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。* p' `% K" t: {) m$ _: M* r/ V% 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。- w2 R8 i8 a" \# ~! T
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作者:来自澳大利亚1 C( u: P, p; O6 A( S
来源:Haematologica. 2011.8.9.
' ^! P' i) s$ s8 u' jDear Group,- o" q& B z" [% e, x
2 h9 j c# l. a. d" MSome of you are on Dasatinib (Sprycel) and we wish to give news on all CML2 p W4 x3 K2 J
therapies. Here is a report from Australia on 3 patients who went off Sprycel
" A+ u0 {" L" a" b7 wafter stable molecular response (PCRU). 1 patient relapsed but 2/3 patients
4 L' D5 l' r. c- b8 ~+ n8 |1 Lremain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel
+ W: b8 F) C2 z/ h* Zdoes spike up the immune system so I hope more reports come out on this issue.
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O% u( I- S% \0 QThe remarkable news about Sprycel cessation is that all 3 patients had failed
# J3 V' ~" A) i- gGleevec and Sprycel was their second TKI so they had resistant disease. This is
! H' U! [( W3 Z9 Fdifferent from the stopping Gleevec trial in France which only targets patients4 J/ ?6 |" _0 c+ m+ N& R; u% w+ H- u4 K
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
$ R9 P4 Z8 P$ Rresponse off Sprycel is sustained.
' i J% X9 h! |1 T S& |4 _! \
Best Wishes, l G4 l7 g3 w: g( }
Anjana
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) K4 A' j0 W) {' p& y; f: RHaematologica. 2011 Aug 9. [Epub ahead of print]
: \' |0 M Q% r, NDurable complete molecular remission of chronic myeloid leukemia following5 b3 m6 x' J: G
dasatinib cessation, despite adverse disease features.) \* |- ~" H0 B. x+ m, b
Ross DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.
+ ~# V4 N" h+ F, S: b# R! r9 u7 |Source: I, m- k K' m" E# K. |. s
Adelaide, Australia;
: J8 V! b/ E' U& U/ y# m3 q# O* h) G6 O8 J7 d$ e+ o1 L) [
Abstract
' I9 C8 a5 h# \9 R7 gPatients with chronic myeloid leukemia, treated with imatinib, who have a6 f2 p7 r3 x0 D- G4 L4 k8 q# J
durable complete molecular response might remain in CMR after stopping- l: U* S6 t" k$ W
treatment. Previous reports of patients stopping treatment in complete molecular# q0 }1 D+ @- @3 R: [
response have included only patients with a good response to imatinib. We Z( d' M4 S" e5 C d# d0 X
describe three patients with stable complete molecular response on dasatinib
9 r/ u' A! t9 ]/ Gtreatment following imatinib failure. Two of the three patients remain in2 O" T8 n% F* a; {: R+ g
complete molecular response more than 12 months after stopping dasatinib. In" i) [9 t# w k+ Z& f9 K# g
these two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to' a2 U3 L/ U) e5 T% B: s
show that the leukemic clone remains detectable, as we have previously shown in
t9 L$ W7 [# Kimatinib-treated patients. Dasatinib-associated immunological phenomena, such as
% u' s: ~9 _& y" {. j# D5 Q9 \the emergence of clonal T cell populations, were observed both in one patient
; o4 _% ~7 ^; E6 ~! q; D# \who relapsed and in one patient in remission. Our results suggest that the
: v) x0 B; P8 m. U. acharacteristics of complete molecular response on dasatinib treatment may be
4 D# B& L( Z. ?" |) Asimilar to that achieved with imatinib, at least in patients with adverse
9 ?+ U: ? O; j2 [" q) x+ [4 cdisease features.6 q7 d: s0 [5 X; Z4 p: o; F, p
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