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BCR-ABL halving time indicates CML prognosis during front-line TKI
Posted in: Medical Research News
Published on April 21, 2016 at 5:15 PM
By Lynda Williams, Senior medwireNews Reporter
Calculating halving time of the BCR-ABL transcript after 3 months may help determine prognosis in chronic myeloid leukaemia (CML) patients undergoing first-line tyrosine kinase inhibitor (TKI) therapy, say researchers.
Of 50 chronic phase CML patients beginning imatinib (n=33), nilotinib (n=10), dasatinib (n=4) or rotational nilotinib and imatinib (n=3) treatment, 68% achieved a BCR-ABL transcript ratio of 10% or less at the 3-month checkpoint.
Major molecular remission at 12 months, defined as a BCR-ABL transcript ratio of 0.1% or less, was achieved by 63% of the patients with a BCR-ABL transcript ratio of 10% or less at 3 months but none of the patients who had a higher transcript ratio at this time point.
Patients with a BCR-ABL transcript ratio of 10% or less were also a significant 84% more likely to achieve long-term deep molecular remission than those with a higher transcript ratio at 3 months.
After a median on-therapy follow-up of 61.8 months, event-free survival (EFS) was significantly more common in the patients with a BCR-ABL transcript rato of 10% or lower at 3 months than those with a higher ratio, with events reporte in 12% and 63%, respectively.
Analysis indicated that a halving time threshold of 17 days was 75% specific and 92% sensitive for the discrimination of patients who would achieve molecular remission, report Carmen Fava, from the University of Turin in Italy, and co-workers.
None of the patients who had a BCR-ABL transcript ratio greater than 10% at 3 months achieved a halving time of 17 days or less, the team notes in Clinical Lymphoma, Myeloma and Leukemia.
Indeed, EFS was 96% for patients with a BCR-ABL transcript ratio of 10% or less and a halving time of 17 days or less, falling significantly to 60% for those with a BCR-ABL transcript ratio of 10% or less and a halving time over 17 days, and just 27% for those with a BCR-ABL transcript ratio greater than 10%.
The authors therefore conclude: "Our data revealed that the use of ABL as a control gene is reliable for the determination of the halving time in the clinical setting, and highlight the importance of measuring the BCR-ABL transcript at the time of CML diagnosis."
BCR-ABL halving time indicates CML prognosis during front-line TKI
Started by
soundoff
, May 01 2016 04:25 AM
1 reply to this topic
#1
Posted 01 May 2016 - 04:25 AM
#2
Posted 02 May 2016 - 11:53 PM
See post of April 5 from buzzm on same article. Good comment strung follows
Diagnosed 1/15/15
FISH 92%
BMB 9:22 translocation
1/19/15 began 400 mg gleevec
1/22/15 bcr 37.2 IS
2/6/15 bcr 12.5 IS
3/26/15 bcr 10.3 IS
6/29/15 bcr 7.5 IS
9/24/15 bcr 0.8 IS
1/4/16 bcr 0.3 IS
Started 100 mg dasatinib, mutation analysis negative
4/20/16 bcr 0.03 IS
8/8/16 bcr 0.007 IS
12/6/16 bcr 0.002 IS
Lowered dasatinib to 70 mg
4/10/17 bcr 0.001 IS
Lowered dasatinib to 50 mg
7/5/17 bcr 0.004 IS
8/10/17 bcr 0.001. Stopped TKI in prep for September surgery.
9/10/17 bcr 0.006
10/10/17 bcr 0.088
FISH 92%
BMB 9:22 translocation
1/19/15 began 400 mg gleevec
1/22/15 bcr 37.2 IS
2/6/15 bcr 12.5 IS
3/26/15 bcr 10.3 IS
6/29/15 bcr 7.5 IS
9/24/15 bcr 0.8 IS
1/4/16 bcr 0.3 IS
Started 100 mg dasatinib, mutation analysis negative
4/20/16 bcr 0.03 IS
8/8/16 bcr 0.007 IS
12/6/16 bcr 0.002 IS
Lowered dasatinib to 70 mg
4/10/17 bcr 0.001 IS
Lowered dasatinib to 50 mg
7/5/17 bcr 0.004 IS
8/10/17 bcr 0.001. Stopped TKI in prep for September surgery.
9/10/17 bcr 0.006
10/10/17 bcr 0.088
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