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。9 O9 x: h0 x5 A+ ~# I
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。. B5 P% f, [- P: r/ S
0 ^. S6 [* B3 A" C3 L1 ^
作者:来自澳大利亚& e) v& L9 p" s) M
来源:Haematologica. 2011.8.9.
" s; J! q6 I5 _8 \Dear Group,' Y& Z. ?1 n7 ~# U. N
" _1 L. D1 Z% ySome of you are on Dasatinib (Sprycel) and we wish to give news on all CML ?$ z7 k( O9 q3 N0 t' y
therapies. Here is a report from Australia on 3 patients who went off Sprycel
+ P" U: s- l) N) O: A/ Bafter stable molecular response (PCRU). 1 patient relapsed but 2/3 patients+ Z. r8 p- i9 S4 T
remain in stable PCRU at the 1 year mark. Some of you may remember that Sprycel
: B$ Y2 V% j$ w2 z: wdoes spike up the immune system so I hope more reports come out on this issue.
& [+ _2 G' Z" _* x5 }( {/ ^7 t2 b3 H- G5 K, W8 @7 j
The remarkable news about Sprycel cessation is that all 3 patients had failed9 x0 V: x& S) F" Z
Gleevec and Sprycel was their second TKI so they had resistant disease. This is
0 H V, p4 U2 u) {9 [( ?different from the stopping Gleevec trial in France which only targets patients7 [$ u$ c$ c% L$ g; e3 _
who have done well on Gleevec.
2 r, f" w# s* s! \8 U
) h: o( q! {: U3 dHopefully, the doctors will report on a larger study and long-term to see if the' f: g9 |: Z; l
response off Sprycel is sustained.( ]0 a' i- H0 Z
5 C. R1 A, c+ a7 \8 U* H
Best Wishes,4 ]! }, U$ k# A
Anjana
8 j7 r& W6 B% g' s0 c* c
9 v+ h% y4 F! @6 h+ V. p- m8 {. u; t8 h* q! B0 G7 t+ k, q
6 X$ H: q- p1 V& K
Haematologica. 2011 Aug 9. [Epub ahead of print]; C' d# A9 e b# V1 G O2 W
Durable complete molecular remission of chronic myeloid leukemia following; j* i8 l7 Z o* }4 k& d/ ~" R5 x
dasatinib cessation, despite adverse disease features.- X" `0 I8 }7 d* t
Ross DM, Bartley PA, Goyne J, Morley AA, Seymour JF, Grigg AP.
& c9 \; I" n" ~6 x1 `Source
; \6 E% K& n% y) x, W" g1 E7 MAdelaide, Australia;4 ~8 ?) b4 a; v# w+ ]2 P* K
|; y6 a5 L7 G* z/ Y8 gAbstract
( t) n+ g1 i. APatients with chronic myeloid leukemia, treated with imatinib, who have a3 G8 S2 b& e+ D, r
durable complete molecular response might remain in CMR after stopping
- d C" G) w& Y9 Y/ M j( |treatment. Previous reports of patients stopping treatment in complete molecular9 L8 _, ^; P: i
response have included only patients with a good response to imatinib. We
# j. W3 X- f) cdescribe three patients with stable complete molecular response on dasatinib
' w% ^ s8 a: N/ s% y7 E3 [treatment following imatinib failure. Two of the three patients remain in
8 z. q. Q8 e5 [' ?" m ]+ kcomplete molecular response more than 12 months after stopping dasatinib. In
4 o2 O1 a0 J* T- G/ fthese two patients we used highly sensitive patient-specific BCR-ABL1 DNA PCR to } |7 Y8 {+ m+ Y2 Z+ b# a
show that the leukemic clone remains detectable, as we have previously shown in& G& U% n9 K* E" n" T
imatinib-treated patients. Dasatinib-associated immunological phenomena, such as% Y# g, Y8 ^, N' |) [
the emergence of clonal T cell populations, were observed both in one patient
6 D" `' U8 _& V" l9 C1 J2 awho relapsed and in one patient in remission. Our results suggest that the
0 f- }% [; f4 I2 g' }; Z( Hcharacteristics of complete molecular response on dasatinib treatment may be. V/ i' N2 J) h7 g3 J
similar to that achieved with imatinib, at least in patients with adverse6 \! R$ z- w! [3 }! {: ]+ O# w
disease features., \7 P) B2 g8 W6 `8 K' z
|