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。; ?! d: J! U# |% B# ^( e! g
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
1 N0 W8 o5 L- A; o* }% J9 W$ T2 a$ p. d2 M来源:Haematologica. 2011.8.9.
5 y; Q* D7 b; d" YDear Group,' L k9 w5 b. P: X( u' ]
B4 \( P N5 Y! n7 J* \& QSome of you are on Dasatinib (Sprycel) and we wish to give news on all CML9 e! A4 c; |5 B. S( e" L6 m6 g
therapies. Here is a report from Australia on 3 patients who went off Sprycel3 p6 f: |4 D% \# M
after stable molecular response (PCRU). 1 patient relapsed but 2/3 patients
* C& }9 e# C I; Nremain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel
& U8 f" K* c Qdoes spike up the immune system so I hope more reports come out on this issue.
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9 P, {- e5 {1 U# ^+ w8 UThe remarkable news about Sprycel cessation is that all 3 patients had failed
8 G1 q- k0 J+ ]& \+ v) w( p) iGleevec and Sprycel was their second TKI so they had resistant disease. This is
* e: }; P! P' S. r- Ddifferent from the stopping Gleevec trial in France which only targets patients
! i, _9 x$ u" f7 e0 O: U. Cwho have done well on Gleevec.' Z9 h, q" i1 {# E e" D
3 l* @! k- C0 ?' EHopefully, the doctors will report on a larger study and long-term to see if the
) a' q3 k* O, H) Tresponse off Sprycel is sustained.
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1 T9 T( Y% F8 [ I! u3 ABest Wishes,
* M& _" f* s. D1 L' B# W8 U6 t. P% x! `' ]Anjana
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Haematologica. 2011 Aug 9. [Epub ahead of print]3 }& v8 G X7 t: Y; h& s
Durable complete molecular remission of chronic myeloid leukemia following
/ B" M; \& v i- S. M* c% Ddasatinib cessation, despite adverse disease features.
1 I# t* U0 D6 L9 r% SRoss DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.+ x' P" e |1 p p
Source1 w5 T! ~- E, j. X1 C" }+ ?
Adelaide, Australia;- ?& i: ~6 T9 S0 s2 _
$ k! q6 h' ^' eAbstract
9 b, _/ }, g+ i s% P( wPatients with chronic myeloid leukemia, treated with imatinib, who have a
4 S" b1 `/ ?/ ~, hdurable complete molecular response might remain in CMR after stopping2 _# k# X4 V4 u9 Q; S7 c7 }( ~- }" ?
treatment. Previous reports of patients stopping treatment in complete molecular
4 A% z5 G; J& D1 Q4 mresponse have included only patients with a good response to imatinib. We1 e! q& U4 z$ o; H
describe three patients with stable complete molecular response on dasatinib
/ Q! w/ g0 _% z' [treatment following imatinib failure. Two of the three patients remain in
: G5 p7 P: Z4 n8 L4 K6 |complete molecular response more than 12 months after stopping dasatinib. In' _- E4 t+ {/ p
these two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to
7 H4 w9 w$ G0 R4 a ~show that the leukemic clone remains detectable, as we have previously shown in
5 C& v# B. C8 T1 Fimatinib-treated patients. Dasatinib-associated immunological phenomena, such as
5 c4 W5 x' J% Y; w" r' y& _/ qthe emergence of clonal T cell populations, were observed both in one patient' ?4 @: R; k+ M# e6 l# `
who relapsed and in one patient in remission. Our results suggest that the' K7 ~7 k( g) T' e
characteristics of complete molecular response on dasatinib treatment may be
* Z/ j. H4 [# R) Lsimilar to that achieved with imatinib, at least in patients with adverse
8 r4 X# y" t8 h3 G. b0 Wdisease features.( g7 m& o q% Y$ j' [9 A
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