TY - JOUR
T1 - In vitro anthracycline cross-resistance pattern in childhood acute lymphoblastic leukaemia
AU - Klumper, E
AU - Pieters, R
AU - den Boer, M L
AU - Huismans, D R
AU - Loonen, A H
AU - Veerman, A J
N1 - Funding Information:
This work was supported by Grants IKA 90-05 and VU 93-641 from the Dutch Cancer Society. We thank the members of the German COALL-group (Head: Professor G. Janka-Schaub. Hamburg) and the relapse section of the German BFM-group (Head: Professor G. Henze. Berlin) for providing patient samples. We thank G. McLean for editorial assistance.
PY - 1995/6
Y1 - 1995/6
N2 - Daunorubicin (DNR) is a major front-line drug in the treatment of childhood acute lymphoblastic leukaemia (ALL). Previously, we showed that in vitro resistance to DNR at diagnosis is related to a poor long-term clinical outcome in childhood ALL and that relapsed ALL samples are more resistant to DNR than untreated ALL samples. In cell line studies, idarubicin (IDR), aclarubicin (ACR) and mitoxantrone (MIT) showed a (partial) lack of cross-resistance to the conventional anthracyclines DNR and doxorubicin (DOX), but clinical studies in childhood ALL have been inconclusive about the suggested lack of cross-resistance. In the present study we determined the in vitro cross-resistance pattern between DNR, DOX, IDR, ACR and MIT in 48 untreated and 39 relapsed samples from children with ALL using the MTT assay. The relapsed ALL group was about twice as resistant to DNR, DOX, IDR, ACR and MTT as the untreated ALL group. Thus, resistance developed to all five drugs. We found a significant cross-resistance between DNR, DOX, IDR, ACR and MIT, although in some individual cases in vitro anthracycline cross-resistance was less pronounced. We conclude that IDR, ACR and MIT cannot circumvent in vitro resistance to DNR in childhood ALL. Clinical studies may still prove whether IDR, ACR or MIT has a more favourable toxicity profile than DNR.
AB - Daunorubicin (DNR) is a major front-line drug in the treatment of childhood acute lymphoblastic leukaemia (ALL). Previously, we showed that in vitro resistance to DNR at diagnosis is related to a poor long-term clinical outcome in childhood ALL and that relapsed ALL samples are more resistant to DNR than untreated ALL samples. In cell line studies, idarubicin (IDR), aclarubicin (ACR) and mitoxantrone (MIT) showed a (partial) lack of cross-resistance to the conventional anthracyclines DNR and doxorubicin (DOX), but clinical studies in childhood ALL have been inconclusive about the suggested lack of cross-resistance. In the present study we determined the in vitro cross-resistance pattern between DNR, DOX, IDR, ACR and MIT in 48 untreated and 39 relapsed samples from children with ALL using the MTT assay. The relapsed ALL group was about twice as resistant to DNR, DOX, IDR, ACR and MTT as the untreated ALL group. Thus, resistance developed to all five drugs. We found a significant cross-resistance between DNR, DOX, IDR, ACR and MIT, although in some individual cases in vitro anthracycline cross-resistance was less pronounced. We conclude that IDR, ACR and MIT cannot circumvent in vitro resistance to DNR in childhood ALL. Clinical studies may still prove whether IDR, ACR or MIT has a more favourable toxicity profile than DNR.
KW - Aclarubicin/therapeutic use
KW - Antibiotics, Antineoplastic/therapeutic use
KW - Bone Marrow/pathology
KW - Child
KW - Daunorubicin/therapeutic use
KW - Dose-Response Relationship, Drug
KW - Drug Resistance
KW - Humans
KW - Idarubicin/therapeutic use
KW - Mitoxantrone/therapeutic use
KW - Precursor Cell Lymphoblastic Leukemia-Lymphoma/blood
KW - Recurrence
UR - http://www.scopus.com/inward/record.url?scp=0029038296&partnerID=8YFLogxK
U2 - 10.1038/bjc.1995.231
DO - 10.1038/bjc.1995.231
M3 - Article
C2 - 7779709
SN - 0007-0920
VL - 71
SP - 1188
EP - 1193
JO - British journal of cancer
JF - British journal of cancer
IS - 6
ER -