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。
# _- ?% _% c: ?7 A% b+ o' I0 G% v 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。4 x0 _" ~) w, W/ A- M
0 s( c- [5 o9 b9 p" c( X作者:来自澳大利亚( i1 v3 I& O. O, G3 _5 z3 t
来源:Haematologica. 2011.8.9.
4 ?$ j' J' l9 p* U/ Q: O3 J; S$ zDear Group,0 ?9 {* A: M) V; N& L) `
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Some of you are on Dasatinib (Sprycel) and we wish to give news on all CML0 V) B: N# S3 w( D1 m! M
therapies. Here is a report from Australia on 3 patients who went off Sprycel
, _# t# W' x. Q- M- {$ Aafter stable molecular response (PCRU). 1 patient relapsed but 2/3 patients$ Z5 @! u0 \) e# a
remain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel
6 s1 X0 i q& I& n$ C1 R% [does spike up the immune system so I hope more reports come out on this issue. `, o# v5 {2 i6 i1 L
) o( Q2 B- G! c/ Y2 T ]5 oThe remarkable news about Sprycel cessation is that all 3 patients had failed
Y3 \8 z0 B" \1 BGleevec and Sprycel was their second TKI so they had resistant disease. This is
1 `( X+ g0 E7 x3 I* tdifferent from the stopping Gleevec trial in France which only targets patients1 H% r/ N% j0 E1 [' c3 \. }+ @# E7 v
who have done well on Gleevec.+ G& h- n* T2 z& O+ ^1 R* X$ E2 J
* D# B( d7 N- RHopefully, the doctors will report on a larger study and long-term to see if the! j2 | m1 @. m( X* ^
response off Sprycel is sustained., }% {* y. i3 [( O. t& h
" P( {7 O$ P! q' R" @& |: JBest Wishes,: K7 k- B5 F" S
Anjana
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1 x5 b8 C% \' D/ y; B& XHaematologica. 2011 Aug 9. [Epub ahead of print]5 c' u: f. A' E: N l( m$ Y
Durable complete molecular remission of chronic myeloid leukemia following
) V7 |8 g8 T! H7 O) L& g, Q% Bdasatinib cessation, despite adverse disease features.* Q/ p& N, q& }- d$ T7 V, y4 r% o N
Ross DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.
9 n2 B; ]; U' f: `6 P. P9 _; KSource% }0 U; g% k) j. ?: k' P
Adelaide, Australia;
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1 m9 u3 g p5 V5 A. ?' \Abstract
$ a1 I9 n0 i& f* T" v* W+ E/ ?Patients with chronic myeloid leukemia, treated with imatinib, who have a/ B# G$ B3 @- p8 B
durable complete molecular response might remain in CMR after stopping
6 ^2 o) R9 e a* O) Q$ ptreatment. Previous reports of patients stopping treatment in complete molecular
, ?! |: d) g# g- {response have included only patients with a good response to imatinib. We
8 u( [" O& f- G1 u( [2 Cdescribe three patients with stable complete molecular response on dasatinib
5 T- [2 O. L# _treatment following imatinib failure. Two of the three patients remain in9 b$ [3 Q8 p. D. k6 s# S
complete molecular response more than 12 months after stopping dasatinib. In
5 Z; ^9 y" w" Jthese two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to- \7 n! g% t* H6 I
show that the leukemic clone remains detectable, as we have previously shown in
+ _2 p' T) ]8 W$ i; [. t9 Y' Oimatinib-treated patients. Dasatinib-associated immunological phenomena, such as& U9 S: b% ]: n+ D# a$ u% O9 \# x
the emergence of clonal T cell populations, were observed both in one patient
' M; z) k0 k k, X( q+ Xwho relapsed and in one patient in remission. Our results suggest that the5 @' \, ?2 L/ M& J% ~
characteristics of complete molecular response on dasatinib treatment may be3 } ?# P/ _$ \! F( n; Q
similar to that achieved with imatinib, at least in patients with adverse
; `. p1 g5 J2 M% P& q# ~! Udisease features.
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