a Department of Leukemia , The University of Texas at MD Anderson Cancer Center , Houston , TX , USA.
b Department of Hematology , Davidoff Cancer Center at Rabin Medical Center, Sackler School of Medicine, Tel Aviv University, Tel Aviv , Israel.
Leuk Lymphoma. 2019 Jan;60(1):37-48. doi: 10.1080/10428194.2018.1464158. Epub 2018 May 9.
As new drugs targeting MYC show clinical activity in acute myeloid leukemia (AML), understanding MYC expression in AML is of critical importance. We assessed MYC protein expression by immunohistochemistry in bone marrow of patients with untreated AML (n = 265). Overall, 90% of patients demonstrated MYC overexpression and MYC immunopositivity ≤6% was associated with superior complete remission (CR) duration of 23 months versus 12 months for MYC immunopositivity >6% (p = .028). Among 241 patients at higher risk for relapse, including those ≥55 years of age and patients with intermediate- and high-risk AML, MYC immunopositivity ≤6% conferred significantly superior median overall survival (OS) (24 versus 13 months; p = .042), event-free survival (EFS) (14 versus 6 months; p = .048), and relapse-free survival (RFS) (25 versus 12 months; p = .024). The prognostic impact of MYC-immunopositivity was retained on multivariate analysis of OS, EFS, and RFS. We conclude that MYC immunopositivity is an important prognostic factor in patients with untreated AML, particularly those at higher risk for relapse.
随着针对 MYC 的新型药物在急性髓系白血病(AML)中显示出临床活性,了解 AML 中的 MYC 表达至关重要。我们通过免疫组织化学评估了未经治疗的 AML 患者骨髓中的 MYC 蛋白表达(n=265)。总体而言,90%的患者表现出 MYC 过表达,MYC 免疫阳性率≤6%与更好的完全缓解(CR)持续时间 23 个月相关,而 MYC 免疫阳性率>6%为 12 个月(p=0.028)。在 241 名复发风险较高的患者中,包括年龄≥55 岁和中高危 AML 的患者,MYC 免疫阳性率≤6%显著改善了中位总生存期(OS)(24 个月 vs. 13 个月;p=0.042)、无事件生存期(EFS)(14 个月 vs. 6 个月;p=0.048)和无复发生存期(RFS)(25 个月 vs. 12 个月;p=0.024)。在 OS、EFS 和 RFS 的多变量分析中,MYC-免疫阳性的预后影响仍然存在。我们得出结论,MYC 免疫阳性是未经治疗的 AML 患者,尤其是复发风险较高的患者的重要预后因素。