Recently, several conditioning regimens did not include total body irradiation (TBI) anymore, especially in the case of young children due to cognitive sequelae and late effects on growth and height. Thus, such effective chemotherapy conditioning regimens were developed to avoid these complications. Busulfan is one of the major drugs used in these treatments, but, is also administered in high dose chemotherapy followed by autograft. In both situations, long term pulmonary side effects were diagnosed in a few cases. Even if the occurrence is not very frequent, the clinical management is a real challenge regarding the reduced quality of life and life expectancy of these patients. Up to now, no correlation was done between respiratory sequelae and busulfan pharmacokinetics. Hence, in the investigators' pediatric onco-hematological unit, a prospective study will begin and last three years to assess the respiratory side effects due to busulfan and their potential links with individual drug pharmacokinetic measures. These results will be compared to patients treated with TBI during the same period of time.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
35
5mg/kg/day (oral route : 4 doses/day for 4 days)
respiratory function tests before allograft or autograft and at several times in the follow up (3, 6, 12, 18 and 24 months).
12 blood collections : * after 1st Busulfan taken : t0; t0 + 30 mn; t0 + 1h; t0 + 2h ; t0 + 3h ; t0 + 4h ; t0 + 5 h. * 3 hours after 2nd taken of Busulfan * 3 hours after 3rd taken of Busulfan * 3 hours after 4th taken of Busulfan * 3 hours after 5th taken of Busulfan * 3 hours after 6th taken of Busulfan.
Service d'Explorations Fonctionelles Respiratoires - Hôpital Civil
Strasbourg, France
RECRUITINGService de Pédiatrie Onco-Hématologie - Hôpital de Hautepierre
Strasbourg, France
RECRUITINGDetermination of respiratory side effect frequency in the two years follow up of allograft or autograft treated with busulfan
Time frame: before allograft or autograft and at several times in the follow up (3, 6, 12, 18 and 24 months).
Comparison to respiratory side effect frequency with TBI conditioning regimen
Time frame: before allograft or autograft and at several times in the follow up (3, 6, 12, 18 and 24 months).
Busulfan pharmacokinetics
Time frame: after 1st Busulfan taken : t0; t0 + 30 mn; t0 + 1h; t0 + 2h ; t0 + 3h ; t0 + 4h ; t0 + 5 h ; 3 h after 2nd Busulfan taken ; 3 hours after 3rd Busulfan taken ; 3 h after 4st Busulfan taken ;3 h after 5st Busulfan taken ;3 h after 6st Busulfan taken
Establish a potential link between respiratory side effects and busulfan pharmacokinetics
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