Morland B J, Shaw P J
Department of Oncology, Royal Alexandra Hospital for Children, Camperdown, NSW, Australia.
Med Pediatr Oncol. 1996 Sep;27(3):139-44. doi: 10.1002/(SICI)1096-911X(199609)27:3<139::AID-MPO1>3.0.CO;2-F.
Although the chance of cure for children with acute lymphoblastic leukaemia (ALL) is high, their outlook with subsequent relapse is poor. Bone marrow transplantation may be an option for some, but the need for intensive reinduction chemotherapy regimens remains the best hope for effecting cure in the majority of relapsed children. The authors report the experience of using an intensive chemotherapy protocol (Memorial Sloan-Kettering-New York II Protocol, MSK-NY-II) in a series of relapsed children with ALL. Thirty children presenting to the Royal Alexandra Hospital for Children, Sydney, in their first relapse of ALL were treated according to a modification of the original MSK-NY-II protocol. Three children (10%) died during induction therapy, two from overwhelming Gram-negative sepsis, and one from intracerebral haemorrhage. Of 27 children completing induction, two children failed to enter remission; however, both had planned deviations from the protocol. Infectious complications were prominent with a total of 55 admissions for febrile neutropenic episodes. Eight children required the support of the intensive care unit for infectious complications. A total of 36 microbiological isolates were obtained from the patients during induction therapy. Ten bone marrow transplant procedures have been subsequently performed in these children, of whom five are alive and disease free at the time of writing. The MSK-NY-II protocol is an intensive regimen but with encouraging early remission rates in relapsed childhood ALL. Early sepsis in previously immunosuppressed children is an important cause of induction death.
尽管急性淋巴细胞白血病(ALL)患儿的治愈几率很高,但他们后续复发后的预后较差。骨髓移植对部分患儿可能是一种选择,但对于大多数复发患儿而言,采用强化再诱导化疗方案仍是实现治愈的最大希望。作者报告了在一系列复发ALL患儿中使用强化化疗方案(纪念斯隆 - 凯特琳 - 纽约II方案,MSK - NY - II)的经验。30名首次复发ALL的患儿在悉尼皇家亚历山德拉儿童医院接受治疗,治疗方案是对原始MSK - NY - II方案的改良。3名患儿(10%)在诱导治疗期间死亡,2名死于严重革兰氏阴性菌败血症,1名死于脑出血。在27名完成诱导治疗的患儿中,2名未进入缓解期;不过,这两名患儿都有计划外的方案偏离情况。感染并发症较为突出,因发热性中性粒细胞减少发作共入院55次。8名患儿因感染并发症需要重症监护病房的支持。在诱导治疗期间共从患儿身上分离出36株微生物。这些患儿随后共进行了10次骨髓移植手术,截至撰写本文时,其中5名患儿存活且无疾病。MSK - NY - II方案是一种强化方案,但在复发的儿童ALL中早期缓解率令人鼓舞。既往免疫抑制患儿的早期败血症是诱导治疗死亡的重要原因。