儿童和青少年难治性/复发性霍奇金淋巴瘤患者的免疫检查点抑制剂疗法:一个病例系列

E. A. Tuzova, D. Evstratov, A. V. Pshonkin, M. N. Korsantiya, I. Fisyun, D. Litvinov, N. Myakova
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引用次数: 0

摘要

患有复发/难治性霍奇金淋巴瘤(r/r HL)的儿童、青少年和年轻成人的十年无进展生存率不超过 50%。Brentuximab vedotin(BV)和免疫检查点抑制剂(ICIs),如 nivolumab 和 pembrolizumab,已成功用于治疗成人复发性/难治性霍奇金淋巴瘤。在本研究中,我们分析了ICI治疗r/r HL儿童和青少年患者的经验。本研究为回顾性研究,纳入了接受 ICI 治疗的 18 岁以下 r/r HL 患者。共纳入 20 名患者。所有患者均接受过BV治疗,其中35%(n=7)的患者在接受ICIs治疗前接受过自体HSCT。在所有患者中,45%(9 人)因首次难治性复发而接受 ICIs 治疗,40%(8 人)因难治性疾病进展而接受 ICIs 治疗,15%(3 人)因第二次复发而接受 ICIs 治疗。两名患者接受了 ICIs 与其他药物的联合治疗,其中两名患者的治疗反应尚不明确。16名患者中有9名(56%)获得了代谢反应,1名患者根据正电子发射断层扫描阳性病灶的活检结果,没有证据表明存在重要的肿瘤细胞,因此有10名(63%)患者获得了反应。生存率分析包括 20 名患者。从开始使用 ICIs 起,中位随访时间为 1.2 年(四分位间范围:0.7-1.5 年)。1年总生存率(OS)达到69%(95%置信区间(CI)为46.4-91.6),2年OS为60.4%(95%置信区间(CI)为35.1-85.7),3年OS为40.3%(95%置信区间(CI)为4-76.6)。在这项研究中,我们证明了将 ICIs 作为治疗手段之一,对于那些对包括 BV 在内的既往治疗方案无效的 r/r HL 儿童和青少年患者的有效性。患者的父母同意将其子女的资料(包括照片)用于研究和出版。
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Immune checkpoint inhibitor therapy in children and adolescents with refractory/relapsed Hodgkin lymphoma: a case series
   Ten-year progression-free survival in children, adolescents and young adults with relapsed/refractory Hodgkin lymphoma (r/r HL) does not exceed 50 %. Brentuximab vedotin (BV) and immune checkpoint inhibitors (ICIs), such as nivolumab and pembrolizumab, are successfully used for the treatment of adults with r/r HL. In this study, we analyzed our experience of ICI treatment of children and adolescents with r/r HL. This study was retrospective and included patients with r/r HL under 18 years of age, who received ICI therapy. Twenty patients were included. All of them had been treated with BV, 35 % (n = 7) of patients had undergone auto-HSCT before treatment with ICIs. Among all patients, 45% (n = 9) received ICIs for the first refractory relapse, 40 % (n = 8) due to refractory disease progression and 15 % (n = 3) received therapy for the second relapse. Two patients received ICIs in combination with other drugs, the response to therapy in 2 patients was unknown. Nine (56 %) of 16 patients achieved a metabolic response, one patient had no evidence of vital tumor cells based on the results of a biopsy of a lesion positive on positron emission tomography, thus a response was achieved in 10 (63%) patients. The survival rate analysis included 20 patients. Median follow-up from ICIs initiation was 1.2 years (interquartile range: 0.7–1.5 years). The probability of 1-year overall survival (OS) rate reaches 69 % (95 % confidence interval (CI) 46.4–91.6), 2-year OS – 60.4 % (95 % CI 35.1–85.7), 3-year OS – 40.3 % (95 % CI 4–76.6). In this study, we demonstrated the effectiveness of the treatment with ICIs as an element of therapy in children and adolescents with r/r HL, who had not responded to previous lines of therapy, including BV. The patients' parents gave consent to the use of their children's data, including photographs, for research purposes and in publications.
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来源期刊
Pediatric Hematology/Oncology and Immunopathology
Pediatric Hematology/Oncology and Immunopathology Medicine-Pediatrics, Perinatology and Child Health
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0.40
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49
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