Adjuvant immune checkpoint inhibitor therapy may benefit pediatric patients with stage III melanoma and sentinel lymph node positivity: a case series.

IF 1.2 4区 医学 Q4 HEMATOLOGY Pediatric Hematology and Oncology Pub Date : 2024-09-01 Epub Date: 2024-05-07 DOI:10.1080/08880018.2024.2350455
Acacia Bowden, Jeanette Zambito, Jinia El-Feghaly, Jeffrey R Andolina
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引用次数: 0

Abstract

Melanoma is the most common skin cancer in children. While the current literature establishes treatment protocols for adult-type melanoma, very few pediatric-specific studies exist, and children are often excluded from melanoma clinical trials2. We report a case series of 23 pediatric patients aged 2-20 years old diagnosed with melanoma at the University of Rochester Medical Center between 1/1/2011 and 1/1/2022. 9/23 patients were Stage III; all patients underwent wide local excision and 9 received adjuvant therapies. 2/23 (8.7%) patients had recurrence of their malignancy after therapy while 21/23 (91.3%) remained without disease progression; 1 patient died from unknown cause, but the rest are alive and currently without disease. All patients whose initial therapy included nivolumab in addition to wide local excision did not have recurrence or progression of their disease. This case series highlights trends in the presentation, treatment, and outcomes of pediatric melanoma; however, additional multi-center studies are needed to establish the clinical utility of such features in pediatric melanoma.

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辅助免疫检查点抑制剂疗法可使Ⅲ期黑色素瘤和前哨淋巴结阳性的儿科患者获益:一个病例系列。
黑色素瘤是儿童最常见的皮肤癌。目前的文献为成人型黑色素瘤制定了治疗方案,但针对儿童的研究却很少,而且儿童往往被排除在黑色素瘤临床试验之外2。我们报告了 2011 年 1 月 1 日至 2022 年 1 月 1 日期间在罗切斯特大学医学中心确诊为黑色素瘤的 23 名 2-20 岁儿童患者的系列病例。9/23例患者为III期;所有患者均接受了广泛局部切除术,9例接受了辅助治疗。2/23(8.7%)名患者在治疗后恶性肿瘤复发,21/23(91.3%)名患者的病情没有进展;1名患者死因不明,但其余患者均健在且目前没有患病。除了广泛局部切除术外,所有初始治疗包括 nivolumab 的患者都没有复发或病情进展。本系列病例强调了小儿黑色素瘤的表现、治疗和预后趋势;然而,要确定这些特征在小儿黑色素瘤中的临床实用性,还需要进行更多的多中心研究。
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来源期刊
CiteScore
2.60
自引率
5.90%
发文量
71
审稿时长
6-12 weeks
期刊介绍: PHO: Pediatric Hematology and Oncology covers all aspects of research and patient management within the area of blood disorders and malignant diseases of childhood. Our goal is to make PHO: Pediatric Hematology and Oncology the premier journal for the international community of clinicians and scientists who together aim to define optimal therapeutic strategies for children and young adults with cancer and blood disorders. The journal supports articles that address research in diverse clinical settings, exceptional case studies/series that add novel insights into pathogenesis and/or clinical care, and reviews highlighting discoveries and challenges emerging from consortia and conferences. Clinical studies as well as basic and translational research reports regarding cancer pathogenesis, genetics, molecular diagnostics, pharmacology, stem cells, molecular targeting, cellular and immune therapies and transplantation are of interest. Papers with a focus on supportive care, late effects and on related ethical, legal, psychological, social, cultural, or historical aspects of these fields are also appreciated. Reviews on important developments in the field are welcome. Articles from scientists and clinicians across the international community of Pediatric Hematology and Oncology are considered for publication. The journal is not dependent on or connected with any organization or society. All submissions undergo rigorous peer review prior to publication. Our Editorial Board includes experts in Pediatric Hematology and Oncology representing a wide range of academic and geographic diversity.
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