IKZF1plus alterations are not associated with outcomes in Philadelphia-positive acute lymphoblastic leukemia patients enrolled in the FBMTG ALL/MRD2008 trial

被引:6
作者
Ito, Yoshikiyo [1 ,18 ]
Ozawa, Hidetoshi [2 ]
Eto, Tetsuya [3 ]
Miyamoto, Toshihiro [4 ,5 ]
Kamimura, Tomohiko [6 ]
Ogawa, Ryosuke [7 ]
Uchida, Naoyuki [8 ]
Wake, Atsusi [9 ]
Fujisaki, Tomoaki [10 ]
Ohno, Yuju [11 ]
Takase, Ken [12 ,13 ]
Okumura, Hirokazu [14 ,15 ]
Takamatsu, Yasushi [16 ]
Kawano, Noriaki [17 ]
Akashi, Koichi [4 ]
Nagafuji, Koji [2 ]
机构
[1] Imamura Gen Hosp, Dept Hematol, Kagoshima, Japan
[2] Kurume Univ, Dept Med, Div Hematol & Oncol, Sch Med, Kurume, Japan
[3] Hamanomachi Hosp, Dept Hematol, Fukuoka, Japan
[4] Kyushu Univ, Grad Sch Med Sci, Dept Med & Bioregulatory Sci, Fukuoka, Japan
[5] Kanazawa Univ, Inst Med Pharmaceut & Hlth Sci, Fac Med, Div Hematol, Kanazawa, Japan
[6] Harasanshin Hosp, Dept Hematol, Fukuoka, Japan
[7] Japan Community Hlth Care Org JCHO Kyushu Hosp, Dept Hematol & Oncol, Kitakyushu, Japan
[8] Toranomon Gen Hosp, Dept Hematol, Tokyo, Japan
[9] Toranomon Hosp Kajigaya, Dept Hematol, Kawasaki, Japan
[10] Matsuyama Red Cross Hosp, Dept Hematol, Matsuyama, Japan
[11] Kitakyushu Municipal Med Ctr, Dept Hematol, Kitakyushu, Japan
[12] Natl Hosp Org Kyushu Med Ctr, Dept Hematol, Fukuoka, Japan
[13] Natl Hosp Org Kyushu Med Ctr, Clin Res Inst, Fukuoka, Japan
[14] Toyama Prefectural Cent Hosp, Dept Hematol, Toyama, Japan
[15] Minamisoma Municipal Gen Hosp, Dept Hematol, Minamisoma, Japan
[16] Fukuoka Univ Hosp, Dept Internal Med, Div Med Oncol Hematol & Infect Dis, Fukuoka, Japan
[17] Miyazaki Prefectural Hosp, Dept Hematol, Miyazaki, Japan
[18] Imamura Gen Hosp, Dept Hematol, 11-23 Kamoike Shin Cho, Kagoshima, Kagoshima 8900064, Japan
关键词
IKZF1(plus); Philadelphia-positive ALL; B-CELL PRECURSOR; KINASE DOMAIN MUTATIONS; IMATINIB RESISTANCE; IKZF1; DELETIONS; HYPER-CVAD; PHASE-II; CHROMOSOME; CHEMOTHERAPY; THERAPY; ADULTS;
D O I
10.1111/ejh.13972
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: The prognostic significance of IKZF1(plus) in adult Philadelphia-positive acute lymphoblastic leukemia (Ph+ ALL) patients had remained to be clarified.Methods: We conducted a prospective, multicenter study, the ALL/MRD2008 trial, and investigated the clinical significance of IKZF1(plus).Results: From December 2008 to November 2013, 38 untreated Ph+ ALL patients were enrolled. At the end of the induction, 97.4% of patients (37/38) achieved complete hematological remission, with MRD-negativity of 48.6% (18/37). There were 19 patients with IKZF1(plus), 13 with IKZF1 deletion alone (Delta IKZF1) and 4 with no IKZF1 deletions (no Delta IKZF1). The probability of 3-year DFS and OS in these Ph+ ALL patients were 50% (95% confidence interval [CI], 33-65) and 55% (95% CI, 38-69), respectively. There was no significant difference between IKZF1(plus), Delta IKZF1, and no Delta IKZF1 in DFS (47%, 54%, 75% [p = .63]) or OS (47%, 62%, NA [p = .39]).Conclusions: We revealed no relationship between IKZF1(plus) status and survival outcomes in Ph+ ALL patients treated with imatinib/dasatinib combination chemotherapy. Further investigations are warranted to clarify the prognostic significance of IKZF1(plus) in adult Ph+ ALL patients.
引用
收藏
页码:103 / 112
页数:10
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