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。
- H; F2 }5 V# t. a0 b# T2 [ 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。- \' b: Q8 { ^ P- J/ D2 W0 A
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作者:来自澳大利亚
' d( N3 |# C8 Y+ Y来源:Haematologica. 2011.8.9.' ~( X- F, I1 k @& c0 O
Dear Group,+ l# e$ ^ m# p. Q2 E
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Some of you are on Dasatinib (Sprycel) and we wish to give news on all CML' b y+ @+ ^& d! ?
therapies. Here is a report from Australia on 3 patients who went off Sprycel; X" R. c9 v* k* N# q/ C% ]# B
after stable molecular response (PCRU). 1 patient relapsed but 2/3 patients6 m7 B% [8 F; O5 M
remain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel4 F( j+ q6 [! u5 \) C* q
does spike up the immune system so I hope more reports come out on this issue.' E( P! G ?5 z5 ?3 N
. {4 |* L5 \% Y0 n+ g/ l. tThe remarkable news about Sprycel cessation is that all 3 patients had failed
/ r( B1 o" m) ^Gleevec and Sprycel was their second TKI so they had resistant disease. This is
# x6 p0 n7 z+ c, l6 q/ p5 Rdifferent from the stopping Gleevec trial in France which only targets patients+ \" Q$ g# w) Y1 @0 F. \
who have done well on Gleevec.
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Hopefully, the doctors will report on a larger study and long-term to see if the/ B, I/ j5 i4 E: y ~
response off Sprycel is sustained.
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- |: v+ g3 B2 p" ~) K* ~& ?& HBest Wishes,7 z3 q& j. f G
Anjana! r* N q; v* q" E1 b. T7 l
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Haematologica. 2011 Aug 9. [Epub ahead of print]- x: x7 j. M% G( f) d5 g0 T
Durable complete molecular remission of chronic myeloid leukemia following
4 E2 Z3 z$ Z8 h+ B, fdasatinib cessation, despite adverse disease features.( e0 [6 N3 i- p; F. x% w
Ross DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.( w) B7 ?: d% d* i$ e0 \
Source
`! C/ v8 W" O: U9 v! jAdelaide, Australia;+ q( b, b% N+ g& D9 J
& Y d$ K% g3 ]9 l* e: N, `Abstract6 m5 x9 R! R2 b: d5 |
Patients with chronic myeloid leukemia, treated with imatinib, who have a. {3 |6 l6 f7 u/ y, ?
durable complete molecular response might remain in CMR after stopping
/ Z& B# Y2 O( a h5 @treatment. Previous reports of patients stopping treatment in complete molecular( K7 x+ B% J( t* `
response have included only patients with a good response to imatinib. We( @% v# A$ J- F4 K# s9 d; r
describe three patients with stable complete molecular response on dasatinib
$ @, @( Y& m+ \# a* {4 m% _treatment following imatinib failure. Two of the three patients remain in- N# O" @5 Q: Y7 N2 P* @/ ], B
complete molecular response more than 12 months after stopping dasatinib. In6 t8 K) f/ m5 m, g3 c
these two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to9 e- l# ^% z3 v4 m0 e$ W
show that the leukemic clone remains detectable, as we have previously shown in. }5 m" J9 ~+ T# X5 i
imatinib-treated patients. Dasatinib-associated immunological phenomena, such as9 a) u3 ?7 c- o8 p/ T
the emergence of clonal T cell populations, were observed both in one patient
0 w# u: {1 @/ z! D8 ]! z! qwho relapsed and in one patient in remission. Our results suggest that the5 P! Z' q) m$ A+ L
characteristics of complete molecular response on dasatinib treatment may be
& r) C1 V% v5 g% h+ g Y" w Dsimilar to that achieved with imatinib, at least in patients with adverse5 ?/ Y, e7 c4 c0 ]: D5 I
disease features.
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