All-trans retinoic acid/AS2O3 combination yields a high quality remission and survival in newly diagnosed acute promyelocytic leukemia

被引:490
作者
Shen, ZX
Shi, ZZ
Fang, J
Gu, BW
Li, JM
Zhu, YM
Shi, JY
Zheng, PZ
Yan, H
Liu, YF
Chen, Y
Shen, Y
Wu, W
Tang, W
Waxman, S
de Thé, H
Wang, ZY
Chen, SJ
Chen, Z
机构
[1] Shanghai Med Univ 2, Shanghai Inst Hematol, Rui Jin Hosp, State Key Lab Med Genom, Shanghai 200025, Peoples R China
[2] Univ Paris 07, CNRS,Hop St Louis, Unite Propre Rech 9051, Lab Comite Paris Ligue Contre Canc, F-75475 Paris 10, France
[3] Mt Sinai Med Ctr, Dept Med, Div Neoplast Dis, New York, NY 10029 USA
关键词
D O I
10.1073/pnas.0400053101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Both all-trans retinoic acid (ATRA) and arsenic trioxide (As2O3) have proven to be very effective in obtaining high clinical complete remission (CR) rates in acute promyelocytic leukemia (APL), but they had not been used jointly in an integrated treatment protocol for remission induction or maintenance among newly diagnosed APL patients. In this study, 61 newly diagnosed APL subjects were randomized into three treatment groups, namely by ATRA, As2O3, and the combination of the two drugs. CR was determined by hematological analysis, tumor burden was examined with real-time quantitative RT-PCR of the PML-RARalpha (promyelocytic leukemia-retinoic acid receptor a) fusion transcripts, and side effects were evaluated by means of clinical examinations. Mechanisms possibly involved were also investigated with cellular and molecular biology methods. Although CR rates in three groups were all high (greater than or equal to90%), the time to achieve CR differed significantly, with that of the combination group being the shortest one. Earlier recovery of platelet count was also found in this group. The disease burden as reflected by fold change of PML-RARa transcripts at CR decreased more significantly in combined therapy as compared with ATRA or As2O3 mono-therapy (P < 0.01). This difference persisted after consolidation (P < 0.05). Importantly, all 20 cases in the combination group remained in CR whereas 7 of 37 cases treated with mono-therapy relapsed (P < 0.05) after a follow-up of 8-30 months (median: 18 months). Synergism of ATRA and As2O3 on apoptosis and degradation of PML-RARa oncoprotein might provide a plausible explanation for superior efficacy of combinative therapy in clinic. In conclusion, the ATRA/As2O3 combination for remission/maintenance therapy of APL brings much better results than either of the two drugs used alone in terms of the quality of CR and the status of the disease-free survival.
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收藏
页码:5328 / 5335
页数:8
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