All-trans retinoic acid in acute promyelocytic leukemia:: long-term outcome and prognostic factor analysis from the North American Intergroup protocol

被引:339
|
作者
Tallman, MS
Andersen, JW
Schiffer, CA
Appelbaum, FR
Feusner, JH
Woods, WG
Ogden, A
Weinstein, H
Shepherd, L
Willman, C
Bloomfield, CD
Rowe, JM
Wiernik, PH
机构
[1] Northwestern Univ, Feinburg Sch Med, Dept Med,Div Hematol Oncol, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
[2] Eastern Cooperat Oncol Grp, Brookline, MA USA
[3] Harvard Univ, Sch Publ Hlth, ECOG, Boston, MA 02115 USA
[4] Wayne State Univ, Karmanos Canc Ctr, Detroit, MI USA
[5] Canc & Leukemia Grp B, Chicago, IL USA
[6] Univ Washington, Fred Hutchinson Canc Res Ctr, Seattle, WA 98195 USA
[7] SW Oncol Grp, San Antonio, TX USA
[8] Childrens Hosp No Calif Oakland, Oakland, CA USA
[9] Emory Univ, Childrens Healthcare, Atlanta, GA 30322 USA
[10] Texas Childrens Canc Ctr, Houston, TX USA
[11] Pediat Oncol Grp, Chicago, IL USA
[12] Harvard Univ, Massachusetts Gen Hosp, Sch Med, POG, Boston, MA USA
[13] Natl Canc Inst, Canada Clin Trials Grp, Kingston, ON, Canada
[14] Univ New Mexico, SWOG, Albuquerque, NM 87131 USA
[15] Ohio State Univ, CALGB, Columbus, OH 43210 USA
[16] Technion Israel Inst Technol, Rambam Med Ctr, ECOG, Haifa, Israel
[17] New York Med Coll, Our Lady Mercy Canc Ctr, ECOG, Bronx, NY USA
关键词
D O I
10.1182/blood-2002-02-0632
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We previously reported a benefit for all-trans retinoic acid (ATRA) in both induction and maintenance therapy in patients with acute promyelocytic leukemia (APL). To determine the durability of this benefit and identify important prognostic factors, long-term follow-up of the North American Intergroup APL trial is reported. A total of 350 patients with newly diagnosed APL were randomized to either daunorubicin and cytarabine (DA) or ATRA for induction and then either ATRA maintenance or observation following consolidation chemotherapy. The complete remission (CR) rates were not significantly different between the ATRA and DA groups (70% and 73%, respectively). However, the 5-year disease-free survival (DFS) and overall survival (OS) were longer with ATRA than with DA for induction (69% vs 29% and 69% vs 45%, respectively). Based on both induction and maintenance randomizations, the 5-year DFS was 16% for patients randomized to DA and observation, 47% for DA and ATRA, 55% for ATRA and observation, and 74% for ATRA and ATRA. There was no advantage of either induction regimen among any subgroups when CR alone was considered. However, female sex, classical M3 morphology (vs the microgranular variant [M3v]), and treatment-white blood cell count (WBC) interaction (ATRA/WBC below 2 x 10(9)/L [2000/muL] best, DA/WBC above 2 x 10(9)/L worst) were each significantly associated with improved DFS (P<.05). Treatment with ATRA, WBC below 2 x 10(9)/L, and absence of bleeding disorder were each significantly associated with improved OS. Age more than 15 years, female sex, and treatment-morphology interaction (DA/M3v worst, ATRA best regardless of morphology) were each significantly associated with improved DFS based on maintenance randomization. The improvement in outcome with ATRA in APL was maintained with long-term follow-up.
引用
收藏
页码:4298 / 4302
页数:5
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