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。7 `; ?* p0 b8 ?6 X* j, V
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 m* P" D7 \9 r$ H O
2 u+ }. a" _+ o) Z作者:来自澳大利亚: @6 t( I0 w" G5 |5 Z0 d
来源:Haematologica. 2011.8.9./ x* c, D1 u7 ]7 A5 J* ~
Dear Group,) s6 Z9 @; B7 S" w
: H* t) {% W/ m* j) Q& s7 Z& u# uSome of you are on Dasatinib (Sprycel) and we wish to give news on all CML
8 {( w3 {" _( T: [therapies. Here is a report from Australia on 3 patients who went off Sprycel
: C: `: b' K9 Q# ?7 [after stable molecular response (PCRU). 1 patient relapsed but 2/3 patients; T8 Y/ L* K g7 o, G
remain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel
& ^: ~: T* Q' _- f* _# g1 _does spike up the immune system so I hope more reports come out on this issue.
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" S! u% `. {+ i1 p" k. tThe remarkable news about Sprycel cessation is that all 3 patients had failed8 p" {1 E; F! ?+ h8 Q( E7 X
Gleevec and Sprycel was their second TKI so they had resistant disease. This is! x2 U& B. i! C
different from the stopping Gleevec trial in France which only targets patients- k% Y5 |5 o# P; w7 N( z- M/ s" f
who have done well on Gleevec.* Y; g7 S: l, A+ F1 D
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Hopefully, the doctors will report on a larger study and long-term to see if the
# H; P+ l* W( G$ m! ]response off Sprycel is sustained.
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Best Wishes, ]) v! R/ N5 f* H& e& q% Y
Anjana* s& P! |, S4 b6 d" W* J
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Haematologica. 2011 Aug 9. [Epub ahead of print]
2 I9 P9 O# f% |* J; w# [Durable complete molecular remission of chronic myeloid leukemia following# x V* F- e4 r+ g' t5 {: J$ q0 E
dasatinib cessation, despite adverse disease features.# S* }- s3 a. L1 H9 q$ g. ~. w! M! ?
Ross DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP. S# _! ~( I; U9 i. w: ]
Source
& O7 L7 Q# i g2 h! k( r: LAdelaide, Australia;
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Abstract/ H! _8 B/ w+ w1 L9 _0 @3 w3 w, }& v4 o
Patients with chronic myeloid leukemia, treated with imatinib, who have a
2 d5 w6 d8 ]7 M1 n8 h6 Kdurable complete molecular response might remain in CMR after stopping
, K& c! \! D' |% Btreatment. Previous reports of patients stopping treatment in complete molecular7 W" t5 S5 ?1 K3 b% [! y
response have included only patients with a good response to imatinib. We' W- l @" ]7 G
describe three patients with stable complete molecular response on dasatinib6 l3 ]5 L) q3 K( n, u
treatment following imatinib failure. Two of the three patients remain in; K. I7 i3 W6 \! g1 f3 X
complete molecular response more than 12 months after stopping dasatinib. In
5 g, @9 v" v C8 K9 Y- \& fthese two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to' w6 L& H3 C7 w0 @7 u$ v5 C* `
show that the leukemic clone remains detectable, as we have previously shown in0 h$ `$ e: ^. H @
imatinib-treated patients. Dasatinib-associated immunological phenomena, such as* ^1 y3 d, l& g. J$ \1 C
the emergence of clonal T cell populations, were observed both in one patient' L$ i% Z& T! N8 g% S- x) S- N7 ^
who relapsed and in one patient in remission. Our results suggest that the
6 c! Q$ i- x2 o7 H0 `characteristics of complete molecular response on dasatinib treatment may be
O# n% Y( y! q* z! I/ psimilar to that achieved with imatinib, at least in patients with adverse
4 ]- I3 ^: h0 L; sdisease features.
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