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。
8 _0 _5 G, P8 ^1 X# P6 q% n: `! 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。: H; j: Q) j `+ p% O. Q
- K) T) S) @" O( }' N; @+ @0 ^0 U
作者:来自澳大利亚
N1 ]2 |' p1 n e. i g来源:Haematologica. 2011.8.9." v6 P/ c% h e. s; X
Dear Group,/ Z5 u* m8 j: g- O$ ?7 N
' r9 [( Y/ v7 c! V! hSome of you are on Dasatinib (Sprycel) and we wish to give news on all CML9 B: ]2 U" G$ Y% C& E# |2 n
therapies. Here is a report from Australia on 3 patients who went off Sprycel
& ?# w) J2 {3 P2 ~* g9 B7 H' J$ w/ {after stable molecular response (PCRU). 1 patient relapsed but 2/3 patients* n: J8 @; E+ z2 [. |9 ]- q
remain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel
3 v# M$ V0 f7 `: ^( wdoes spike up the immune system so I hope more reports come out on this issue.
# `* ~6 w# m6 g( |7 w, `
7 M0 B G3 }, i, ?, TThe remarkable news about Sprycel cessation is that all 3 patients had failed
' F& v' U& O8 _0 q C' |6 S* X' wGleevec and Sprycel was their second TKI so they had resistant disease. This is
N+ d6 K( L( C e" Z F0 tdifferent from the stopping Gleevec trial in France which only targets patients+ H$ ?* I- j2 ]6 ^
who have done well on Gleevec.8 B. d; P6 Y! m7 [
; w3 R( M( { @ eHopefully, the doctors will report on a larger study and long-term to see if the. n% w& b8 k6 E4 P( u" q+ n: W
response off Sprycel is sustained.3 l$ p+ A5 w9 Q# T7 C3 g
5 Y8 @! j3 |/ i' ^$ Z5 oBest Wishes,. D. M9 l$ w# l- L4 G, w! x
Anjana! w7 I8 b+ _( [
2 [ _3 l+ @8 {5 T! u
1 ?# p" E- `2 z; Q* C* @# Z ?7 a% \& S% X# g# H: O1 K
Haematologica. 2011 Aug 9. [Epub ahead of print]" r! p% g7 s. u1 s
Durable complete molecular remission of chronic myeloid leukemia following+ S9 I3 c0 |5 G |! }; k1 C
dasatinib cessation, despite adverse disease features.
* ~7 m1 W# B: q; fRoss DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.
' x3 J6 V0 S( c" D% WSource% \$ P8 v: W0 l! |5 }$ {
Adelaide, Australia;( _$ t. @- |+ p% z! p
! w6 _* k! S3 b+ E) e
Abstract: Z! h+ K* V* Z' |# J! s# u- s
Patients with chronic myeloid leukemia, treated with imatinib, who have a' ~5 t7 j7 S/ {- @8 B) u( J: ?' _; g
durable complete molecular response might remain in CMR after stopping
' F+ ?+ j- | A! W; ~& M' Ttreatment. Previous reports of patients stopping treatment in complete molecular
9 n7 `4 H9 c' z9 Q8 dresponse have included only patients with a good response to imatinib. We& ~/ M# h g; h- ~3 S5 e) x2 Y
describe three patients with stable complete molecular response on dasatinib8 G! L5 `. K. E1 T& e8 t; e
treatment following imatinib failure. Two of the three patients remain in
" ]( Z j7 Z3 }0 M% ecomplete molecular response more than 12 months after stopping dasatinib. In
, G& p4 B! g" m' O* Z) T, \* Rthese two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to
1 {4 e& M2 J. I$ g! I7 f' E9 `show that the leukemic clone remains detectable, as we have previously shown in) n7 Z8 T; D* b
imatinib-treated patients. Dasatinib-associated immunological phenomena, such as
/ t4 _" C. h0 g( u# {" p! `the emergence of clonal T cell populations, were observed both in one patient
$ n' }- e' F2 d$ }: V. zwho relapsed and in one patient in remission. Our results suggest that the8 \/ _9 t0 G+ r- z( y5 W
characteristics of complete molecular response on dasatinib treatment may be W$ P2 J' T A* a: F0 l G
similar to that achieved with imatinib, at least in patients with adverse: F+ q- k4 K4 B% P. q
disease features.
! Q! E7 }' d7 q2 L |