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。, ?7 S7 T; Q* x3 k5 ?- H' o
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。" r; Q/ ]/ Y t h. I% `
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作者:来自澳大利亚
% X- p6 n0 r# Y1 k: }5 x来源:Haematologica. 2011.8.9.+ D$ ], \: L+ e, {3 h
Dear Group,
6 `; J! g& M9 i4 B# J. b+ S7 o4 N5 X
- X2 C* z Z3 d+ ]4 LSome of you are on Dasatinib (Sprycel) and we wish to give news on all CML; `, s/ S7 Z( x! E$ s
therapies. Here is a report from Australia on 3 patients who went off Sprycel
3 F" H8 ^* R$ B, R% Fafter stable molecular response (PCRU). 1 patient relapsed but 2/3 patients
" E. F6 V& b' I. Dremain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel
" w% p% q) N& ?/ O' Kdoes spike up the immune system so I hope more reports come out on this issue.
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) x" a0 T" w6 Z( l3 |The remarkable news about Sprycel cessation is that all 3 patients had failed4 e+ q+ s+ L' ^' h8 g' V
Gleevec and Sprycel was their second TKI so they had resistant disease. This is9 t: g" E0 o" K+ E
different from the stopping Gleevec trial in France which only targets patients
4 c! a2 U1 [& j3 swho have done well on Gleevec.
3 }0 E% s/ h4 W) u8 }2 d0 f( Q: }6 A$ x+ b- H" i( I' P6 K
Hopefully, the doctors will report on a larger study and long-term to see if the
3 f5 P4 G9 J( Wresponse off Sprycel is sustained.
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Best Wishes,
' H4 i( N3 k, WAnjana1 M `! v7 r' {
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' ^) T* O! D# |3 J. k! w' VHaematologica. 2011 Aug 9. [Epub ahead of print]
3 l4 L: A" i) Z# i; _: Y- nDurable complete molecular remission of chronic myeloid leukemia following' b0 B& ]/ n c; T$ y. @+ b
dasatinib cessation, despite adverse disease features.6 s4 y) x* a, \
Ross DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.
9 S" c* C$ v- s% Q6 e0 ^% z& A: KSource
* f0 h) `5 t& Y! }- D0 R; tAdelaide, Australia;' q/ _5 n; g; F3 r
: X4 p+ ]* g% k+ [
Abstract2 ]% {( i2 i. _- t0 V
Patients with chronic myeloid leukemia, treated with imatinib, who have a: O, q H4 S1 I% @6 Z' ~
durable complete molecular response might remain in CMR after stopping2 Y1 l3 S9 O; Q8 P0 |) ? L
treatment. Previous reports of patients stopping treatment in complete molecular
. }- j* Q9 r: U) y/ r* lresponse have included only patients with a good response to imatinib. We& `: w1 P0 c, ~2 B P( t; ~
describe three patients with stable complete molecular response on dasatinib" k* H2 c j/ K
treatment following imatinib failure. Two of the three patients remain in
- S5 m! ]% M% J. o1 f ocomplete molecular response more than 12 months after stopping dasatinib. In
q3 X& O$ i& F4 m& Qthese two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to
8 c' I+ B8 K- ashow that the leukemic clone remains detectable, as we have previously shown in5 A, ^3 z: P1 t- ?
imatinib-treated patients. Dasatinib-associated immunological phenomena, such as& _6 K" e6 _9 i, W; \9 v F& _
the emergence of clonal T cell populations, were observed both in one patient; m5 K. k& o1 q8 A3 i$ g2 }3 x% K
who relapsed and in one patient in remission. Our results suggest that the
1 [+ t$ h! V' d2 s: Z1 |& q& s& ncharacteristics of complete molecular response on dasatinib treatment may be
+ o6 _7 P: Y6 P! o" Usimilar to that achieved with imatinib, at least in patients with adverse2 s2 R: V3 I! R
disease features.( {1 y& V, Q% e* Z- q
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