Donfrancesco A, De Bernardi B, Carli M, Mancini A, Nigro M, De Sio L, Casale F, Bagnulo S, Helson L, Deb G
Ospedale Bambino Gesù, Servizio di Oncologia, Roma, Italy.
Eur J Cancer. 1995;31A(4):612-5. doi: 10.1016/0959-8049(95)00068-t.
Based upon phase I and II studies of deferoxamine alone and in combination with cytotoxic agents cyclophosphamide, etoposide, carboplatin, and thiotepa (D-CECaT), we initiated a single arm multicentre trial in 1992 for advanced neuroblastoma. 57 of 65 patients who entered the trial were evaluable. Following 4 courses of the D-CECaT, almost all the patients underwent surgery. Toxicity was moderate and mainly reversible myelosuppression. The post-surgically defined responses in stage 3 high risk, stage 4 moderate risk and stage 4 high risk patients included 24 complete responses, 26 partial responses, and 3 minor responses, and 4 patients had progressive disease. These patients are being followed to determine the impact of this programme on their overall survival.
基于去铁胺单独使用以及与细胞毒性药物环磷酰胺、依托泊苷、卡铂和塞替派联合使用(D - CECaT)的I期和II期研究,我们于1992年针对晚期神经母细胞瘤开展了一项单臂多中心试验。入组试验的65例患者中有57例可评估。在接受4个疗程的D - CECaT治疗后,几乎所有患者都接受了手术。毒性为中度,主要是可逆性骨髓抑制。3期高危、4期中度危险和4期高危患者术后确定的反应包括24例完全缓解、26例部分缓解和3例轻微缓解,4例患者病情进展。这些患者正在接受随访,以确定该方案对其总生存期的影响。