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。
! V0 d+ {$ W& V1 I) R# L- m. K& P 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! d, h( G% |# t! l7 c K
来源:Haematologica. 2011.8.9., F/ L& |! _. V. Z+ _
Dear Group,
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Some of you are on Dasatinib (Sprycel) and we wish to give news on all CML0 U. r; X" c, R4 g# K
therapies. Here is a report from Australia on 3 patients who went off Sprycel
" ?, N) n! W7 e% Gafter stable molecular response (PCRU). 1 patient relapsed but 2/3 patients3 ~5 w0 s8 U' H; u& t( @# f0 G# C
remain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel
- V2 N5 \* |4 c! ddoes spike up the immune system so I hope more reports come out on this issue./ G# {; Q! Y5 f# q& o5 d
& ~# L* s' e, Z0 i; L' ^: JThe remarkable news about Sprycel cessation is that all 3 patients had failed
) ]: Y, S0 L3 C ^# D/ }Gleevec and Sprycel was their second TKI so they had resistant disease. This is2 ^) _: C W& n
different from the stopping Gleevec trial in France which only targets patients
* f( ^6 @2 ^8 H9 Nwho have done well on Gleevec.
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) N7 K# e) k- Z" D2 I! c* yHopefully, the doctors will report on a larger study and long-term to see if the4 Z3 x4 q) e8 y) T' J
response off Sprycel is sustained.+ K# ?0 i( d, w
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Best Wishes,4 A5 M: K8 I2 R) W: j* u5 u
Anjana% b9 ?, M; f1 b: o
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Haematologica. 2011 Aug 9. [Epub ahead of print]( C/ } A( l3 y; S7 i, p+ s0 Z
Durable complete molecular remission of chronic myeloid leukemia following( w0 Q: `" E8 R8 }( O# t' m
dasatinib cessation, despite adverse disease features.+ D" b" ^& O) v4 Y4 `* A2 g0 c
Ross DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.
! X* x$ K2 w$ qSource
' C( q; ]% x/ EAdelaide, Australia;1 A) s: ]: ~- M6 E) P* O3 k
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Abstract% B2 ^. A# e3 ]# c
Patients with chronic myeloid leukemia, treated with imatinib, who have a
$ s( R3 n$ T* B e0 wdurable complete molecular response might remain in CMR after stopping: o$ E' m/ M# _( P/ ?' ?
treatment. Previous reports of patients stopping treatment in complete molecular
3 h: M) h+ }+ {: e9 U lresponse have included only patients with a good response to imatinib. We
8 O& h/ b/ o2 U" ], y' ?describe three patients with stable complete molecular response on dasatinib# a' ^1 W8 q9 m" b$ n
treatment following imatinib failure. Two of the three patients remain in
1 y% u% J$ R2 j1 m* l* s. ncomplete molecular response more than 12 months after stopping dasatinib. In
3 p, u" C/ m/ a1 t- o4 a9 [these two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to8 Q6 c3 I4 f4 n6 C {1 u
show that the leukemic clone remains detectable, as we have previously shown in
6 i$ _2 D3 I( A* K- ]* E; i0 b$ Qimatinib-treated patients. Dasatinib-associated immunological phenomena, such as& \- a5 t5 ]- o, N
the emergence of clonal T cell populations, were observed both in one patient
0 m, w" l7 ?& Ewho relapsed and in one patient in remission. Our results suggest that the
- v& l0 L, k/ M/ a j! L& xcharacteristics of complete molecular response on dasatinib treatment may be, ^; h: |: \4 X! X$ O* P
similar to that achieved with imatinib, at least in patients with adverse
- w# Y6 M2 J! K: q _disease features.
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