Pizer B, Papanastassiou V, Hancock J, Cassano W, Coakham H, Kemshead J
Imperial Cancer Research Fund, Paediatric and Neuro-Oncology Group Frenchay Hospital, Bristol.
Br J Haematol. 1991 Apr;77(4):466-72. doi: 10.1111/j.1365-2141.1991.tb08611.x.
A pilot study was performed to investigate the toxicity, pharmacokinetics and therapeutic effect of intrathecally administered radiolabelled monoclonal antibody (MAb) in patients with meningeal acute lymphoblastic leukaemia (ALL). Six children aged 3-16, in second or subsequent central nervous system (CNS) relapse of ALL, received between 629 and 1480 MBq of 131Iodine conjugated to either MAb HD37 (CD19, n = 2) or WCMH15.14 (CD10, n = 4). Conjugate was administered as a single injection either via an Ommaya reservoir (n = 4) or by lumbar puncture (n = 2). Acute toxicity was manifest by headache (n = 4), nausea and vomiting (n = 4) and pyrexia (n = 2). All acute symptoms resolved within 72 h. Transient myelosuppression occurred in three patients. Pharmacokinetic studies included investigation of whole body, blood and CSF clearance of isotope. 131I was seen to clear from the CSF by biexponential kinetics. Five patients responded to therapy. In four, the CSF became clear of blast cells at both 2 and 4 weeks following antibody injection, but evidence of relapse was seen at 6 weeks. The fifth patient, with blast cells present on a cytospin preparation, responded to therapy over an 8-week period but relapsed at 12 weeks. This study demonstrates the potential of targeted radiotherapy in CNS ALL, but further studies are necessary to increase the length of remission.
开展了一项初步研究,以调查鞘内注射放射性标记单克隆抗体(MAb)对脑膜急性淋巴细胞白血病(ALL)患者的毒性、药代动力学和治疗效果。6名年龄在3至16岁之间、处于ALL第二次或后续中枢神经系统(CNS)复发阶段的儿童,接受了629至1480 MBq与MAb HD37(CD19,n = 2)或WCMH15.14(CD10,n = 4)偶联的131碘。偶联物通过奥马亚贮器(n = 4)或腰椎穿刺(n = 2)单次注射给药。急性毒性表现为头痛(n = 4)、恶心和呕吐(n = 4)以及发热(n = 2)。所有急性症状均在72小时内缓解。3名患者出现短暂性骨髓抑制。药代动力学研究包括对同位素的全身、血液和脑脊液清除情况的调查。131I从脑脊液中以双指数动力学清除。5名患者对治疗有反应。4名患者在抗体注射后2周和4周时脑脊液中的原始细胞消失,但在6周时出现复发迹象。第五名患者的细胞涂片制备中有原始细胞,在8周的治疗期内有反应,但在12周时复发。这项研究证明了靶向放疗在中枢神经系统ALL中的潜力,但需要进一步研究以延长缓解期。