人以上の著名人が掲載されており、科学者が編集委員として名高い

オープンアクセスジャーナルはより多くの読者と引用を獲得
700 ジャーナル 15,000,000 人の読者 各ジャーナルは 25,000 人以上の読者を獲得

抽象的な

Clinical Outcomes in Metastatic Melanoma Patients Treated with Pembrolizumab: A Single-Center Retrospective Cohort Study

Sarah Mansouri, Stéphanie Marcil, Jean-Philippe Dulude, Jonathan Noujaim Liu, Guy Leblanc, Mai Kim Gervais

Objectives: The aim of this study is to review the response rate and survival outcomes of patients with stage IV melanoma treated with pembrolizumab in our center.

Methods: Patients with pathologically confirmed metastatic melanoma referred to our center from 2015 to 2017 and treated with pembrolizumab were included in this study. Follow-up consisted of clinical evaluation and FDGPET scans every 3-months. The primary outcome was the response rate of pembrolizumab. Secondary outcomes included Overall Survival (OS), Progression-Free Survival (PFS), and adverse events of pembrolizumab. Long term outcomes of patients attaining complete response for which pembrolizumab was discontinued were also analyzed. Kaplan-Meier and log-rank tests were used to calculate OS and PFS.

Results: A total of 23 patients were included in the study; 7 patients had a BRAF mutation, 16 patients received The median number of pembrolizumab cycles to achieve a Complete Response (CR) was 11 cycles. Median OS and PFS were 60 months and 28 months, respectively, with a median follow-up of 27 months. At the time of data collection, 16 patients were alive and 11 of them disease free. Grade 3 and 4 adverse events occurred in less than 13% of the patients. There were no reported pembrolizumab adverse events leading to death.

Conclusion: Our results confirmed the previously reported high response rates and complete responses of pembrolizumab in patients with metastatic melanoma. Patients with CR in whom treatment was discontinued remained disease-free for the duration of our follow-up.