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。
' s! N# Q8 D0 S9 V8 {* p 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。
% x; V0 `2 V( b9 H
; R$ o6 K7 B4 K作者:来自澳大利亚
0 ~! [ k9 h: I0 b1 ]2 b) o来源:Haematologica. 2011.8.9.
5 s+ l4 i' X4 I0 G8 a1 }Dear Group,
6 J8 V6 N* Z1 N) E! a: g+ n$ D: c) Z/ |( A5 L+ P6 X
Some of you are on Dasatinib (Sprycel) and we wish to give news on all CML& t/ ] \2 V4 O
therapies. Here is a report from Australia on 3 patients who went off Sprycel
+ d, T0 O' t& L) {1 d8 kafter stable molecular response (PCRU). 1 patient relapsed but 2/3 patients0 j2 T& z( c. `6 p1 |! v
remain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel
- E- j! v1 l9 K' U9 K9 Ldoes spike up the immune system so I hope more reports come out on this issue.
& ~' W" V) {; V. I" q
2 F1 E% g2 _6 X$ |( X6 [The remarkable news about Sprycel cessation is that all 3 patients had failed; \2 U4 ~7 ^* c" ~
Gleevec and Sprycel was their second TKI so they had resistant disease. This is
, o9 M2 [$ g7 l A. hdifferent from the stopping Gleevec trial in France which only targets patients; a8 F) W6 y5 m3 [, Y1 D& @/ `2 `
who have done well on Gleevec.
* _4 g. c+ Y# X4 { K2 ^9 M0 ?
# L( V3 ?, N$ c/ v: Z, YHopefully, the doctors will report on a larger study and long-term to see if the6 J/ a( I& W5 @
response off Sprycel is sustained.
3 g+ r9 \5 D2 U5 ], T) s- C! g# R# m4 h0 i$ W5 }. R
Best Wishes,
. m7 H8 y3 V. ^( X. G. F3 ZAnjana
* M, `" A) {# `# [# ~
: H6 h2 f! ^; M" k2 I6 I+ }4 h5 |, I+ Y5 I8 B L
d) w$ n% P8 z" [! E" f4 RHaematologica. 2011 Aug 9. [Epub ahead of print]7 ^: ~$ D6 `( F
Durable complete molecular remission of chronic myeloid leukemia following
; h/ w' ?4 L o. adasatinib cessation, despite adverse disease features.+ R+ z6 F$ R9 P& x0 v
Ross DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.
; Y( z" x" o1 I/ jSource9 O9 r5 ^1 Q. I! h% G4 p7 }
Adelaide, Australia;; D' ^* q, X2 G# o9 {1 V" {
% i3 d6 m2 Y/ q9 \1 P- ]
Abstract
+ O1 d7 M+ K* b1 [ t: A; HPatients with chronic myeloid leukemia, treated with imatinib, who have a( A& _( N, l% M. [7 S% d6 ^2 }1 }
durable complete molecular response might remain in CMR after stopping
- y5 g! p, G6 x4 A/ ^treatment. Previous reports of patients stopping treatment in complete molecular
9 B, l; H' _( v, i6 Zresponse have included only patients with a good response to imatinib. We
; x9 l9 z' t8 q1 E& Jdescribe three patients with stable complete molecular response on dasatinib
( u. Q: V8 d* A" x' xtreatment following imatinib failure. Two of the three patients remain in
' C& e& J4 H9 j) B5 Wcomplete molecular response more than 12 months after stopping dasatinib. In
' }/ s& y1 Y# U# m1 Wthese two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to/ V, |4 Z4 @7 s
show that the leukemic clone remains detectable, as we have previously shown in$ S, l1 k& N% Q8 N U
imatinib-treated patients. Dasatinib-associated immunological phenomena, such as ] ]! u% t- l7 V J3 g* k7 Y
the emergence of clonal T cell populations, were observed both in one patient/ B6 g; l4 U3 C* d1 |3 |. z
who relapsed and in one patient in remission. Our results suggest that the6 I4 p! h" c: C9 a h1 J2 R6 s" Z* g
characteristics of complete molecular response on dasatinib treatment may be
9 }2 o& ^# o0 _9 ?$ O2 i0 Psimilar to that achieved with imatinib, at least in patients with adverse+ q Q9 ^) Y/ O7 N& }& w. X
disease features.+ l; v& P5 F* u
|