Hero B, Hunneman D H, Gahr M, Berthold F
Children's Hospital of the University of Cologne, Köln, Germany.
Med Pediatr Oncol. 2001 Jan;36(1):220-3. doi: 10.1002/1096-911X(20010101)36:1<220::AID-MPO1053>3.0.CO;2-6.
The early biological response has been proved an excellent predictor in acute lymphoblastic leukemia and nephroblastoma. We asked whether catecholamine metabolites, mIBG scan, and bone marrow evaluation might be relevant response markers in disseminated neuroblastoma.
Three hundred sixty-seven unselected stage 4 neuroblastoma patients treated according the German cooperative trial NB90 were entered into the study. Catecholamine plasma and urine levels were centrally determined by gas chromatography/ mass spectrometry. Bone marrow cytology and mIBG scans were evaluated by local investigators.
At diagnosis, mIBG scan was positive in 306 patients (92%), borderline in seven patients (2%), and negative in 19 patients (6%). Bone marrow aspirates were cytologically positive in 292 patients (84%) and negative in 57 patients (16%). Plasma catecholamine levels were elevated in 79% (206 of 260 patients.), urinary levels in 91% (307 of 338 patients). The outcome of patients with normalized mIBG scan after four courses of chemotherapy [5 year EFS (event free survival) 0.22 +/- 0.07] was not superior to the outcome of patients with still abnormal uptake (5 year EFS 0.30 +/- 0.05). The event free survival of patients with still positive bone marrow aspirates after four courses (0.16 +/- 0.06) was inferior to the EFS of patients with negative bone marrow aspirates (0.26 +/- 0.04, P = 0.0054). Urinary catecholamine normalization after four cycles of chemotherapy (5 year EFS 0.35 +/- 0.06 versus 0.26 +/- 0.10) had no influence on outcome, whereas plasma catecholamine normalization after the first (5 year EFS 0.40 +/- 0.09 versus 0.14 +/- 0.07, P= 0.0364) or the fourth cycle (5 year EFS 0.35 +/- 0.06 versus 0.26 +/- 0.10, P = 0.0242) indicated a better outcome.
These data show that serial plasma catecholamine levels and bone marrow aspirates in the course of the disease are useful tools in predicting outcome.
早期生物学反应已被证明是急性淋巴细胞白血病和肾母细胞瘤的良好预测指标。我们探讨了儿茶酚胺代谢产物、间碘苄胍(mIBG)扫描和骨髓评估是否可能是播散性神经母细胞瘤的相关反应标志物。
根据德国合作试验NB90接受治疗的367例未经选择的4期神经母细胞瘤患者纳入本研究。通过气相色谱/质谱法集中测定血浆和尿液中的儿茶酚胺水平。骨髓细胞学检查和mIBG扫描由当地研究人员进行评估。
诊断时,mIBG扫描阳性306例(92%),临界7例(2%),阴性19例(6%)。骨髓穿刺细胞学检查阳性292例(84%),阴性57例(16%)。260例患者中有79%(206例)血浆儿茶酚胺水平升高,338例患者中有91%(307例)尿液儿茶酚胺水平升高。化疗四个疗程后mIBG扫描恢复正常的患者的预后[5年无事件生存率(EFS)0.22±0.07]并不优于摄取仍异常的患者(5年EFS 0.30±0.05)。化疗四个疗程后骨髓穿刺仍为阳性的患者的无事件生存率(0.16±0.06)低于骨髓穿刺阴性的患者(0.26±0.04,P = 0.0054)。化疗四个周期后尿液儿茶酚胺恢复正常(5年EFS 0.35±0.06对0.26±0.10)对预后无影响,而第一个疗程(5年EFS 0.40±0.09对0.14±0.07,P = 0.0364)或第四个疗程(5年EFS 0.35±0.06对0.26±0.10,P = 0.0242)后血浆儿茶酚胺恢复正常表明预后较好。
这些数据表明,病程中的系列血浆儿茶酚胺水平和骨髓穿刺是预测预后的有用工具。