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。6 |: c* n$ e1 I# C8 G. D# {
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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! _' O4 j/ U1 x) f+ R& ]作者:来自澳大利亚
( E* {2 F& f9 a8 Q% x( X! Q- B来源:Haematologica. 2011.8.9.0 S7 z$ c$ L& r8 z E, x
Dear Group,. O. u% ~+ ~# m
) U7 W6 J; N6 b3 oSome of you are on Dasatinib (Sprycel) and we wish to give news on all CML
0 m9 ~; a$ i$ x& jtherapies. Here is a report from Australia on 3 patients who went off Sprycel
, G/ `0 a6 y4 F6 S0 Bafter stable molecular response (PCRU). 1 patient relapsed but 2/3 patients4 M9 |5 {" B/ B- a# m
remain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel( D" `& M( _" C( p% x3 t
does spike up the immune system so I hope more reports come out on this issue.& O4 V+ Y C1 o8 _0 [" F I- ?- t6 C7 h; L
( j- w! k$ k: p* lThe remarkable news about Sprycel cessation is that all 3 patients had failed/ \9 [! _: l: P* O. c5 W! x' k. ~9 U
Gleevec and Sprycel was their second TKI so they had resistant disease. This is' ]/ @& P X1 J. i9 m ?, a
different from the stopping Gleevec trial in France which only targets patients
# N. s7 q* E7 B0 w+ |who have done well on Gleevec.4 Q$ o. `; R& v, @! ?( h
& O$ J2 U! \4 lHopefully, the doctors will report on a larger study and long-term to see if the* @ r' O! O; n# R4 _; ]
response off Sprycel is sustained.6 p/ W, ?5 F$ @
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Best Wishes,& j. B0 ]0 e% u+ d
Anjana
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$ Y% q a5 d/ d3 \; mHaematologica. 2011 Aug 9. [Epub ahead of print]
& I. R! {- z5 ?4 a! r0 n. NDurable complete molecular remission of chronic myeloid leukemia following& o, o H' h' d6 ]: \4 N5 y: t
dasatinib cessation, despite adverse disease features.
0 }( Y0 W# d9 `2 x. J7 S3 fRoss DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.4 c5 s7 R. {4 I$ E; p- h9 _
Source/ C" C$ n5 z1 j! k2 y; U
Adelaide, Australia;% R2 ]8 H5 Y- B% g) x0 `* R
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Abstract
5 I4 D) A# a. T1 \" F) }( \; uPatients with chronic myeloid leukemia, treated with imatinib, who have a$ Q( {$ }* D# N- A9 F
durable complete molecular response might remain in CMR after stopping
# ~, S) c8 K" W8 I* ltreatment. Previous reports of patients stopping treatment in complete molecular( ^! v, Y; N$ }, g& v
response have included only patients with a good response to imatinib. We" ^$ S, `% S& v7 S2 U
describe three patients with stable complete molecular response on dasatinib6 y9 T* x8 X+ f; ~5 G) Z9 C, B
treatment following imatinib failure. Two of the three patients remain in: `- E' A0 r6 j
complete molecular response more than 12 months after stopping dasatinib. In/ j( \7 ~" A! R: I2 t; E
these two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to
5 V* ?6 [5 I. Eshow that the leukemic clone remains detectable, as we have previously shown in
5 k$ [! o% g; y6 X& fimatinib-treated patients. Dasatinib-associated immunological phenomena, such as
7 O: a: R# r$ A: C6 x" l2 c3 k9 Vthe emergence of clonal T cell populations, were observed both in one patient
! V1 w7 F0 a+ Q5 Fwho relapsed and in one patient in remission. Our results suggest that the! o5 {; f0 ~; ^0 d
characteristics of complete molecular response on dasatinib treatment may be0 e; S* x3 Y1 Z9 h; _
similar to that achieved with imatinib, at least in patients with adverse
; r" S; G& Z- A6 K( zdisease features.
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