TY - JOUR
T1 - Long-term follow-up of European APL 2000 trial, evaluating the role of cytarabine combined with ATRA and Daunorubicin in the treatment of nonelderly APL patients
AU - Adès, Lionel
AU - Chevret, Sylvie
AU - Raffoux, Emmanuel
AU - Guerci-Bresler, Agnes
AU - Pigneux, Arnaud
AU - Vey, Nobert
AU - Lamy, Thierry
AU - Huguet, Francoise
AU - Vekhoff, Anne
AU - Lambert, Jean Francois
AU - Lioure, Bruno
AU - de Botton, Stephane
AU - Deconinck, Erick
AU - Ferrant, Augustin
AU - Thomas, Xavier
AU - Quesnel, Bruno
AU - Cassinat, Bruno
AU - Chomienne, Christine
AU - Dombret, Hervé
AU - Degos, Laurent
AU - Fenaux, Pierre
PY - 2013/7/1
Y1 - 2013/7/1
N2 - All-trans retinoic acid (ATRA) combined to anthracycline-based chemotherapy is the reference treatment of acute promyelocytic leukemia (APL). Whereas, in high-risk patients, cytarabine (AraC) is often considered useful in combination with anthracycline to prevent relapse, its usefulness in standard-risk APL is uncertain. In APL 2000 trial, patients with standard-risk APL [i.e., with baseline white blood cell (WBC) count <10,000/mm3] were randomized between treatment with ATRA with Daunorubicin (DNR) and AraC (AraC group) and ATRA with DNR but without AraC (no AraC group). All patients subsequently received combined maintenance treatment. The trial had been prematurely terminated due to significantly more relapses in the no AraC group (J Clin Oncol, (24) 2006, 5703-10), but follow-up was still relatively short. With long-term follow-up (median 103 months), the 7-year cumulative incidence of relapses was 28.6% in the no AraC group, compared to 12.9% in the AraC group (P = 0.0065). In standard-risk APL, at least when the anthracycline used is DNR, avoiding AraC may lead to an increased risk of relapse suggesting that the need for AraC is regimen-dependent.
AB - All-trans retinoic acid (ATRA) combined to anthracycline-based chemotherapy is the reference treatment of acute promyelocytic leukemia (APL). Whereas, in high-risk patients, cytarabine (AraC) is often considered useful in combination with anthracycline to prevent relapse, its usefulness in standard-risk APL is uncertain. In APL 2000 trial, patients with standard-risk APL [i.e., with baseline white blood cell (WBC) count <10,000/mm3] were randomized between treatment with ATRA with Daunorubicin (DNR) and AraC (AraC group) and ATRA with DNR but without AraC (no AraC group). All patients subsequently received combined maintenance treatment. The trial had been prematurely terminated due to significantly more relapses in the no AraC group (J Clin Oncol, (24) 2006, 5703-10), but follow-up was still relatively short. With long-term follow-up (median 103 months), the 7-year cumulative incidence of relapses was 28.6% in the no AraC group, compared to 12.9% in the AraC group (P = 0.0065). In standard-risk APL, at least when the anthracycline used is DNR, avoiding AraC may lead to an increased risk of relapse suggesting that the need for AraC is regimen-dependent.
UR - http://www.scopus.com/inward/record.url?scp=84879409297&partnerID=8YFLogxK
U2 - 10.1002/ajh.23451
DO - 10.1002/ajh.23451
M3 - Article
C2 - 23564205
AN - SCOPUS:84879409297
SN - 0361-8609
VL - 88
SP - 556
EP - 559
JO - American Journal of Hematology
JF - American Journal of Hematology
IS - 7
ER -