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。! M8 x% A& c) r1 S& q4 g 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。( ~; Z- v/ ]: Q+ ]! e" B! z
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作者:来自澳大利亚; b# i! u; V4 F
来源:Haematologica. 2011.8.9.
2 g2 m8 o g0 m; k2 X0 dDear Group,0 G8 ?, e- m7 @$ x2 z7 p
$ b* l" h' Z* W. o! oSome of you are on Dasatinib (Sprycel) and we wish to give news on all CML
* V3 H9 C1 w% W% _0 ]' ltherapies. Here is a report from Australia on 3 patients who went off Sprycel% @. u4 y4 P% P8 l4 l9 M: v
after stable molecular response (PCRU). 1 patient relapsed but 2/3 patients
1 W1 ?& S% x5 kremain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel3 q( P" L2 T. n0 t. R' o
does spike up the immune system so I hope more reports come out on this issue.. C0 ~/ T# U i% V8 e+ e# L
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The remarkable news about Sprycel cessation is that all 3 patients had failed
3 U4 e& |% a) g3 C; f( DGleevec and Sprycel was their second TKI so they had resistant disease. This is1 r% W; X/ p0 y+ _. [% U, p6 T
different from the stopping Gleevec trial in France which only targets patients
- R1 ^, \0 C, T" J. F# ?. H2 owho have done well on Gleevec.
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Hopefully, the doctors will report on a larger study and long-term to see if the
; d' D# `: X- ~response off Sprycel is sustained.; l) x) k5 K/ ]- f/ j
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Best Wishes,5 n3 C2 a! r! @1 ?0 J0 y! ~7 \
Anjana
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- l* G1 m+ C; t/ ^Haematologica. 2011 Aug 9. [Epub ahead of print]6 r1 L% w U- c" D0 W( C4 H
Durable complete molecular remission of chronic myeloid leukemia following; O' C" @% R7 r+ t; A0 y' T& D
dasatinib cessation, despite adverse disease features.
% `0 Y8 v, S' h2 S9 PRoss DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.: `7 v' _9 e) P' V$ U
Source
C$ f% }; U0 C: ]0 h1 lAdelaide, Australia;
: C+ {6 @' P7 _! e; J: ?; ~1 K0 m: J: n- X
Abstract W% T Y+ s1 d3 m7 i; {" ~% k
Patients with chronic myeloid leukemia, treated with imatinib, who have a' z- Q8 r3 c( v' N( H! A
durable complete molecular response might remain in CMR after stopping) Z( b# z! A" C) a1 T9 Y
treatment. Previous reports of patients stopping treatment in complete molecular
& }; H, u2 ]5 V7 B8 t: f) A; d+ tresponse have included only patients with a good response to imatinib. We" G/ `/ x; N. G
describe three patients with stable complete molecular response on dasatinib$ V8 h3 H$ n' ~% d/ f' @; E# z6 q
treatment following imatinib failure. Two of the three patients remain in
5 c7 \0 ^* [4 c- F" lcomplete molecular response more than 12 months after stopping dasatinib. In
5 x/ D4 w. [: Z6 `these two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to& N0 w- R: i) r8 s% [
show that the leukemic clone remains detectable, as we have previously shown in' V6 g4 R8 D: `2 O
imatinib-treated patients. Dasatinib-associated immunological phenomena, such as
1 w5 O# \; q) i4 _: a+ \4 Fthe emergence of clonal T cell populations, were observed both in one patient
6 s3 e" W8 l- [. s5 mwho relapsed and in one patient in remission. Our results suggest that the
$ i+ F' s( a6 p1 Fcharacteristics of complete molecular response on dasatinib treatment may be
N; i$ K, I5 Bsimilar to that achieved with imatinib, at least in patients with adverse) `& i6 v. V A( ^1 J: F) Q
disease features.
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