TY - JOUR
T1 - High cumulative rate of secondary leukemia after continuous etoposide treatment for solid tumors in children and young adults
AU - Le Deley, Marie Cécile
AU - Vassal, Gilles
AU - Taïbi, Ahmed
AU - Shamsaldin, Akthar
AU - Leblanc, Thierry
AU - Hartmann, Olivier
PY - 2005/7/1
Y1 - 2005/7/1
N2 - Background. In a national pediatric case-control study, we observed a very high relative risk of leukemia in patients who had received continuous etoposide (CE) over 6 months or more, but we could not estimate the absolute risk. The purpose of the present study was to estimate this absolute risk after CE. Procedures. We report a study of 18 patients with refractory or recurrent tumors who received CE over 6 months or more between 1995 and 1997. It was administered either 3 days a week for 3/4 weeks (″3 × 3″, 14 patients) or 7 days a week for 3/4 weeks (″7 × 3″, four patients). Results. Five patients developed secondary leukemia 10-25 months after the initiation of CE. All the others died of their first tumor. The cumulative incidence of leukemia at 30 months was 28% (95% CI, 10%-53%). A chromosome 11q23 rearrangement was found in 3/5 cases. All four patients who received the ″7 × 3″ CE schedule developed leukemia compared to 1/14 treated with the ″3 × 3″ CE schedule (P = 0.002). Conclusions. Given its efficacy, CE may still have a place as a palliative treatment. However, the risk of leukemia must be borne in mind when considering its use in patients with a better prognosis.
AB - Background. In a national pediatric case-control study, we observed a very high relative risk of leukemia in patients who had received continuous etoposide (CE) over 6 months or more, but we could not estimate the absolute risk. The purpose of the present study was to estimate this absolute risk after CE. Procedures. We report a study of 18 patients with refractory or recurrent tumors who received CE over 6 months or more between 1995 and 1997. It was administered either 3 days a week for 3/4 weeks (″3 × 3″, 14 patients) or 7 days a week for 3/4 weeks (″7 × 3″, four patients). Results. Five patients developed secondary leukemia 10-25 months after the initiation of CE. All the others died of their first tumor. The cumulative incidence of leukemia at 30 months was 28% (95% CI, 10%-53%). A chromosome 11q23 rearrangement was found in 3/5 cases. All four patients who received the ″7 × 3″ CE schedule developed leukemia compared to 1/14 treated with the ″3 × 3″ CE schedule (P = 0.002). Conclusions. Given its efficacy, CE may still have a place as a palliative treatment. However, the risk of leukemia must be borne in mind when considering its use in patients with a better prognosis.
KW - Child
KW - Continuous etoposide
KW - Etoposide
KW - Schedule
KW - Secondary leukemia
KW - Therapy-related leukemia
UR - http://www.scopus.com/inward/record.url?scp=20344374970&partnerID=8YFLogxK
U2 - 10.1002/pbc.20380
DO - 10.1002/pbc.20380
M3 - Article
C2 - 15795880
AN - SCOPUS:20344374970
SN - 1545-5009
VL - 45
SP - 25
EP - 31
JO - Pediatric Blood and Cancer
JF - Pediatric Blood and Cancer
IS - 1
ER -