OUTCOME AFTER FIRST RELAPSE IN CHILDREN WITH ACUTE LYMPHOBLASTIC-LEUKEMIA - A POPULATION-BASED STUDY OF 315 PATIENTS FROM THE ORDIC-SOCIETY-OF-PEDIATRIC-HEMATOLOGY-AND-ONCOLOGY (NOPHO)
H. Schroeder et al., OUTCOME AFTER FIRST RELAPSE IN CHILDREN WITH ACUTE LYMPHOBLASTIC-LEUKEMIA - A POPULATION-BASED STUDY OF 315 PATIENTS FROM THE ORDIC-SOCIETY-OF-PEDIATRIC-HEMATOLOGY-AND-ONCOLOGY (NOPHO), Medical and pediatric oncology, 25(5), 1995, pp. 372-378
This study reports the outcome after relapse of acute lymphoblastic le
ukemia (ALL) in a population-based study of 809 children over 1 year o
f age diagnosed July 1981 through June 1986 and with non-B acute lymph
oblastic leukemia in the five Nordic countries. By January 1994, 315 c
hildren had suffered at least one relapse. The bone marrow was involve
d in 216 cases. There were 69 isolated CNS relapses, 25 isolated testi
cular recurrences and five relapses in other extramedullary sites. Of
the 315 children with relapse, 94 are still in a second complete remis
sion 12-138 (median: 78) months after relapse. The overall probability
of a second event free survival (P-2.EFS) and survival after relapse
was 0.28 and 0.33 respectively. The probability of remaining in second
remission at 11 years was significantly correlated to the duration of
first remission (P < 0.001), the site of relapse (P < 0.001) and gend
er (P = 0.004). The P-2.EFS for early, intermediate, and late bone mar
row involved relapses were 0.08, 0.19, and 0.50 respectively. For earl
y, intermediate and late isolated CNS relapses the P-2.EFS were 0.21,
0.38 and 0.61, respectively. The P-2.EFS for boys with isolated testic
ular relapses was 0.69. Girls with isolated CNS relapse (P < 0.001) an
d with bone marrow involved relapse (P = 0.04) had a significantly bet
ter prognosis than boys. Children with initial high risk criteria, esp
ecially T-ALL and mediastinal mass who relapsed, had a very poor progn
osis. Conclusion: In this population-based study, about 30% of childre
n with ALL obtained a long second remission and possible cure. (C) 199
5 Wiley-Liss, Inc.