Helson L
Am J Pediatr Hematol Oncol. 1985 Spring;7(1):45-50.
Patients with disseminated neuroblastoma are considered a poor-risk category, hence, our approach towards their treatment should be reconsidered in terms of the unique clinical and biological characteristics of neuroblastoma tumor growth. To this end, we have devised a treatment program consisting of surgery, and a schedule of sequentially escalating doses of cyclophosphamide combined with other drugs until a minimal disease status is obtained. When this is achieved, the patient is treated with maximal therapy, i.e., total body irradiation, high-dose L-phenylalanine mustard and dianhydrogalactitol followed by reconstitution with an autologous bone marrow graft. Details of this program include problems associated with evaluation of response, i.e., evaluation of risk, determination of minimal tumor burden, avoidance of toxicity, and compensation for supportive measures during maximal therapy. Additional problems of purging bone marrow of tumor cells are considered.
播散性神经母细胞瘤患者被视为高危类别,因此,鉴于神经母细胞瘤肿瘤生长独特的临床和生物学特征,我们应重新考虑对其的治疗方法。为此,我们制定了一个治疗方案,包括手术以及一个逐步递增剂量的环磷酰胺联合其他药物的时间表,直至达到最小疾病状态。当达到这一状态时,患者接受强化治疗,即全身照射、高剂量左旋苯丙氨酸氮芥和二去水半乳糖醇,随后进行自体骨髓移植重建。该方案的细节包括与反应评估相关的问题,即风险评估、最小肿瘤负荷的确定、毒性的避免以及强化治疗期间支持措施的补充。还考虑了清除骨髓中肿瘤细胞的其他问题。