摘要:这3名患者在取得稳定的分子学缓解之后(融合基因转阴PCRU)停用达沙替尼。1名患者复发,另外两名患者在1年后仍保持了PCRU。以前说过,达沙替尼确实可以提高免疫力,希望今后能获得更多的相关研究报告。; I' X3 x$ F: y! _
关于这个研究值得注意的是,这三名患者都是服用格列卫失败后转用达沙替尼的,也即他们对格列卫是耐药的。这与法国的格列卫停药研究又有所不同,那个研究中的患者都是对格列卫反应良好的。希望医生们能扩大研究长期观察,看看停用达沙替尼是否能持久不复发。
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作者:来自澳大利亚! Y: X7 i4 v( z6 L; j" D" @8 W
来源:Haematologica. 2011.8.9.4 X1 S6 R0 E! s0 T/ e: b
Dear Group,: v5 U4 N8 O$ _8 F4 L( q
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Some of you are on Dasatinib (Sprycel) and we wish to give news on all CML
. Q/ E% b2 N/ |1 g. S* I- |7 T3 Htherapies. Here is a report from Australia on 3 patients who went off Sprycel
( h Z# |( e2 h8 q7 Jafter stable molecular response (PCRU). 1 patient relapsed but 2/3 patients
! j/ c* S2 R' C. v8 C1 I# u6 Y Xremain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel5 I0 |% s0 F2 D' K
does spike up the immune system so I hope more reports come out on this issue. j, z5 w% G2 o$ H
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The remarkable news about Sprycel cessation is that all 3 patients had failed5 p. n3 ?2 _$ x
Gleevec and Sprycel was their second TKI so they had resistant disease. This is
; q1 B" D. f* ^( Jdifferent from the stopping Gleevec trial in France which only targets patients) _) s6 b0 V3 l- e) b
who have done well on Gleevec.* ?0 h* U+ Y1 B" Y" A0 z& ]! M
# X) V% I6 o" S$ A k; o5 uHopefully, the doctors will report on a larger study and long-term to see if the! Z& z1 Q+ C, q% h$ J; T
response off Sprycel is sustained.- x) A* y$ N3 S1 A
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Best Wishes,
5 w. k" ^/ E; S% WAnjana, ?4 T$ L1 ]& ~# u' C2 ]# x; }
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Haematologica. 2011 Aug 9. [Epub ahead of print]# v2 v" }( j: v+ V8 [2 V
Durable complete molecular remission of chronic myeloid leukemia following/ ]+ Z3 p4 g1 ^* t
dasatinib cessation, despite adverse disease features.
4 ?! V. }$ j+ [. @Ross DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.
3 E3 w; q4 \$ i3 q. _- ASource
: g; d7 T! X$ l }& i5 eAdelaide, Australia;5 b, f* x1 X; y) ^
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Abstract& T: h0 ~$ b/ V; V
Patients with chronic myeloid leukemia, treated with imatinib, who have a
8 M* ^0 g% _0 R! k: ~* l) {3 _durable complete molecular response might remain in CMR after stopping: P8 B+ ?" s' A/ D( H/ k3 s( h4 b
treatment. Previous reports of patients stopping treatment in complete molecular
P( l) o7 F3 _: v/ J% b4 ^6 Kresponse have included only patients with a good response to imatinib. We
$ h4 @% f. | `! v- w5 O5 Kdescribe three patients with stable complete molecular response on dasatinib. r) N+ `: E7 Z2 E' `
treatment following imatinib failure. Two of the three patients remain in4 G* _ b: X! E! c! d
complete molecular response more than 12 months after stopping dasatinib. In
6 g+ v! f4 J8 X5 Ythese two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to. F. x2 W3 W2 C+ Z) K2 w1 Q
show that the leukemic clone remains detectable, as we have previously shown in9 r! n$ v* C8 a( A5 C- x
imatinib-treated patients. Dasatinib-associated immunological phenomena, such as" }. v2 x5 n6 y* s! E) p' O
the emergence of clonal T cell populations, were observed both in one patient
5 N2 Q: M; v8 d% {3 D6 Q4 Ywho relapsed and in one patient in remission. Our results suggest that the* ]; t# s9 w8 }1 H
characteristics of complete molecular response on dasatinib treatment may be d6 f6 c& R, S8 |8 R' R" R# m3 x
similar to that achieved with imatinib, at least in patients with adverse
1 i& Y% @7 f& c+ ^0 s2 O. g% Udisease features.: S% T5 l. A( e8 P5 H
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