Division of Hematologic Oncology, Lymphoma Service, Memorial Sloan-Kettering Cancer Center, New York, NY.
City of Hope Medical Center, Duarte, CA.
Clin Lymphoma Myeloma Leuk. 2020 Nov;20(11):749-756.e1. doi: 10.1016/j.clml.2019.04.010. Epub 2019 Apr 29.
Mantle-cell lymphoma (MCL) is sensitive to radiotherapy, and the CD20 antigen is relatively highly expressed in MCL. Therefore, radioimmunotherapy using radiolabeled anti-CD20 monoclonal antibodies has the potential to treat MCL. The objective of this study was to investigate the efficacy, pharmacokinetics, and safety of tositumomab (TST) and iodine-131 tositumomab (I-131 TST) followed by 6 cycles of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) in patients with previously untreated MCL (ClinicalTrials.govNCT00022945).
In this phase 2 open-label study, patients received dosimetric (day 0: 450 mg TST, then 35 mg I-131 TST [5 mCi]) and therapeutic (between days 7 and 14: 450 mg TST, then an individualized dose of I-131 TST [65-75 cGy]) TST/I-131 TST, with CHOP treatment commencing approximately 13 weeks after the therapeutic dose. The primary end point was the MCL response rate to treatment; secondary end points included confirmed complete response rate and total body residence time.
Twenty-six patients were enrolled, and 25 were included in the intent-to-treat population. The overall unconfirmed response rate was 84%, and the confirmed complete response rate was 44%. The median progression free-survival was 27.6 months. The median total body residence time was 94.5 hours. No new or unexpected safety signals were identified.
Patients with previously untreated MCL who received radioimmunotherapy with TST/I-131 TST followed by CHOP had a high response rate and a long duration of response, indicating that radioimmunotherapy is a therapeutic option in this patient population.
套细胞淋巴瘤(MCL)对放射治疗敏感,并且 MCL 中相对高度表达 CD20 抗原。因此,使用放射性标记的抗 CD20 单克隆抗体的放射免疫治疗有可能治疗 MCL。本研究的目的是研究未经治疗的 MCL 患者(ClinicalTrials.govNCT00022945)接受托西莫单抗(TST)和碘-131 托西莫单抗(I-131 TST)治疗后进行 6 个周期环磷酰胺、多柔比星、长春新碱和泼尼松(CHOP)治疗的疗效、药代动力学和安全性。
在这项 2 期开放标签研究中,患者接受了剂量测定(第 0 天:450mgTST,然后 35mgI-131 TST[5mCi])和治疗(第 7-14 天:450mgTST,然后个体化剂量 I-131 TST[65-75cGy])TST/I-131 TST,在治疗剂量后约 13 周开始 CHOP 治疗。主要终点是 MCL 对治疗的反应率;次要终点包括确认的完全缓解率和全身停留时间。
共纳入 26 例患者,25 例患者纳入意向治疗人群。未确认的总缓解率为 84%,确认的完全缓解率为 44%。无进展生存的中位数为 27.6 个月。全身停留时间的中位数为 94.5 小时。未发现新的或意外的安全性信号。
接受 TST/I-131 TST 放射免疫治疗后再接受 CHOP 治疗的未经治疗的 MCL 患者具有较高的反应率和较长的缓解持续时间,表明放射免疫治疗是该患者群体的一种治疗选择。