TY - JOUR
T1 - Improved outcome of acute promyelocytic leukemia with high WBC counts over the last 15 years
T2 - The European APL group experience
AU - Kelaidi, Charikleia
AU - Chevret, Sylvie
AU - De Botton, Stéphane
AU - Raffoux, Emmanuel
AU - Guerci, Agnès
AU - Thomas, Xavier
AU - Pigneux, Arnaud
AU - Lamy, Thierry
AU - Rigal-Huguet, Françoise
AU - Meyer-Monard, Sandrine
AU - Chevallier, Patrice
AU - Maloisel, Frédéric
AU - Deconinck, Erick
AU - Ferrant, Augustin
AU - Fegueux, Nathalie
AU - Ifrah, Norbert
AU - Sanz, Miguel
AU - Dombret, Hervé
AU - Fenaux, Pierre
AU - Adès, Lionel
PY - 2009/6/1
Y1 - 2009/6/1
N2 - Purpose: Acute promyelocytic leukemia (APL) with pretreatment WBC counts greater than 10,000/μL is still considered to carry a poorer prognosis than APL with WBC lower than 10,000/mL. We evaluated outcome improvement in such patients in recent years. Patients and Methods: Nine hundred two patients with APL, including 204 patients and 68 patients with WBC counts more than 10,000/μL and more than 50,000/μL, respectively, were enrolled between 1993 and 2005 in two successive randomized trials of the European APL group (APL 93 and APL 2000) that tested, in particular, the modalities of combination of all-trans retinoic acid (ATRA) and chemotherapy, maintenance treatment, escalating doses of cytarabine, early administration of dexamethasone, and CNS prophylaxis. Results: Between the APL 93 and 2000 trials, the complete response (CR) rate increased from 89.6% to 93%, and the 5-year cumulative incidence of relapse (CIR) decreased from 40% to 9.5% in patients with WBC counts of 10,000 to 50,000/μL. In patients with WBC counts more than 50,000/μL, the CR rate increased from 82% to 91%, and 5-year CIR decreased from 59% to 24%. Whereas in the APL 93 trial, increased WBC counts were significantly associated with higher CIR and shorter survival, this was not the case in the APL 2000 trial. In patients with increased WBC counts, enrollment onto the APL 2000 trial (v APL 93) and combined maintenance with ATRA and chemotherapy were associated with significantly lower CIR and better survival. Conclusion: Outcome of APL with high WBC count has markedly improved over the years as a result of fewer early deaths and fewer relapses. Better initial supportive care and combined maintenance treatment have contributed to this improvement.
AB - Purpose: Acute promyelocytic leukemia (APL) with pretreatment WBC counts greater than 10,000/μL is still considered to carry a poorer prognosis than APL with WBC lower than 10,000/mL. We evaluated outcome improvement in such patients in recent years. Patients and Methods: Nine hundred two patients with APL, including 204 patients and 68 patients with WBC counts more than 10,000/μL and more than 50,000/μL, respectively, were enrolled between 1993 and 2005 in two successive randomized trials of the European APL group (APL 93 and APL 2000) that tested, in particular, the modalities of combination of all-trans retinoic acid (ATRA) and chemotherapy, maintenance treatment, escalating doses of cytarabine, early administration of dexamethasone, and CNS prophylaxis. Results: Between the APL 93 and 2000 trials, the complete response (CR) rate increased from 89.6% to 93%, and the 5-year cumulative incidence of relapse (CIR) decreased from 40% to 9.5% in patients with WBC counts of 10,000 to 50,000/μL. In patients with WBC counts more than 50,000/μL, the CR rate increased from 82% to 91%, and 5-year CIR decreased from 59% to 24%. Whereas in the APL 93 trial, increased WBC counts were significantly associated with higher CIR and shorter survival, this was not the case in the APL 2000 trial. In patients with increased WBC counts, enrollment onto the APL 2000 trial (v APL 93) and combined maintenance with ATRA and chemotherapy were associated with significantly lower CIR and better survival. Conclusion: Outcome of APL with high WBC count has markedly improved over the years as a result of fewer early deaths and fewer relapses. Better initial supportive care and combined maintenance treatment have contributed to this improvement.
UR - http://www.scopus.com/inward/record.url?scp=66849103735&partnerID=8YFLogxK
U2 - 10.1200/JCO.2008.18.4119
DO - 10.1200/JCO.2008.18.4119
M3 - Article
C2 - 19414681
AN - SCOPUS:66849103735
SN - 0732-183X
VL - 27
SP - 2668
EP - 2676
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 16
ER -