Garaventa A, Rondelli R, Lanino E, Dallorso S, Dini G, Bonetti F, Arrighini A, Santoro N, Rossetti F, Miniero R, Andolina M, Amici A, Indolfi P, Lo Curto M, Favre C, Paolucci P, Pession A, De Bernardi B
Department of Hematology-Oncology, Giannina Gaslini Children's Hospital, Genova, Italy.
Bone Marrow Transplant. 1996 Jul;18(1):125-30.
This study reports a large cooperative experience in myeloablative therapy and bone marrow rescue undertaken to define better the outcome of children with disseminated neuroblastoma after megatherapy. Between 1984 and 1993, 135 children underwent myeloablative therapy with bone marrow transplantation (BMT) in nine Italian Centres. One hundred and seventeen children received unpurged autologous BMT, five allogeneic BMT and 13 peripheral blood progenitor cells as rescue. Of these 135 children, 57 were in 1st CR, 11 in 2nd or subsequent CR, 42 in 1st PR, and 25 had more advanced disease. Twelve children (9%) died of toxicity, 86 relapsed or progressed at 1-68 months (median 7 months) and 80 of these subsequently died of progressive disease. Forty-three children are still alive with 37 in continuous remission at a median of 65 months (30-123 months) after BMT. Overall and disease-free survival at 8 years are 28.5% (s.e. 4.3) and 26% (s.e. 4), respectively. Disease-free survival is 34.6% (s.e. 6.7) for the patients grafted in 1st complete remission, 23.6% (s.e. 6.6) for patients grafted in 1st partial remission, 36.4% (s.e. 14.5) for patients grafted in 2nd or subsequent CR, and 8% (5.4) for patients with advanced disease. We conclude these data confirm that early toxicity of myeloablative therapy is manageable and that myeloablative therapy with bone marrow rescue may contribute to an improved long-term survival of children with disseminated neuroblastoma but the objective of cure of all patients remains distant.
本研究报告了在大剂量化疗后进行清髓性治疗和骨髓挽救方面的一项大型合作经验,目的是更好地明确播散性神经母细胞瘤患儿在接受大剂量治疗后的预后情况。1984年至1993年间,135名儿童在意大利的9个中心接受了清髓性治疗及骨髓移植(BMT)。117名儿童接受了未净化的自体BMT,5名接受了异基因BMT,13名接受了外周血祖细胞作为挽救治疗。在这135名儿童中,57名处于首次完全缓解(CR)期,11名处于第二次或后续CR期,42名处于首次部分缓解(PR)期,25名病情更严重。12名儿童(9%)死于毒性反应,86名在1至68个月(中位时间7个月)时复发或病情进展,其中80名随后死于疾病进展。43名儿童仍然存活,37名处于持续缓解状态,BMT后中位时间为65个月(30至123个月)。8年时的总生存率和无病生存率分别为28.5%(标准误4.3)和26%(标准误4)。首次完全缓解期接受移植的患者无病生存率为34.6%(标准误6.7),首次部分缓解期接受移植的患者为23.6%(标准误6.6),第二次或后续CR期接受移植的患者为36.4%(标准误14.5),病情严重的患者为8%(标准误5.4)。我们得出结论,这些数据证实清髓性治疗的早期毒性是可控的,清髓性治疗及骨髓挽救可能有助于提高播散性神经母细胞瘤患儿的长期生存率,但治愈所有患者的目标仍很遥远。