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。
; E/ t$ `( y5 q/ G& W j+ L 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。! ^/ N H7 s! L& s/ W% D
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作者:来自澳大利亚# q; ]9 y9 ^, Q% k8 F$ X
来源:Haematologica. 2011.8.9.8 Q1 s; v$ x% ?5 @! Y6 l. X
Dear Group,
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Some of you are on Dasatinib (Sprycel) and we wish to give news on all CML6 `2 f5 b: @8 `& A! r- \
therapies. Here is a report from Australia on 3 patients who went off Sprycel
/ L/ G8 a+ e+ |( Lafter stable molecular response (PCRU). 1 patient relapsed but 2/3 patients' v. o1 S* U0 G6 }3 C
remain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel4 S- |; K. Q7 ~! _& N! u
does spike up the immune system so I hope more reports come out on this issue.
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The remarkable news about Sprycel cessation is that all 3 patients had failed. p2 b: Q8 R; e
Gleevec and Sprycel was their second TKI so they had resistant disease. This is
" i- f" d/ D% K2 m, k' \. `different from the stopping Gleevec trial in France which only targets patients9 I/ ?3 ?* a% e! d+ z
who have done well on Gleevec.5 r8 z- N. X, `5 F- N
' @- }3 `2 i1 sHopefully, the doctors will report on a larger study and long-term to see if the D* b1 Z- {% }, c! e
response off Sprycel is sustained.
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* `1 O8 l( t, t, sBest Wishes,4 [3 A6 Q5 s* Q; I# T( S
Anjana' a% x3 _ G& W4 f6 o6 D, Q
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8 i& h: w, e# N& k- dHaematologica. 2011 Aug 9. [Epub ahead of print]& t5 s& p" v$ k+ v- l5 E
Durable complete molecular remission of chronic myeloid leukemia following
- q+ B1 X& z- wdasatinib cessation, despite adverse disease features.( Y, o- u* {7 P
Ross DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP., }7 o2 H+ ]; R& |% u6 z% c
Source. K" T! B& P) \. N! Y
Adelaide, Australia;
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% C$ N" `& o$ o V8 W+ }Abstract
7 l) F) a3 [4 P( }+ L6 _" s& E6 U" L2 JPatients with chronic myeloid leukemia, treated with imatinib, who have a: L: M; l( e$ k5 v* A
durable complete molecular response might remain in CMR after stopping& _& H/ g1 K# l2 H" T+ }' U
treatment. Previous reports of patients stopping treatment in complete molecular
, [2 r- _ D6 h( W6 |! `2 _* {response have included only patients with a good response to imatinib. We
- f) c; Y" G# e9 sdescribe three patients with stable complete molecular response on dasatinib
2 W; ~# m5 l- h+ t* A, k4 x, utreatment following imatinib failure. Two of the three patients remain in
7 w* u. s( x3 L9 a0 Dcomplete molecular response more than 12 months after stopping dasatinib. In
$ v) u' {1 u& s0 X- Ethese two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to
* j% T9 C2 o( P2 R i; h9 hshow that the leukemic clone remains detectable, as we have previously shown in9 y6 o+ A1 B9 n5 P/ R: c" X
imatinib-treated patients. Dasatinib-associated immunological phenomena, such as
- P% A+ a+ X% S, _the emergence of clonal T cell populations, were observed both in one patient
4 x: X( |" I) d& c6 W5 mwho relapsed and in one patient in remission. Our results suggest that the; P; F' V1 i# S3 F( l3 e0 w; ~+ F* ?
characteristics of complete molecular response on dasatinib treatment may be
9 B! o4 ?2 G# J8 w: Jsimilar to that achieved with imatinib, at least in patients with adverse0 b6 O$ {1 E6 ~9 W
disease features.6 ]; E& G, ?4 j6 C3 A: D: ]7 Z2 G
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