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。& l( B6 w9 T3 \' z5 o4 z& s
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。" p/ [ B3 x& m. e9 A' t
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作者:来自澳大利亚
" B P* H; X f) P9 j来源:Haematologica. 2011.8.9.
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Some of you are on Dasatinib (Sprycel) and we wish to give news on all CML; r2 [7 B2 L( t
therapies. Here is a report from Australia on 3 patients who went off Sprycel. x2 X e" j: V* l# N$ R+ Q
after stable molecular response (PCRU). 1 patient relapsed but 2/3 patients- `' p3 R" X* m4 a5 y0 ]$ Y
remain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel: q8 v1 N5 d0 j, H- L% }- q
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
$ B) i2 S. S) A3 \# q: HGleevec and Sprycel was their second TKI so they had resistant disease. This is
6 ]9 r1 ~9 G% d5 Hdifferent from the stopping Gleevec trial in France which only targets patients
3 B- Z; A: m. a( V1 {/ @. swho have done well on Gleevec.+ d* ]$ G0 P* C2 i- b$ w
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Hopefully, the doctors will report on a larger study and long-term to see if the6 I- ?, M+ Y9 {0 t% \8 H `
response off Sprycel is sustained.4 W/ |6 |1 Q7 Y' G
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Best Wishes,
' z/ V, K) T$ |% W5 e4 ~Anjana
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Haematologica. 2011 Aug 9. [Epub ahead of print]+ }4 J; C) S" s: `0 K/ U* P
Durable complete molecular remission of chronic myeloid leukemia following
1 _* \9 U8 U3 q+ w+ p% edasatinib cessation, despite adverse disease features.
' N3 Y( f6 B$ w1 KRoss DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.9 o0 [ R! `& c
Source
* C0 t/ |8 b2 X8 |4 z# lAdelaide, Australia;
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Abstract$ U0 a1 [2 }7 u' |
Patients with chronic myeloid leukemia, treated with imatinib, who have a
2 N2 P. _& p$ Kdurable complete molecular response might remain in CMR after stopping/ p3 p2 d4 t9 w% C
treatment. Previous reports of patients stopping treatment in complete molecular! {8 A: o% [% \3 ~% l1 Q
response have included only patients with a good response to imatinib. We3 r- ]; Q$ h% i) N1 r6 }, ~/ ?
describe three patients with stable complete molecular response on dasatinib" M6 h6 P; L8 }7 g7 s8 `3 b
treatment following imatinib failure. Two of the three patients remain in
. p3 |) H" s0 M" f' fcomplete molecular response more than 12 months after stopping dasatinib. In
% I- U% Y' z$ @! mthese two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to( g. n1 q* t; B$ g2 I( u6 e- L! m
show that the leukemic clone remains detectable, as we have previously shown in' ^ M, t+ T& U/ Q( ~* q' F
imatinib-treated patients. Dasatinib-associated immunological phenomena, such as# r! F% ^0 A" [ O# `' Y3 @
the emergence of clonal T cell populations, were observed both in one patient" w# v/ G9 h1 k4 A9 q
who relapsed and in one patient in remission. Our results suggest that the, `1 ]$ ?- V! [. l
characteristics of complete molecular response on dasatinib treatment may be4 Z, C+ I, b, N! P/ ~
similar to that achieved with imatinib, at least in patients with adverse8 p- {: x2 ~# h* z' _$ s1 g
disease features.$ a) f" f3 ~- ?: b! j: y, S: ~
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