Outcomes of adjuvant immune checkpoint inhibitor therapy in melanoma: a retrospective study.

IF 1.6 4区 医学 Q2 Medicine Acta Clinica Belgica Pub Date : 2024-09-13 DOI:10.1080/17843286.2024.2402622
Fieuws Sarah,De Ridder Margot,Baert Valerie,Decruyenaere Alexander,Brochez Lieve,Rottey Sylvie,Jacobs Celine,Saerens Michael
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Abstract

BACKGROUND Adjuvant treatment of malignant melanoma has improved the outcomes for patients. However, real-world data on efficacy and safety are limited. We investigated outcomes of melanoma patients treated with adjuvant immune checkpoint inhibitors (ICI) in the Ghent University Hospital. METHODS Patients with melanoma (stage III-IV), who received at least one cycle of ICI as adjuvant treatment between 2018 and 2021 were included in this retrospective cohort study. Primary outcomes were recurrence-free (RFS) and overall survival (OS). Other outcomes of interest were relapse patterns and safety. RESULTS 59 patients were included, with a median follow-up of 36 months. Disease recurrence or death of any cause was observed in 25/59 (42.4%) of the patients. The median RFS was 56.0 months (95%CI 36.1-75.9 months). At 48 months, RFS and OS were 55.9% and 84%, respectively. 9/23 (39%) recurrences were locoregional and 14/23 (60.9%) patients developed distant metastasis as first recurrence, including 2 (3.4%) with brain metastasis. Median time to recurrence was 9 months (range 2-56 months). 35/59 (59.3%) completed one year of adjuvant treatment, 12/59 (20.3%) stopped because of recurrence and 10/59 (16.9% because of toxicity. Immune-related adverse events wereseen in 29/59 (49.4%) patients, 10/59 (16.9%) developed grade 3-4 toxicity. CONCLUSION This study confirms the real-world efficacy and safety of adjuvant ICI for melanoma, achieving RFS and OS comparableto the pivotal clinical trials. About 40% of patients develop arelapse, mainly during the adjuvant treatment. The outcomes ofpatients progressing during adjuvant ICI are poor, emphasizing the need of prospective and real-world studies on optimal management after progression on (neo)adjuvant treatment.
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黑色素瘤辅助免疫检查点抑制剂疗法的疗效:一项回顾性研究。
背景恶性黑色素瘤的辅助治疗改善了患者的预后。然而,有关疗效和安全性的实际数据却很有限。我们调查了根特大学医院接受免疫检查点抑制剂(ICI)辅助治疗的黑色素瘤患者的预后情况。方法这项回顾性队列研究纳入了2018年至2021年间接受至少一个周期ICI辅助治疗的黑色素瘤患者(III-IV期)。主要结果为无复发(RFS)和总生存率(OS)。其他相关结果为复发模式和安全性。结果共纳入59例患者,中位随访时间为36个月。25/59(42.4%)名患者因任何原因导致疾病复发或死亡。中位 RFS 为 56.0 个月(95%CI 36.1-75.9 个月)。48 个月时,RFS 和 OS 分别为 55.9% 和 84%。9/23(39%)例复发为局部复发,14/23(60.9%)例患者首次复发为远处转移,其中2例(3.4%)为脑转移。中位复发时间为9个月(2-56个月)。35/59(59.3%)名患者完成了一年的辅助治疗,12/59(20.3%)名患者因复发而停止治疗,10/59(16.9%)名患者因毒性而停止治疗。29/59(49.4%)名患者出现了免疫相关不良事件,10/59(16.9%)名患者出现了 3-4 级毒性。结论这项研究证实了 ICI 辅助治疗黑色素瘤的实际疗效和安全性,其 RFS 和 OS 达到了关键临床试验的水平。约40%的患者会出现病情进展,主要是在辅助治疗期间。在 ICI 辅助治疗期间病情进展的患者疗效不佳,因此需要对(新)辅助治疗进展后的最佳治疗方法进行前瞻性和真实世界研究。
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来源期刊
Acta Clinica Belgica
Acta Clinica Belgica 医学-医学:内科
CiteScore
2.90
自引率
0.00%
发文量
44
审稿时长
6-12 weeks
期刊介绍: Acta Clinica Belgica: International Journal of Clinical and Laboratory Medicine primarily publishes papers on clinical medicine, clinical chemistry, pathology and molecular biology, provided they describe results which contribute to our understanding of clinical problems or describe new methods applicable to clinical investigation. Readership includes physicians, pathologists, pharmacists and physicians working in non-academic and academic hospitals, practicing internal medicine and its subspecialties.
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