Kokkali Stefania, Kotsantis Ioannis, Magou Elpida, Sophia Talagani, Kormas Theodoros, Diakoumis Giakoumis, Spathas Nikolaos, Psyrri Amanda, Ardavanis Alexandros
First Medical Oncology Clinic, Saint-Savvas Cancer Hospital, Athens, Greece.
Section of Medical Oncology, 2nd Department of Medicine and Laboratory, Faculty of Medicine, National and Kapodistrian University of Athens, Hippocratio General Hospital of Athens, Athens, Greece.
Invest New Drugs. 2022 Jun;40(3):668-675. doi: 10.1007/s10637-022-01225-7. Epub 2022 Mar 21.
Current treatment recommendations for high grade non-metastatic osteosarcoma include perioperative chemotherapy and surgery. Despite this intensive protocol, approximately 40% of patients will relapse. The addition of the immunomodulator mifamurtide to adjuvant cytotoxic chemotherapy was associated with a significant improvement in 6-year overall survival (OS) in young patients with resectable osteosarcoma, leading to its approval in Europe and other countries. Very limited real-world data are reported on its use.
We retrospectively evaluated data from osteosarcoma patients who received mifamurtide in the adjuvant setting. Data were obtained from medical records in 2 high-volume bone sarcoma centers. The aim of this study was to collect real-world data on mifamurtide safety and efficacy in Greece.
We identified 15 patients with completely resected osteosarcoma who received mifamurtide from September 2015 to January 2020. Median age at diagnosis was 24 years old (16-76). Osteosarcoma arose in the lower extremities (n = 12), in the upper extremities (n = 2) or in the ilium (n = 1). The majority of patients (n = 13) received cisplatin/doxorubicin/methotrexate as perioperative chemotherapy and the remaining patients cisplatin/doxorubicin. After a median follow-up of 46.9 months (range, 32.8-61.1), the median recurrence-free survival was 58.7 months (range, 18.5-98.8) and the median OS 64.1 months (range, 25.6-102.6). Except for fever and chills, the only adverse event probably related to mifamurtide was pericarditis (n = 1).
Mifamurtide was well tolerated in a Greek osteosarcoma population, including patients older than 30 years. The small sample size and the non-comparative design do not allow drawing conclusions on the drug benefit in terms of survival.
目前对于高级别非转移性骨肉瘤的治疗建议包括围手术期化疗和手术。尽管采用了这种强化方案,仍有大约40%的患者会复发。在可切除骨肉瘤的年轻患者中,在辅助细胞毒性化疗中添加免疫调节剂米伐木肽可显著提高6年总生存率(OS),这使其在欧洲和其他国家获得批准。关于其使用的真实世界数据报道非常有限。
我们回顾性评估了在辅助治疗中接受米伐木肽的骨肉瘤患者的数据。数据来自2个大型骨肉瘤中心的医疗记录。本研究的目的是收集希腊关于米伐木肽安全性和有效性的真实世界数据。
我们确定了15例骨肉瘤完全切除且在2015年9月至2020年1月期间接受米伐木肽治疗的患者。诊断时的中位年龄为24岁(16 - 76岁)。骨肉瘤发生在下肢(n = 12)、上肢(n = 2)或髂骨(n = 1)。大多数患者(n = 13)接受顺铂/阿霉素/甲氨蝶呤作为围手术期化疗,其余患者接受顺铂/阿霉素。中位随访46.9个月(范围32.8 - 61.1个月)后,无复发生存期的中位数为58.7个月(范围18.5 - 98.8个月),总生存期的中位数为64.1个月(范围25.6 - 102.6个月)。除发热和寒战外,唯一可能与米伐木肽相关的不良事件是心包炎(n = 1)。
在希腊骨肉瘤患者群体中,包括30岁以上患者,米伐木肽耐受性良好。样本量小和非对照设计不允许就该药物在生存方面的益处得出结论。