Yang Hang, Sun Peng, Wang Yu, Wang Xicheng, Liu Yanyan, Peng Jiyong, Zhou Hui, Li Yajun, Zhang Hong, Hu Jianbing, Zhang Bing, Lin Shunhuan, Yang Chunwei, Li Weidong, Liu Yanping, Ji Meng, Zhao Jinghua, Xue Jianfei, Huang Jiajia, Li Zhiming
Sun Yat-sen University Cancer Center, Guangzhou, PR China.
The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangzhou, PR China.
Oral Oncol. 2025 Mar;162:107211. doi: 10.1016/j.oraloncology.2025.107211. Epub 2025 Feb 13.
Mitoxantrone hydrochloride liposomes (PLM60) have been approved for the treatment of relapsed/refractory peripheral T-cell lymphoma (PTCL) in China. This study evaluated the safety and efficacy of PLM60 in patients with recurrent/metastatic head and neck squamous cell carcinoma (HNSCC).
Patients with histologically confirmed HNSCC (including nasopharyngeal carcinoma (NPC)) were enrolled. PLM60 was administered at a dose of 20 mg/m by intravenous infusion every 21 days (one cycle) with a maximum of eight cycles. The primary objective was to determine the safety and the secondary objective was to assess the efficacy of PLM60 in this setting.
A total of 45 patients with a median age of 50 years were enrolled (26 NPC and 19 non-NPC). Eleven patients completed the planned regimen. The most common hematological adverse events (AEs) were anemia (64.4 %), decreased white blood cell count (55.6 %), and decreased lymphocyte count (46.7 %). The most common non-hematologic AE was skin hyperpigmentation (37.8 %). Grade ≥ 3 AEs occurred in 30 patients (80.0 %), and most were hematologic. Four patients reported AEs leading to death, with two cases assessed as possibly related to the study drug. Of the 37 patients evaluable for efficacy, the overall objective response rate (ORR) was 24.3 % (95 % CI: 11.8-41.2 %) and the disease control rate was 62.2 % (95 % CI: 44.8-77.5 %). The proportion of patients with an overall response was higher in the NPC group (7/25, ORR: 28.0 %) than in the non-NPC group (2/12, ORR: 16.7 %).
PLM60 has demonstrated manageable safety and evidence of efficacy in patients with recurrent/metastatic HNSCC.
盐酸米托蒽醌脂质体(PLM60)在中国已被批准用于治疗复发/难治性外周T细胞淋巴瘤(PTCL)。本研究评估了PLM60在复发/转移性头颈部鳞状细胞癌(HNSCC)患者中的安全性和疗效。
纳入经组织学确诊的HNSCC患者(包括鼻咽癌(NPC))。PLM60以20mg/m²的剂量每21天静脉输注一次(一个周期),最多八个周期。主要目标是确定安全性,次要目标是评估PLM60在此情况下的疗效。
共纳入45例患者,中位年龄50岁(26例NPC和19例非NPC)。11例患者完成了计划方案。最常见的血液学不良事件(AE)为贫血(64.4%)、白细胞计数降低(55.6%)和淋巴细胞计数降低(46.7%)。最常见的非血液学AE为皮肤色素沉着(37.8%)。≥3级AE发生在30例患者中(80.0%),且大多数为血液学事件。4例患者报告AE导致死亡,其中2例评估为可能与研究药物有关。在37例可评估疗效的患者中,总体客观缓解率(ORR)为24.3%(95%CI:11.8 - 41.2%),疾病控制率为62.2%(95%CI:44.8 - 77.5%)。NPC组总体缓解患者的比例(7/25,ORR:28.0%)高于非NPC组(2/12,ORR:16.7%)。
PLM60在复发/转移性HNSCC患者中已显示出可控的安全性和疗效证据。