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。
" e, }; Y* R% G: b5 H* S0 p9 q 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。, _5 E. T1 r0 c$ F# u2 h
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作者:来自澳大利亚" w' L5 @ ^9 F' ~9 K; q
来源:Haematologica. 2011.8.9.8 N1 R7 P/ i: A! |# R9 b
Dear Group,; z ^5 h; t9 I" ^9 U* k
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Some of you are on Dasatinib (Sprycel) and we wish to give news on all CML) i! z+ F$ l* R5 }& u/ T4 U
therapies. Here is a report from Australia on 3 patients who went off Sprycel
0 V, t" X9 w+ x/ D4 v: safter stable molecular response (PCRU). 1 patient relapsed but 2/3 patients
3 b4 A4 g& p! F( C. t7 [remain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel
& {* N+ `% E. rdoes spike up the immune system so I hope more reports come out on this issue.1 B$ e6 _0 Q& V: p1 S9 I" v
1 a: f; I; M, H u6 x7 R( C
The remarkable news about Sprycel cessation is that all 3 patients had failed/ s n8 @* h$ ~. c' B4 ~
Gleevec and Sprycel was their second TKI so they had resistant disease. This is$ z% f n" l0 F$ }
different from the stopping Gleevec trial in France which only targets patients1 O+ o \% Q$ n- ?& ~2 D
who have done well on Gleevec.0 b2 S: I5 p/ s6 `0 D
" F; g9 b9 ^3 S. I1 U. xHopefully, the doctors will report on a larger study and long-term to see if the/ D1 a$ G2 _8 x6 y; i
response off Sprycel is sustained.
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3 a* p0 _% J h- w, K7 a6 I- iBest Wishes,
! E ]0 W- D* TAnjana5 y# x U. h# l
* L; I4 ^: y. e4 w+ X5 o* Q5 c5 a7 h
* i: C( o( ?9 BHaematologica. 2011 Aug 9. [Epub ahead of print]
4 Y. }' V0 W f: H- NDurable complete molecular remission of chronic myeloid leukemia following% E& E* i) I+ E f
dasatinib cessation, despite adverse disease features.
. g- k a; ]# @- I5 mRoss DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP." u8 ]9 u c% {4 G1 m- H6 J0 U0 x
Source
1 D2 k; U3 n7 V JAdelaide, Australia;
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Abstract; D+ o0 ^ e# H8 c# G1 p6 y) ~
Patients with chronic myeloid leukemia, treated with imatinib, who have a4 l5 h3 e6 C l% M
durable complete molecular response might remain in CMR after stopping
6 l; y# a- [0 ~) [" E& vtreatment. Previous reports of patients stopping treatment in complete molecular
0 E3 E# d7 W4 p: Z( Presponse have included only patients with a good response to imatinib. We( F7 m8 y. S" E
describe three patients with stable complete molecular response on dasatinib8 h: [9 B1 O* S1 H: T
treatment following imatinib failure. Two of the three patients remain in
- X/ k# d9 a- n& zcomplete molecular response more than 12 months after stopping dasatinib. In
2 p# h& ~1 Y1 g. o# P. \( e4 {these two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to# b, @" k; m8 @
show that the leukemic clone remains detectable, as we have previously shown in) {( @1 R* v7 \ b
imatinib-treated patients. Dasatinib-associated immunological phenomena, such as
$ b6 ^& J5 Q# q/ kthe emergence of clonal T cell populations, were observed both in one patient
8 a5 z- ]5 s+ V; R1 o* D8 [1 g$ Y: kwho relapsed and in one patient in remission. Our results suggest that the* O8 L6 \- C, w3 u. u9 h! L$ ~1 l
characteristics of complete molecular response on dasatinib treatment may be4 ]$ R5 v7 W; t; A. [+ m
similar to that achieved with imatinib, at least in patients with adverse( w! i2 {2 K# E( g6 h) y O) X
disease features.$ V& ?5 j2 O) c3 ?! f
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