Rates of deep molecular response by digital and conventional PCR with frontline nilotinib in newly diagnosed chronic myeloid leukemia: a landmark analysis

被引:11
|
作者
Berdeja, Jesus G. [1 ]
Heinrich, Michael C. [2 ]
Dakhil, Shaker R. [3 ]
Goldberg, Stuart L. [4 ]
Wadleigh, Martha [5 ]
Kuriakose, Philip [6 ]
Cortes, Jorge [7 ]
Radich, Jerald [8 ]
Helton, Bret [8 ]
Rizzieri, David [9 ]
Paley, Carole [10 ]
Dautaj, Ilva [10 ]
Mauro, Michael J. [11 ]
机构
[1] Sarah Cannon Res Inst, Nashville, TN USA
[2] Oregon Hlth & Sci Univ, Knight Canc Inst, VA Portland Hlth Care Syst, Portland, OR 97201 USA
[3] Canc Ctr Kansas, Wichita, KS USA
[4] Hackensack Univ Med Ctr, John Theurer Canc Ctr, Hackensack, NJ USA
[5] Dana Farber Canc Inst, Boston, MA 02115 USA
[6] Henry Ford Hlth Syst, Detroit, MI USA
[7] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[8] Fred Hutchinson Canc Res Ctr, Div Clin Res, 1124 Columbia St, Seattle, WA 98104 USA
[9] Duke Univ, Sch Med, Durham, NC USA
[10] Novartis Pharmaceut, E Hanover, NJ USA
[11] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
关键词
BCR-ABL1; chronic myeloid leukemia; deep molecular response; digital PCR; nilotinib; TREATMENT-FREE REMISSION; CHRONIC-PHASE; CML PATIENTS; FOLLOW-UP; IMATINIB; DASATINIB; DISCONTINUATION; RECOMMENDATIONS; RELAPSE; LONGER;
D O I
10.1080/10428194.2019.1590569
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ENESTnext (NCT01227577) was a single-arm, multicenter trial evaluating the rate of deep molecular response by 2?years in patients with newly diagnosed (within 6?months) chronic myeloid leukemia in chronic phase (CML-CP) treated with nilotinib 300?mg twice daily. Among 128 enrolled patients, 94 (73%) achieved major molecular response (MMR; BCR-ABL1???0.1% on the International Scale [BCR-ABL1(IS)]) and 34 (27%) achieved confirmed MR4.5 (BCR-ABL1(IS) ?0.0032% detectable or undetectable; primary endpoint) by 2?years. Three-month BCR-ABL1 levels were predictive of later responses. In exploratory analyses, digital polymerase chain reaction (PCR) detected BCR-ABL1 in 39.4% of samples from patients with confirmed MR4.5 and identified further decreases in BCR-ABL1 with continued nilotinib. Safety results, including cardiovascular events, were consistent with those in other nilotinib trials. These results further substantiate the molecular response rates associated with frontline nilotinib therapy and demonstrate the feasibility of monitoring very low BCR-ABL1 transcript levels using digital PCR.
引用
收藏
页码:2384 / 2393
页数:10
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