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。9 \" T- m' ~5 D: d5 G* f3 @
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。# m3 q/ J4 k3 d
# d9 l2 p* s; W; w) Y; c4 ?% b作者:来自澳大利亚
: |+ i8 c2 ?: ^. {8 _, r4 |来源:Haematologica. 2011.8.9.
. [# j$ f; a) ?3 LDear Group,$ q: L% w. v, K- L9 k/ ?. V* [
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Some of you are on Dasatinib (Sprycel) and we wish to give news on all CML
( T8 J" A/ g9 u- J+ F* jtherapies. Here is a report from Australia on 3 patients who went off Sprycel- g3 m' M! r/ t1 J1 z2 A" V& R
after stable molecular response (PCRU). 1 patient relapsed but 2/3 patients
, v0 q/ R5 ~' g- b9 n' `, ~3 fremain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel
3 y i" P9 _7 w8 c2 q [& \3 zdoes spike up the immune system so I hope more reports come out on this issue.0 v; h- _/ q8 a2 M/ r4 ~' k. s
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The remarkable news about Sprycel cessation is that all 3 patients had failed% P7 k9 i- k; V l% V) X {
Gleevec and Sprycel was their second TKI so they had resistant disease. This is# ]0 D- I; ~7 R" e8 w
different from the stopping Gleevec trial in France which only targets patients0 z6 s1 e0 F: s
who 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
4 r3 V+ O) M4 v7 Q/ N- r6 Y& x4 kresponse off Sprycel is sustained.$ i6 M) s, ^1 E) ~/ m3 Y
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Best Wishes,
/ d, y* F; ?( n4 SAnjana
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7 q' y b. w+ d* L/ xHaematologica. 2011 Aug 9. [Epub ahead of print]. j! ]( k% E3 U5 V+ [
Durable complete molecular remission of chronic myeloid leukemia following8 w- L: Q8 ]5 F/ {
dasatinib cessation, despite adverse disease features.
0 r' q x& `4 _' ?2 V, s% k) dRoss DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.
3 g: G' F" Y6 _8 {/ @Source
) j( `* `- \; aAdelaide, Australia;5 H# F+ T6 b$ ^/ B) P3 o
* d \3 t) S2 L2 t* RAbstract0 W) z+ \4 b m( w3 C$ F# c
Patients with chronic myeloid leukemia, treated with imatinib, who have a
: c V( O; Q4 T: g* J5 K" ?durable complete molecular response might remain in CMR after stopping O9 X6 N( {5 Y0 `
treatment. Previous reports of patients stopping treatment in complete molecular; H, {2 _3 c$ ~, c5 t y; Q
response have included only patients with a good response to imatinib. We" }' p- ~* l/ X! n" B
describe three patients with stable complete molecular response on dasatinib
7 I; Y, X# j6 t6 W! W7 s p2 ytreatment following imatinib failure. Two of the three patients remain in' }4 y5 V( w6 b5 q* x( ^
complete molecular response more than 12 months after stopping dasatinib. In
* U5 f- c0 R) n- e: z' b8 V$ Othese two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to
/ j; R: ~7 M! Kshow that the leukemic clone remains detectable, as we have previously shown in
9 b/ W% L0 r3 X) h4 J% @! o& Cimatinib-treated patients. Dasatinib-associated immunological phenomena, such as" Z) f; Y( F3 Z# `$ N+ p
the emergence of clonal T cell populations, were observed both in one patient6 h0 a% ^( y; v. X
who relapsed and in one patient in remission. Our results suggest that the$ @! N: Z7 Z* _ i
characteristics of complete molecular response on dasatinib treatment may be
# S( U" ^, ]& Y$ H# m% Y. Y5 csimilar to that achieved with imatinib, at least in patients with adverse5 Y. f; c2 e; b! o$ d0 ?
disease features.5 f1 q$ B; A9 o; }" L/ I
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