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 A C: G9 Y, a! a4 |
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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作者:来自澳大利亚' E% v0 }8 B& k- y$ V s! ^
来源:Haematologica. 2011.8.9.( v' D# C& }+ m- Y4 d
Dear Group,
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0 ?! A' }+ ^; a2 [% G8 ASome of you are on Dasatinib (Sprycel) and we wish to give news on all CML
# Z& g( B- O9 u5 q" f! vtherapies. Here is a report from Australia on 3 patients who went off Sprycel8 h; G, M9 Q( i' V2 n4 | w
after stable molecular response (PCRU). 1 patient relapsed but 2/3 patients4 m6 ]. i: ~8 E) Q6 Y
remain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel
. E5 S& b) w( |8 F3 m% Y5 Qdoes spike up the immune system so I hope more reports come out on this issue.; v9 C5 J( g* C; K2 x1 k5 u3 P0 C6 k
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The remarkable news about Sprycel cessation is that all 3 patients had failed
& D. A' r3 |0 V% kGleevec and Sprycel was their second TKI so they had resistant disease. This is
9 X1 r6 Z L9 E8 o1 q* xdifferent from the stopping Gleevec trial in France which only targets patients
' V, _) o" J* q# U2 K5 j& b( rwho have done well on Gleevec.& r1 v1 Z O7 L3 |# h+ a3 x
# ]2 n, \; R, }8 X7 h3 l0 D0 ]" G( oHopefully, the doctors will report on a larger study and long-term to see if the H* D! [5 |9 M2 }4 j7 i/ M d! _
response off Sprycel is sustained. J0 E5 T# W5 L
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Best Wishes,
8 v. ^% Y. ^& ~8 IAnjana! j, d- {- @" ?! O4 n7 R: v
$ v1 W; i9 u2 k h. ?8 \; V+ L4 k8 W7 o! m. w0 r( E
* G6 ~+ i. i6 b4 [ J, THaematologica. 2011 Aug 9. [Epub ahead of print]2 h$ L& A8 N2 Y9 K2 ^( ^0 z
Durable complete molecular remission of chronic myeloid leukemia following) W" X9 G- a( x, f
dasatinib cessation, despite adverse disease features.
! U1 P( c i B# n( D5 z' ERoss DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.
) {/ ^3 i# s0 YSource; Y4 s8 Z) c; w% I
Adelaide, Australia;
* U: h# P! f# @' L: I! @8 |! Q$ v0 B
" e$ a: {2 O7 M. KAbstract
E6 p' ?% }" H+ x: f! R9 F# pPatients with chronic myeloid leukemia, treated with imatinib, who have a0 E1 s2 _; _* {+ u6 [6 |% y
durable complete molecular response might remain in CMR after stopping2 e( Y4 [: X, \7 S7 b' i. P# Z) @6 A
treatment. Previous reports of patients stopping treatment in complete molecular
# Y9 o! B6 J* X! x! wresponse have included only patients with a good response to imatinib. We
$ t9 S7 t T" Z2 z5 O8 r2 Bdescribe three patients with stable complete molecular response on dasatinib
$ I: t+ F' R. y* Utreatment following imatinib failure. Two of the three patients remain in
4 {' h1 m! s8 l5 x. bcomplete molecular response more than 12 months after stopping dasatinib. In/ N9 {) j: ^4 f: k' K
these two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to
& E0 d. j' M8 d$ F9 E! d6 eshow that the leukemic clone remains detectable, as we have previously shown in
: I3 @2 r0 u, B) {; Mimatinib-treated patients. Dasatinib-associated immunological phenomena, such as
! s" R: ]3 K7 L+ H$ \( Hthe emergence of clonal T cell populations, were observed both in one patient
2 C2 p3 ]* o; t8 j) o; qwho relapsed and in one patient in remission. Our results suggest that the+ M; T8 a1 U3 o5 C H
characteristics of complete molecular response on dasatinib treatment may be! W) U( a2 }+ t$ @. X& D( o
similar to that achieved with imatinib, at least in patients with adverse
4 v0 Y: V- B8 U* X6 Zdisease features.: J @1 f9 [' Z- H+ v
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