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。+ u2 R8 x9 a( r
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5 C9 F& I1 w! L; c6 _8 D
来源:Haematologica. 2011.8.9.) ^3 e1 m! Y' }' L
Dear Group,4 G) Q* N4 G" |+ q q t# Q5 z
}2 R. l4 e% T1 [: x5 j% Q) nSome of you are on Dasatinib (Sprycel) and we wish to give news on all CML# n1 a' w$ {! g' W6 `
therapies. Here is a report from Australia on 3 patients who went off Sprycel. |8 L+ P9 A- b4 T: k: X
after stable molecular response (PCRU). 1 patient relapsed but 2/3 patients( G" _( Y: M8 C' Y
remain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel; D6 {( q. G: c6 f( U, C: [
does spike up the immune system so I hope more reports come out on this issue.
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% s4 Z5 C3 i7 E8 v \9 n: ~The remarkable news about Sprycel cessation is that all 3 patients had failed
4 D2 M% O7 z3 N/ d v5 x& oGleevec and Sprycel was their second TKI so they had resistant disease. This is
3 K6 U0 T( R! e; H& [. Vdifferent from the stopping Gleevec trial in France which only targets patients
6 L. i8 `1 g2 ^! e6 R% fwho have done well on Gleevec.4 D9 c$ d* D N. {' P$ e5 Q
( l* Q+ ~1 P$ f+ Q( g. sHopefully, the doctors will report on a larger study and long-term to see if the
% U- \' P: o5 w- ~2 O3 Bresponse off Sprycel is sustained. i8 i% T$ Z: v6 {
; e% A1 Y6 D9 ^* L" c- I3 aBest Wishes," g# {: u' ~. z( ^; r
Anjana
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9 I8 @# E' H. K% X5 J" S6 D" T2 c/ W7 {# n% q" J" m# q) e7 }7 U
Haematologica. 2011 Aug 9. [Epub ahead of print]& i" c. P8 V/ f! q- O" c$ W
Durable complete molecular remission of chronic myeloid leukemia following
! @! x8 J4 h! R' L- Bdasatinib cessation, despite adverse disease features.0 ]! b8 q% T9 p* d4 }; m
Ross DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.5 N& n- w1 N9 j" o
Source
" N7 Z2 v( j8 L8 T& P: QAdelaide, Australia;+ y0 `/ a/ C8 A" i8 r L
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Abstract% y! M9 l- K+ K. {4 G+ F' J6 g
Patients with chronic myeloid leukemia, treated with imatinib, who have a
5 H: I* p3 ?$ @( K( _- }, jdurable complete molecular response might remain in CMR after stopping
: G% u9 x' B! e( d: C- itreatment. Previous reports of patients stopping treatment in complete molecular5 O6 e1 \+ V7 B: i- D g, T
response have included only patients with a good response to imatinib. We- o- h* i( |5 s! b+ r
describe three patients with stable complete molecular response on dasatinib
0 z6 j* u8 l& Q: z$ c- Gtreatment following imatinib failure. Two of the three patients remain in
6 w6 @: J }. t. o: e+ m& ccomplete molecular response more than 12 months after stopping dasatinib. In' h5 P U0 S' K
these two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to
( I7 E) k0 U1 s$ b& r" }show that the leukemic clone remains detectable, as we have previously shown in; `0 U% l5 x8 r+ C. `, k1 d
imatinib-treated patients. Dasatinib-associated immunological phenomena, such as
' A5 U4 j6 q9 ]5 f+ E" n W3 Nthe emergence of clonal T cell populations, were observed both in one patient
; h. R5 y* [. _8 lwho relapsed and in one patient in remission. Our results suggest that the
4 R( ]1 y& K& k0 d1 G: p5 a1 y5 {- Hcharacteristics of complete molecular response on dasatinib treatment may be. ?: ^) j0 q9 G+ t8 R
similar to that achieved with imatinib, at least in patients with adverse" J, H% X5 C j
disease features.3 ~/ F/ i. O- ]7 _4 q9 ?
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