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。
9 K$ r$ O4 L# \8 I5 ], @. \ 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。% k, [! z& T( f/ L6 c
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作者:来自澳大利亚
4 D% ~! C# B X3 `% c来源:Haematologica. 2011.8.9.
d+ q5 D- _- v; [. F( FDear Group,
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Some of you are on Dasatinib (Sprycel) and we wish to give news on all CML
2 x0 W. J2 I/ a) D. h5 `therapies. Here is a report from Australia on 3 patients who went off Sprycel7 s9 H. Q# P/ y- m
after stable molecular response (PCRU). 1 patient relapsed but 2/3 patients
: _9 V! ?& t& A0 [, Nremain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel
: w. ~, _1 ^5 l8 Cdoes spike up the immune system so I hope more reports come out on this issue.+ D9 q; b+ s2 y
: Z' |/ ^' P1 F7 L3 g5 x6 t8 N$ WThe remarkable news about Sprycel cessation is that all 3 patients had failed$ u; r# c- d9 P+ i
Gleevec and Sprycel was their second TKI so they had resistant disease. This is1 J1 v7 v! q: f6 T7 X
different from the stopping Gleevec trial in France which only targets patients
+ t0 y$ j% [% Y4 I1 Mwho have done well on Gleevec.
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( E0 u$ ~3 |- A* a5 g! M8 KHopefully, the doctors will report on a larger study and long-term to see if the
S- \% X2 L: v' w, d& ~response off Sprycel is sustained.$ {5 W+ Q7 E# l) ~0 c2 s: c
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Best Wishes,5 `& X" d/ q. A
Anjana# W8 d7 ~3 l9 ]2 O7 |4 \* w
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1 v7 q6 j8 y5 z) i" iHaematologica. 2011 Aug 9. [Epub ahead of print]" i( s- u" z0 c% O+ {
Durable complete molecular remission of chronic myeloid leukemia following' b5 R. }* m/ E& \1 H
dasatinib cessation, despite adverse disease features.
! X# g5 i0 J0 H$ ?- C# ]4 a: k: eRoss DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.
* M& \$ E% S. n i3 iSource
/ U; ~$ Y( n0 A2 d3 g- fAdelaide, Australia;3 o6 X, E4 j% L7 c0 y
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Abstract7 O- B) m4 [/ J% G7 i1 G6 `
Patients with chronic myeloid leukemia, treated with imatinib, who have a
7 e, |( @* J, edurable complete molecular response might remain in CMR after stopping
- Y6 L7 o( m2 m& T# G2 `% Ptreatment. Previous reports of patients stopping treatment in complete molecular
, e# I, i* Q. ?) l2 S# I: |0 Fresponse have included only patients with a good response to imatinib. We# ?) _* [8 k& t9 y( n
describe three patients with stable complete molecular response on dasatinib6 {% U# h" b E* M6 y3 D
treatment following imatinib failure. Two of the three patients remain in1 S1 O+ D( o4 t6 {
complete molecular response more than 12 months after stopping dasatinib. In$ [" ^; c& O3 C2 f% W% N
these two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to5 ]7 [- @) p( ~: {' x
show that the leukemic clone remains detectable, as we have previously shown in
( ~. l: k8 [* @% n/ Wimatinib-treated patients. Dasatinib-associated immunological phenomena, such as
' Z7 x$ x4 h4 ^2 g( x/ z& k/ @( ^the emergence of clonal T cell populations, were observed both in one patient5 ]- ~: y" E4 r2 ~ n+ J
who relapsed and in one patient in remission. Our results suggest that the, z# W& L2 G% K: D# l/ S
characteristics of complete molecular response on dasatinib treatment may be
7 J9 M- t) e; w$ P) |; z; Esimilar to that achieved with imatinib, at least in patients with adverse
0 n. }5 W3 G" k! ]- e4 p% Zdisease features.
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