Deep molecular responses achieved in chronic myeloid leukemia in chronic phase patients with BCR-ABL1 >10% at 3 months who are early switched to nilotinib

被引:2
|
作者
Yue, Yanhua [1 ]
Gui, Xiaomin [1 ]
He, Xuefeng [1 ]
Chen, Yan [1 ]
Pan, Jinlan [1 ]
Qiu, Huiying [1 ]
Wu, Depei [1 ]
Chen, Suning [1 ,3 ]
Guo, Lingchuan [2 ]
Cen, Jiannong [1 ]
机构
[1] Soochow Univ, Affiliated Hosp 1, Key Lab Thrombosis & Hemostasis, Jiangsu Inst Hematol,Minist Hlth, Suzhou, Peoples R China
[2] Soochow Univ, Affiliated Hosp 1, Dept Pathol, 188 Shizi St, Suzhou 215006, Jiangsu, Peoples R China
[3] Soochow Univ, Collaborat Innovat Ctr Hematol, Suzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Chronic myeloid leukemia in chronic phase; Imatinib; Nilotinib; TYROSINE KINASE INHIBITORS; EUROPEAN LEUKEMIANET; TRANSCRIPT LEVELS; CLINICAL-TRIALS; FOLLOW-UP; IMATINIB; RECOMMENDATIONS; DEFINITIONS; SURVIVAL; OUTCOMES;
D O I
10.1179/1607845415Y.0000000034
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: There are still controversies about whether or when to change therapy for those chronic myeloid leukemia in chronic phase (CML-CP) patients with BCR-ABL1 transcript level at 3 months higher than 10%. Here we studied the clinical significance of early switching to nilotinib in CML-CP patients with BCR-ABL1 >10% at 3 months. Methods: We investigated 495 first-line imatinib-treated patients with CML-CP and identified 117 (23.6%) patients with BCR-ABL1 >10% at 3 months, including 46 patients with warning response defined according to ELN-2013 recommendations. In 46 patients with warning response, 26 of them continued imatinib therapy and 20 patients early switched to nilotinib therapy. Results: Compared to continued imatinib group, nilotinib group showed significantly higher percentage achieving BCR-ABL1 <1% at 6 months (85.0% vs. 19.2%, P = 0.0004), better cumulative rates of MR3.0 and MR4.0 of 4 years (82.1% vs. 41.2%, P = 0.0091; 61.5% vs. 18.6%, P = 0.035). Conclusion: In summary, early switching to nilotinib enabled more CML-CP patients with warning molecular response at 3 months to achieve early and deeper molecular response vs. remaining on imatinib.
引用
收藏
页码:213 / 217
页数:5
相关论文
共 50 条
  • [1] OUTCOMES OF CHRONIC PHASE CHRONIC MYELOID LEUKEMIA PATIENTS WITH 10%≤AND&gt;10% BCR-ABL1 (IS) TRANSCRIPT LEVELS AFTER 3 MONTHS OF GENERIC IMATINIB TREATMENT
    Baslar, Z.
    Eskazan, A. E.
    Ayer, M.
    Kantarcioglu, B.
    Demirel, N.
    Aydin, D.
    Aydinli, F.
    Yokus, O.
    Sadri, S.
    Erdogan, I.
    Berk, S.
    Yalniz, F. F.
    Elverdi, T.
    Salihoglu, A.
    Ar, M. C.
    Aydin, S. Ongoren
    Aydin, Y.
    Tuzuner, N.
    Ozbek, U.
    Soysal, T.
    HAEMATOLOGICA, 2015, 100 : 439 - 440
  • [2] Prediction for sustained deep molecular response of BCR-ABL1 levels in patients with chronic myeloid leukemia in chronic phase
    Sasaki, Koji
    Kantarjian, Hagop
    O'Brien, Susan
    Ravandi, Farhad
    Konopleva, Marina
    Borthakur, Gautam
    Garcia-Manero, Guillermo
    Wierda, William
    Daver, Naval
    Ferrajoli, Alessandra
    Takahashi, Koichi
    Jain, Preetesh
    Rios, Mary Beth
    Pierce, Sherry
    Jabbour, Elias
    Cortes, Jorge E.
    CANCER, 2018, 124 (06) : 1160 - 1168
  • [3] Chronic Myeloid Leukemia: Beyond BCR-ABL1
    Zhou, Ting
    Medeiros, L. Jeffrey
    Hu, Shimin
    CURRENT HEMATOLOGIC MALIGNANCY REPORTS, 2018, 13 (06) : 435 - 445
  • [4] Dynamics of BCR-ABL1 transcripts during nilotinib therapy in patients with chronic myeloid leukemia (CML)
    Quintas-Cardama, Alfonso
    Kantarjian, Hagop
    Jones, Dan
    O'Brien, Susan
    Rios, Mary Beth
    Cortes, Jorge
    BLOOD, 2007, 110 (11) : 870A - 870A
  • [5] Chronic Myeloid Leukemia: Beyond BCR-ABL1
    Ting Zhou
    L. Jeffrey Medeiros
    Shimin Hu
    Current Hematologic Malignancy Reports, 2018, 13 : 435 - 445
  • [6] CLINICAL SIGNIFICANCE OF EARLY MOLECULAR RESPONSES (BCR-ABL1 ≤10% AT 3 MONTHS AND ≤1% 6 MONTHS) AS A PREDICTOR FOR LONG-TERM OUTCOMES IN CHRONIC MYELOID LEUKEMIA PATIENTS TREATED WITH IMATINIB
    Lee, S.
    Choi, S.
    Kim, S.
    Bang, J.
    Oh, Y.
    Park, J.
    Jeon, H.
    Jang, E.
    Kim, D.
    HAEMATOLOGICA, 2013, 98 : 299 - 300
  • [7] Rapid initial decline in BCR-ABL1 is associated with superior responses to second-line nilotinib in patients with chronic-phase chronic myeloid leukemia
    Stein, Andrew M.
    Martinelli, Giovanni
    Hughes, Timothy P.
    Mueller, Martin C.
    Beppu, Lan
    Gottardi, Enrico
    Branford, Susan
    Soverini, Simona
    Woodman, Richard C.
    Hochhaus, Andreas
    Kim, Dong-Wook
    Saglio, Giuseppe
    Radich, Jerald P.
    BMC CANCER, 2013, 13
  • [8] Rapid initial decline in BCR-ABL1 is associated with superior responses to second-line nilotinib in patients with chronic-phase chronic myeloid leukemia
    Andrew M Stein
    Giovanni Martinelli
    Timothy P Hughes
    Martin C Müller
    Lan Beppu
    Enrico Gottardi
    Susan Branford
    Simona Soverini
    Richard C Woodman
    Andreas Hochhaus
    Dong-Wook Kim
    Giuseppe Saglio
    Jerald P Radich
    BMC Cancer, 13
  • [9] Dasatinib rapidly induces deep molecular response in chronic-phase chronic myeloid leukemia patients who achieved major molecular response with detectable levels of BCR-ABL1 transcripts by imatinib therapy
    Shiseki, Masayuki
    Yoshida, Chikashi
    Takezako, Naoki
    Ohwada, Akira
    Kumagai, Takashi
    Nishiwaki, Kaichi
    Horikoshi, Akira
    Fukuda, Tetsuya
    Takano, Hina
    Kouzai, Yasuji
    Tanaka, Junji
    Morita, Satoshi
    Sakamoto, Junichi
    Sakamaki, Hisashi
    Inokuchi, Koiti
    INTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY, 2017, 22 (05) : 972 - 979
  • [10] Dasatinib rapidly induces deep molecular response in chronic-phase chronic myeloid leukemia patients who achieved major molecular response with detectable levels of BCR-ABL1 transcripts by imatinib therapy
    Masayuki Shiseki
    Chikashi Yoshida
    Naoki Takezako
    Akira Ohwada
    Takashi Kumagai
    Kaichi Nishiwaki
    Akira Horikoshi
    Tetsuya Fukuda
    Hina Takano
    Yasuji Kouzai
    Junji Tanaka
    Satoshi Morita
    Junichi Sakamoto
    Hisashi Sakamaki
    Koiti Inokuchi
    International Journal of Clinical Oncology, 2017, 22 : 972 - 979