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。, u0 J+ j+ M }) X" j8 d
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
' M( f N5 E6 l; w来源:Haematologica. 2011.8.9.
0 j( j& _* P) f2 ?7 Y4 M6 A: cDear Group,
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. p0 @1 N' T: A- r5 cSome of you are on Dasatinib (Sprycel) and we wish to give news on all CML
. { x+ Q$ \+ V2 ?$ Q0 I% btherapies. Here is a report from Australia on 3 patients who went off Sprycel# C7 D1 w, S; S9 i1 \; o' u
after stable molecular response (PCRU). 1 patient relapsed but 2/3 patients
/ Q) C, j4 P+ {0 Y* Y/ qremain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel
0 R# r% l" a5 o* L( E. qdoes spike up the immune system so I hope more reports come out on this issue.4 g. S M6 p7 ?* T
$ u( L; l0 f# ]7 h4 |The remarkable news about Sprycel cessation is that all 3 patients had failed
( T* J8 |) d% j+ j7 xGleevec and Sprycel was their second TKI so they had resistant disease. This is, h$ \/ v1 s9 R# g$ l
different from the stopping Gleevec trial in France which only targets patients3 W8 ~3 W! V* E* h q! o( m
who have done well on Gleevec.1 t: w+ B( e% G0 x
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Hopefully, the doctors will report on a larger study and long-term to see if the5 g6 I* K' N& ]# u, g8 N
response off Sprycel is sustained.
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7 k, o5 `' A" m- PBest Wishes,
8 h) B, V5 g+ [ m8 L( z9 ^. h3 v" tAnjana
2 T+ ] T7 {6 K# v7 P* G# o8 c, f( w5 V
0 i f+ Q$ P; j! T
/ C% M& g6 B6 |3 hHaematologica. 2011 Aug 9. [Epub ahead of print]4 Q0 v: t$ H( |" Y2 `
Durable complete molecular remission of chronic myeloid leukemia following
4 V' r" p# ~. v; l s3 z5 zdasatinib cessation, despite adverse disease features.( g3 |$ F1 Y% M' k
Ross DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.
/ i; \% H- v; S( j8 [Source
* Q" P9 n2 E& L2 B9 EAdelaide, Australia;
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Abstract) f5 n ~% j3 s1 V& N
Patients with chronic myeloid leukemia, treated with imatinib, who have a4 E* z; y8 X+ N& f$ {! y
durable complete molecular response might remain in CMR after stopping
a3 O% A$ D" ?- R! B' ^treatment. Previous reports of patients stopping treatment in complete molecular
, c0 h$ t, `5 l6 mresponse have included only patients with a good response to imatinib. We& {* C& Q3 \ E( Z
describe three patients with stable complete molecular response on dasatinib
1 ^) v; ? y& z) Atreatment following imatinib failure. Two of the three patients remain in* G* \4 G j8 T' f" B% C( }+ J
complete molecular response more than 12 months after stopping dasatinib. In) [- _) C( V8 Z
these two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to
9 J. Z2 F% Z/ j1 m* G, Bshow that the leukemic clone remains detectable, as we have previously shown in0 h0 K0 w6 u- ~3 a7 J6 f+ A
imatinib-treated patients. Dasatinib-associated immunological phenomena, such as
4 A# ^5 J( h$ Y& ?8 |the emergence of clonal T cell populations, were observed both in one patient
{8 w L7 v" q1 k3 |1 Vwho relapsed and in one patient in remission. Our results suggest that the
9 J. _7 q$ i6 B3 {9 s3 Rcharacteristics of complete molecular response on dasatinib treatment may be7 @* f w2 z! O4 j: k0 V2 [% {" }
similar to that achieved with imatinib, at least in patients with adverse
1 X, o' V/ G. u2 Z: f e/ R; _disease features.3 k. L6 L$ Y) M6 {+ w; x7 y% f/ {
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