Expression of CD56 is an unfavorable prognostic factor for acute promyelocytic leukemia with higher initial white blood cell counts

被引:34
作者
Ono, Takaaki [1 ]
Takeshita, Akihiro [1 ]
Kishimoto, Yuji [2 ]
Kiyoi, Hitoshi [3 ]
Okada, Masaya [4 ]
Yamauchi, Takahiro [5 ]
Emi, Nobuhiko [6 ]
Horikawa, Kentaro [7 ]
Matsuda, Mitsuhiro [8 ]
Shinagawa, Katsuji [9 ]
Monma, Fumihiko [10 ]
Ohtake, Shigeki [11 ]
Nakaseko, Chiaki [12 ]
Takahashi, Masatomo [13 ]
Kimura, Yukihiko [14 ]
Iwanaga, Masako [15 ]
Asou, Norio [16 ]
Naoe, Tomoki [3 ]
机构
[1] Hamamatsu Univ, Sch Med, Dept Internal Med, Hamamatsu, Shizuoka 4312102, Japan
[2] Kansai Med Univ, Dept Internal Med 1, Moriguchi, Osaka 570, Japan
[3] Nagoya Univ, Grad Sch Med, Dept Hematol Oncol, Nagoya, Aichi 4648601, Japan
[4] Hyogo Coll Med, Dept Internal Med, Div Hematol, Nishinomiya, Hyogo 6638501, Japan
[5] Univ Fukui, Dept Internal Med 1, Fukui 910, Japan
[6] Fujita Hlth Univ, Sch Med, Dept Hematol, Toyoake, Aichi 47011, Japan
[7] Kumamoto Univ, Sch Med, Dept Hematol, Kumamoto 860, Japan
[8] Kinki Univ, Sch Med, Dept Hematol, Osaka 589, Japan
[9] Okayama Univ, Grad Sch, Dept Hematol & Oncol, Okayama, Japan
[10] Mie Univ, Grad Sch Med, Dept Hematol, Tsu, Mie 514, Japan
[11] Kanazawa Univ, Grad Sch Med Sci, Dept Hematol, Kanazawa, Ishikawa, Japan
[12] Chiba Univ Hosp, Dept Hematol, Chiba, Japan
[13] St Marianna Univ, Sch Med, Div Hematol & Oncol, Kawasaki, Kanagawa, Japan
[14] Tokyo Med Univ, Ctr Hlth Surveillance & Prevent Med, Tokyo 1608402, Japan
[15] Jikei Univ, Hlth Care Ctr, Sch Med, Tokyo, Japan
[16] Saitama Med Univ, Int Med Ctr, Dept Hematol, Saitama, Japan
关键词
Acute promyelocytic leukemia; all-trans retinoic acid; CD56; expression; chemotherapy; prognostic factor; TRANS-RETINOIC ACID; ACUTE MYELOID-LEUKEMIA; ARSENIC TRIOXIDE; CONSOLIDATION; REMISSION; SURVIVAL; DIFFERENTIATION; CHEMOTHERAPY; IDARUBICIN; INDICATOR;
D O I
10.1111/cas.12319
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Expression of CD56 has recently been introduced as one of the adverse prognostic factors in acute promyelocytic leukemia (APL). However, the clinical significance of CD56 antigen in APL has not been well elucidated. We assessed the clinical significance of CD56 antigen in 239 APL patients prospectively treated with all-trans retinoic acid and chemotherapy according to the Japan Adult Leukemia Study Group APL97 protocol. All patients were prospectively treated by the Japan Adult Leukemia Study Group APL97 protocol. The median follow-up period was 8.5years. Positive CD56 expression was found in 23 APL patients (9.6%). Expression of CD56 was significantly associated with lower platelet count (P=0.04), severe disseminated intravascular coagulation (P=0.04), and coexpression of CD2 (P=0.03), CD7 (P=0.04), CD34 (P<0.01) and/or human leukocyte antigen-DR (P<0.01). Complete remission rate and overall survival were not different between the two groups. However, cumulative incidence of relapse and event-free survival (EFS) showed an inferior trend in CD56(+) APL (P=0.08 and P=0.08, respectively). Among patients with initial white blood cell counts of 3.0x10(9)/L or more, EFS and cumulative incidence of relapse in CD56(+) APL were significantly worse (30.8% vs 63.6%, P=0.008, and 53.8% vs 28.9%, P=0.03, respectively), and in multivariate analysis, CD56 expression was an unfavorable prognostic factor for EFS (P=0.04). In conclusion, for APL with higher initial white blood cell counts, CD56 expression should be regarded as an unfavorable prognostic factor.
引用
收藏
页码:97 / 104
页数:8
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