INDUCTION TOXICITY OF A MODIFIED MEMORIAL-SLOAN-KETTERING-NEW-YORK IIPROTOCOL IN CHILDREN WITH RELAPSED ACUTE LYMPHOBLASTIC-LEUKEMIA - A SINGLE INSTITUTION STUDY
Bj. Morland et Pj. Shaw, INDUCTION TOXICITY OF A MODIFIED MEMORIAL-SLOAN-KETTERING-NEW-YORK IIPROTOCOL IN CHILDREN WITH RELAPSED ACUTE LYMPHOBLASTIC-LEUKEMIA - A SINGLE INSTITUTION STUDY, Medical and pediatric oncology, 27(3), 1996, pp. 139-144
Although the chance of cure for children with acute lymphoblastic leuk
aemia (ALL) is high, their outlook with subsequent relapse is poor. Bo
ne 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 repor
t the experience of using an intensive chemotherapy protocol (Memorial
Sloan-Kettering-New York II Protocol, MSK-NY-II) in a series of relap
sed children with ALL. Thirty children presenting to the Royal Alexand
ra Hospital for Children, Sydney, in their first relapse of ALL were t
reated according to a modification of the original MSK-NY-II protocol.
Three children (10%) died during induction therapy, two from overwhel
ming Cram-negative sepsis, and one from intracerebral haemorrhage. Of
27 children completing induction, two children failed to enter remissi
on; however, both had planned deviations from the protocol. Infectious
complications were prominent with a total of 55 admissions for febril
e neutropenic episodes. Eight children required the support of the int
ensive care unit for infectious complications. A total of 36 microbiol
ogical isolates were obtained from the patients during induction ther
apy. Ten bone marrow transplant procedures have been subsequently perf
ormed in these children, of whom five are alive and disease free at th
e time of writing. The MSK-NY-II protocol is an intensive regimen but
with encouraging early remission rates in relapsed childhood ALL. Earl
y sepsis in previously immunosuppressed children is an important cause
of induction death. (C) 1996 Wiley-Liss, Inc.