Frappaz D, Perol D, Michon J, Berger C, Coze C, Bernard J L, Zucker J M, Philip T
Department of Pediatrics, Centre Léon Bérard, 28 rue Laënnec, Lyon, 69373, France.
Br J Cancer. 2002 Nov 18;87(11):1197-203. doi: 10.1038/sj.bjc.6600627.
The Lyon-Marseille-Curie-Est (LMCE) of France cooperative group has previously reported successive series of unselected stage four children older than 1 year at diagnosis with metastatic neuroblastoma (LMCE 1 and 3). The goal of LMCE 5 study was to increase progression free survival rate as compared to LMCE 1 and 3. Based on improvements reported with post induction chemotherapy, the LMCE 5 used post induction for all children, but omitted total body irradiation and immunomagnetic purging in megatherapy regimen for all children. Twenty-five sequentially diagnosed children received an induction regimen which compared with previous induction included an increased dose of etoposide and cyclophosphamide, delivered similar dose of cisplatinum, and deleted doxorubicin and vincristin. After surgery treatment was stratified based on response and eligible children received etoposide carboplatin (LMCE 5A : n=10)+/-doxorubicin (LMCE 5B-C n=13) followed by megatherapy (melphalan without total body irradiation and unpurged peripheral blood stem cell rescue). The increase in drug doses during induction did not improve remission rate. The progression free survival at 6 years is 8%. It is significantly worse than LMCE 3, and equivalent to LMCE 1 study though toxic death rate has decreased with increasing experience. Failure to improve the response rate during induction and reducing the megatherapy regimen may be the main factors in this disappointing result. Modified strategies for induction, non toxic alternative to total body irradiation, and post megatherapy regimen should be developed.
法国里昂-马赛-居里-东部(LMCE)合作组先前报告了一系列未经挑选的、诊断时年龄超过1岁的转移性神经母细胞瘤四期患儿(LMCE 1和3)。LMCE 5研究的目标是与LMCE 1和3相比提高无进展生存率。基于诱导化疗后报告的改善情况,LMCE 5对所有患儿采用诱导后治疗,但在大剂量化疗方案中省略了全身照射和免疫磁珠净化。25例序贯诊断的患儿接受了一种诱导方案,与先前的诱导方案相比,该方案增加了依托泊苷和环磷酰胺的剂量,顺铂剂量相似,且删除了多柔比星和长春新碱。手术后,根据反应进行分层治疗,符合条件的患儿接受依托泊苷联合卡铂(LMCE 5A:n = 10)±多柔比星(LMCE 5B - C,n = 13),随后进行大剂量化疗(美法仑,无全身照射和未净化的外周血干细胞救援)。诱导期间药物剂量的增加并未提高缓解率。6年时的无进展生存率为8%。这明显比LMCE 3差,尽管随着经验的增加毒性死亡率有所下降,但与LMCE 1研究相当。诱导期间未能提高反应率以及减少大剂量化疗方案可能是导致这一令人失望结果的主要因素。应该制定改进的诱导策略、全身照射的无毒替代方法以及大剂量化疗后的方案。