作者
Peipei Ye,Yixuan Cheng,Jiaying Lian,Hongyan Tong,Linjie Li,Qunyi Guo,Wei‐Guo Zhu,Weiying Feng,Li Huang,Lihong Shou,Dong Chen,Xuhui Liu,Shuangyue Li,Xiaohong Du,Min Yang,Wenjuan Yu,Jiejing Qian,Chao Hu,Huafeng Wang,Yangjin Jin,Jian Shen,Hong Pan,Renzhi Pei,Jie Jin,Ying Lu
摘要
Summary A chemotherapy‐based mobilization regimen in patients who mobilize poorly, based on etoposide, cytarabine and pegfilgrastim (EAP), has recently been introduced. The aim of this prospective study was to investigate the efficacy and safety of the EAP regimen in patients with poorly mobilizing multiple myeloma (MM) or lymphoma. This single‐arm clinical trial was performed at eight public hospitals in China and was registered as a clinical trial (NCT05510089). The inclusion criteria were; (1) diagnosis of MM or lymphoma, (2) defined as a ‘poor mobilizer’ and (3) aged 18–75 years. The EAP regimen consisted of etoposide 75 mg/m 2 /day on days 1–2, cytarabine 300 mg/m 2 every 12 h on days 1–2 and pegfilgrastim 6 mg on day 6. The primary endpoint of the study was the ratio of patients achieving adequate mobilization (≥2.0 × 10 6 CD34 + cells/kg). From 1 September 2022 to 15 August 2023, a total of 58 patients were enrolled, 53 (91.4%) achieved adequate mobilization, while 41 (70.7%) achieved optimal mobilization with a median number of cumulative collected CD34 + cells was 9.2 (range 2.1–92.7) × 10 6 /kg and the median number of apheresis per patient of 1.2. The median time from administration of the EAP regimen to the first apheresis was 12 days. Approximately 8.6% of patients required plerixa for rescue, which was successful. Twelve (20.7%) of the 58 patients suffered grade 2–3 infections, while 25 (43.1%) required platelet transfusions. The duration of neutrophil and platelet engraftment was 11 days. In conclusion, these results suggest that the EAP mobilization regimen might be a promising option for poorly mobilizing patients with MM or lymphoma.