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首页> 外文期刊>Medicine. >Metronomic oral cyclosphosphamide as third-line systemic treatment or beyond in patients with inoperable locoregionally advanced recurrent or metastatic nasopharyngeal carcinoma
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Metronomic oral cyclosphosphamide as third-line systemic treatment or beyond in patients with inoperable locoregionally advanced recurrent or metastatic nasopharyngeal carcinoma

机译:元数值循环亚磷酰胺作为第三线全身治疗或超越患者患者,可致命的型转发鼻咽或转移性鼻咽癌

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There is no standard third-line or further systemic treatment for patients with inoperable locoregionally advanced recurrent or metastatic nasopharyngeal carcinoma (NPC). Metronomic oral cyclophosphamide provides an acceptable and cheap option for these heavily pretreated patients who had limited choices. We conducted a prospective phase II single-arm open-label study of metronomic oral cyclophosphamide. Patients with locoregionally advanced recurrent inoperable (rT3/T4, rN2-N3b) or metastatic (rM1) NPC who had Eastern Cooperative Oncology Group (ECOG) performance status (PS) (0–2) and had progressed after at least 2 lines of palliative systemic chemotherapy were eligible. They received oral cyclophosphamide between 50 and 150 mg once daily until progressive disease or unacceptable toxicity. Objective response rate (ORR), disease control rate (DCR), biochemical response (two consecutive declines of plasma EBV DNA after treatment), progression-free survival (PFS), overall survival (OS), and safety profiles were evaluated. A total of 56 patients were recruited. Thirty-three, 13, 6, 3, and 1 patients received cyclophosphamide as 3rd, 4th, 5th, 6th, and 7th line of therapy respectively. After a median follow-up of 9.95 months (range 1.76–59.51 months), the ORR was 8.9% and the DCR was 57.1%. The median PFS and OS were 4.47 and 9.20 months, respectively. Those with PS 1 had longer median PFS (5.49 months) compared to those with PS 2 (3.75 months, P = .011). Besides, those who had locoregionally recurrent disease had better PFS (8.97 months, 95% CI, 0.53–17.41 months) compared to those who had distant metastases (4.14 months, 95% CI, 2.53–5.75 months, P = .020). Multivariable analysis revealed that PS 1 (vs 2) ( P = .020) and locoregional recurrence (vs metastasis) ( P = .029) were the only significant independent prognostic factors of PFS. Around 16 (28.6%) patients developed grade ≥3 adverse events, including malaise (5.4%), hematological (8.9%), gastrointestinal (3.6%), feverish (3.6%), and hemorrhagic (1.8%) events. The median cost of the whole drug treatment was 51.65 US dollars (USD) (range 4.15–142.75 USD) (1 USD = 7.8 HK dollars [HKD]). Metronomic oral cyclophosphamide is an acceptable third-line or beyond systemic therapy for locoregionally advanced recurrent or metastatic NPC with acceptable toxicity and limited financial burden.
机译:对于型型型型自发性或转移性鼻咽癌(NPC)的患者,没有标准的第三线或进一步的全身治疗。元组织口腔环磷酰胺为这些具有有限有限的预处理患者提供了可接受的和廉价的选择。我们进行了一项预期第二阶段单臂开放标签研究对核心口腔环磷酰胺。患有东方合作肿瘤学组(ECOG)绩效状况(PS)(0-2)的患者患者患者患者(RT3 / T4,RN2-N3B)或转移性(RM1)NPC,并在至少2行的姑息线后进行全身化疗有资格。它们每天一次接受50至150毫克的口服环磷酰胺,直到渐进性疾病或不可接受的毒性。客观响应率(ORR),疾病控制率(DCR),生物化学响应(治疗后的血浆EBV DNA的两个连续下降),评估无进展生存(PFS),总存活(OS)和安全谱。共招募了56名患者。三十三元,13,6,3和1名患者分别接受环磷酰胺,分别为第3,第4,第5次和第7系。在9.95个月的中位随访后(1.76-59.51个月),ORR为8.9%,DCR为57.1%。中位数PFS和OS分别为4.47和9.20个月。与PS 2(3.75个月,P = .011)相比,有PS 1的人具有较长的中位数PFS(5.49个月)。此外,与那些具有远处转移的人(4.14个月,95%CI,2.53-5.75个月,那些患者具有更好的PFS(8.97个月,95%CI,0.53-17.41个月)。多变量分析显示PS 1(VS 2)(P = .020)和型致血液复发(VS转移)(P = .029)是PFS的唯一明显的独立预后因素。大约16名(28.6%)患者患者开发≥3级不良事件,包括萎靡不振(5.4%),血液学(8.9%),胃肠道(3.6%),发烧(3.6%)和出血(1.8%)事件。整个药物治疗的中位数成本为51.65美元(USD)(范围4.15-142.75美元)(1美元= 7.8 HK美元[HKD])。元组织口腔环磷酰胺是一种可接受的第三线或超越全身疗法,用于型型转发或转移性NPC,具有可接受的毒性和金融负担有限。

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