Schumacher-Kuckelkorn Roswitha, Hero Barbara, Ernestus Karen, Berthold Frank
Childrens Hospital, Department of Pediatric Oncology and Hematology, University of Cologne, Germany.
Pediatr Blood Cancer. 2005 Aug;45(2):195-201. doi: 10.1002/pbc.20301.
Immunocytological bone marrow assessment for contamination with neuroblastoma cells is based on their characteristic GD2 surface staining. Neuroblastoma without GD2 expression have been rarely and only after antibody therapy reported. Conventional cytology was performed using Pappenheim staining. For immunocytology, the APAAP method was utilized with the 14G2a anti-GD2 mouse monoclonal antibody. 7 x 10(5) cells on cytospin preparations were investigated. In 2003, 288 bone marrow samples from 191 neuroblastoma patients were investigated by cytology and immunocytology. Three cases demonstrated GD2 negativity on cytologically unambiguous neuroblastoma cells. Two female cases (94 and 37 months of age) with stage 4 neuroblastoma had GD2 expressing neuroblastoma cells in bone marrow at diagnosis. At 2nd relapse 25 and 23 months after diagnosis and 8 months and 12 months after anti-GD2 antibody treatment (ch14.18), the bone marrow infiltrating neuroblastoma cells lacked GD2 staining. The third patient, a 63-month-old girl with bone marrow replacement by neuroblastoma cells showed at diagnosis a mixture of GD2-unstained tumor clumps and very weakly stained neuroblastoma cells. Neuroblastoma cells may lack GD2 expression at diagnosis and at recurrence. This observation has diagnostic and therapeutic implications.
用于评估骨髓是否被神经母细胞瘤细胞污染的免疫细胞学法是基于神经母细胞瘤细胞特征性的GD2表面染色。无GD2表达的神经母细胞瘤极为罕见,且仅有在抗体治疗后才有报道。常规细胞学检查采用帕彭海姆染色法。免疫细胞学法采用APAAP法及14G2a抗GD2小鼠单克隆抗体。对细胞涂片制备上的7×10⁵个细胞进行研究。2003年,对191例神经母细胞瘤患者的288份骨髓样本进行了细胞学和免疫细胞学检查。3例在细胞学上明确为神经母细胞瘤的细胞显示GD2阴性。2例4期神经母细胞瘤女性患者(年龄分别为94个月和37个月)在诊断时骨髓中有表达GD2的神经母细胞瘤细胞。在诊断后第2次复发时,即诊断后25个月和23个月以及抗GD2抗体治疗(ch14.18)后8个月和12个月,骨髓浸润的神经母细胞瘤细胞缺乏GD2染色。第3例患者是一名63个月大的女孩,其骨髓被神经母细胞瘤细胞替代,诊断时显示为GD2未染色的肿瘤团块和染色极淡的神经母细胞瘤细胞的混合物。神经母细胞瘤细胞在诊断时和复发时可能缺乏GD2表达。这一观察结果具有诊断和治疗意义。