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。
; M$ f: V% c( F# 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。
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& j. B/ `; m, m! [9 Z作者:来自澳大利亚- v! k2 a$ ?9 k3 B' B: Q7 V1 P- v
来源:Haematologica. 2011.8.9.# A" [- H9 `% k* V
Dear Group,7 _) h' f( W0 `7 K
' b/ `2 Y$ A8 r! SSome of you are on Dasatinib (Sprycel) and we wish to give news on all CML" u- }4 T9 i; K$ g) [- I8 A& e
therapies. Here is a report from Australia on 3 patients who went off Sprycel9 z S- H% k3 M- A
after stable molecular response (PCRU). 1 patient relapsed but 2/3 patients
& T, @# F$ Y$ e6 H( Cremain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel4 n( s. Y- {* w4 o$ c8 _. c
does spike up the immune system so I hope more reports come out on this issue.( J* g( ]2 m- u% Y' t. q1 w
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The remarkable news about Sprycel cessation is that all 3 patients had failed
: s% A$ c* [' [+ m2 cGleevec and Sprycel was their second TKI so they had resistant disease. This is
* m1 a* p0 P6 }# G/ @5 |different from the stopping Gleevec trial in France which only targets patients
7 Y" _) z7 h" t& |6 Awho have done well on Gleevec.9 n1 a3 q* M. D# U
. \% Q5 C% D ^, e- I" QHopefully, the doctors will report on a larger study and long-term to see if the- B; \. ~/ l7 L8 O
response off Sprycel is sustained.
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Best Wishes,% g1 w# }' }" w7 f
Anjana
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- f( A3 Q: m. N+ o% t! H: M- _2 [' {4 I. v+ v/ e: y G
Haematologica. 2011 Aug 9. [Epub ahead of print]
% `, K2 N: n4 ^ f( iDurable complete molecular remission of chronic myeloid leukemia following( J/ L1 M" o- I
dasatinib cessation, despite adverse disease features.
% R8 R2 s% h# i8 k" U$ P# S/ URoss DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.
: R. H1 ~; {" s6 ~6 L8 K: o9 lSource
7 L. K+ v5 U( EAdelaide, Australia;2 p7 x1 j+ J, ~8 m# B9 o
5 o1 H% i5 ]! Y- j1 JAbstract4 ^0 x5 g3 S1 g
Patients with chronic myeloid leukemia, treated with imatinib, who have a* ~( u/ t r7 _9 W0 ~$ ~" l
durable complete molecular response might remain in CMR after stopping [, s# E1 \. ^" f& J; ^% h. K2 _0 `
treatment. Previous reports of patients stopping treatment in complete molecular
# k8 N7 K6 r/ g+ T6 i% i2 @1 y: a8 zresponse have included only patients with a good response to imatinib. We5 h! K i2 `/ ~+ c" ~% y0 B
describe three patients with stable complete molecular response on dasatinib
8 h( m1 O$ o6 k: k8 r s+ O6 w7 }treatment following imatinib failure. Two of the three patients remain in
% ^8 H0 n ^! s4 U; v: [complete molecular response more than 12 months after stopping dasatinib. In$ t6 ~3 _: w* b3 g% a
these two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to: y2 K6 h5 c( Q1 `' r
show that the leukemic clone remains detectable, as we have previously shown in
4 ]# D0 r( k& A0 j' @1 A) ?imatinib-treated patients. Dasatinib-associated immunological phenomena, such as) d$ g: k9 J' ]. j
the emergence of clonal T cell populations, were observed both in one patient
, }: o$ h; k% m# T! T! ewho relapsed and in one patient in remission. Our results suggest that the
. k# Y) ~8 O4 |( M" ?- V0 e/ jcharacteristics of complete molecular response on dasatinib treatment may be+ S7 ~1 R; Q$ h: x: m; @8 ?
similar to that achieved with imatinib, at least in patients with adverse
; W% D: a4 ~3 N/ Ndisease features.' m. ^( [2 X' {* Q2 n: A1 W
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