TY - JOUR
T1 - Patient stratification based on prednisolone-vincristine-asparaginase resistance profiles in children with acute lymphoblastic leukemia
AU - Den Boer, M L
AU - Harms, D O
AU - Pieters, R
AU - Kazemier, K M
AU - Gobel, U
AU - Körholz, D
AU - Graubner, U
AU - Haas, R J
AU - Jorch, N
AU - Spaar, H J
AU - Kaspers, G J L
AU - Kamps, W A
AU - Van der Does-Van den Berg, A
AU - Van Wering, E R
AU - Veerman, A J P
AU - Janka-Schaub, G E
PY - 2003/9/1
Y1 - 2003/9/1
N2 - PURPOSE: To confirm the prognostic value of a drug resistance profile combining prednisolone, vincristine, and l-asparaginase (PVA) cytotoxicity in an independent group of children with acute lymphoblastic leukemia (ALL) treated with a different protocol and analyzed at longer follow-up compared with our previous study of patients treated according to the Dutch Childhood Leukemia Study Group (DCLSG) ALL VII/VIII protocol.PATIENTS AND METHODS: Drug resistance profiles were determined in 202 children (aged 1 to 18 years) with newly diagnosed ALL who were treated according to the German Cooperative Study Group for Childhood Acute Lymphoblastic Leukemia (COALL)-92 protocol.RESULTS: At a median follow-up of 6.2 years (range, 4.1 to 9.3 years), the 5-year disease-free survival probability (pDFS) rate +/- SE was 69% +/- 7.0%, 83% +/- 4.4%, and 84% +/- 6.8% for patients with resistant (PVA score 7 to 9), intermediate-sensitive (PVA score 5 to 6), and sensitive (SPVA score 3 to 4) profiles, respectively (sensitive and intermediate-sensitive v resistant, P </=.05). Resistant patients were at increased risk of an early event (nonresponse or relapse within 2.5 years of diagnosis) compared with sensitive and intermediate-sensitive patients (P =.03). The profile did not identify patients at higher risk of late relapse, which was also observed for DCLSG ALL-VII/VIII patients now analyzed at a median of 7.5 years of follow-up (range, 4.4 to 10.8 years). Despite being nondiscriminative for late relapses, the resistant profile was still the strongest prognostic factor for COALL-92 patients in a multivariate analysis including known risk factors (P =.07).CONCLUSION: Drug resistance profiles identify patients at higher risk of early treatment failures and may, therefore, be used to improve risk-group stratification of children with ALL.
AB - PURPOSE: To confirm the prognostic value of a drug resistance profile combining prednisolone, vincristine, and l-asparaginase (PVA) cytotoxicity in an independent group of children with acute lymphoblastic leukemia (ALL) treated with a different protocol and analyzed at longer follow-up compared with our previous study of patients treated according to the Dutch Childhood Leukemia Study Group (DCLSG) ALL VII/VIII protocol.PATIENTS AND METHODS: Drug resistance profiles were determined in 202 children (aged 1 to 18 years) with newly diagnosed ALL who were treated according to the German Cooperative Study Group for Childhood Acute Lymphoblastic Leukemia (COALL)-92 protocol.RESULTS: At a median follow-up of 6.2 years (range, 4.1 to 9.3 years), the 5-year disease-free survival probability (pDFS) rate +/- SE was 69% +/- 7.0%, 83% +/- 4.4%, and 84% +/- 6.8% for patients with resistant (PVA score 7 to 9), intermediate-sensitive (PVA score 5 to 6), and sensitive (SPVA score 3 to 4) profiles, respectively (sensitive and intermediate-sensitive v resistant, P </=.05). Resistant patients were at increased risk of an early event (nonresponse or relapse within 2.5 years of diagnosis) compared with sensitive and intermediate-sensitive patients (P =.03). The profile did not identify patients at higher risk of late relapse, which was also observed for DCLSG ALL-VII/VIII patients now analyzed at a median of 7.5 years of follow-up (range, 4.4 to 10.8 years). Despite being nondiscriminative for late relapses, the resistant profile was still the strongest prognostic factor for COALL-92 patients in a multivariate analysis including known risk factors (P =.07).CONCLUSION: Drug resistance profiles identify patients at higher risk of early treatment failures and may, therefore, be used to improve risk-group stratification of children with ALL.
KW - Adolescent
KW - Antineoplastic Agents, Hormonal/administration & dosage
KW - Antineoplastic Agents, Phytogenic/administration & dosage
KW - Antineoplastic Combined Chemotherapy Protocols/therapeutic use
KW - Asparaginase/administration & dosage
KW - Chi-Square Distribution
KW - Child
KW - Child, Preschool
KW - Disease-Free Survival
KW - Drug Resistance, Multiple
KW - Drug Resistance, Neoplasm
KW - Drug Screening Assays, Antitumor/standards
KW - Female
KW - Humans
KW - Infant
KW - Male
KW - Patient Selection
KW - Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy
KW - Predictive Value of Tests
KW - Prednisolone/administration & dosage
KW - Risk
KW - Statistics, Nonparametric
KW - Vincristine/administration & dosage
U2 - 10.1200/JCO.2003.11.031
DO - 10.1200/JCO.2003.11.031
M3 - Article
C2 - 12947061
SN - 0732-183X
VL - 21
SP - 3262
EP - 3268
JO - Journal of clinical oncology : official journal of the American Society of Clinical Oncology
JF - Journal of clinical oncology : official journal of the American Society of Clinical Oncology
IS - 17
ER -