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小细胞肺癌转录分型对中枢神经系统转移的预后意义。

Prognostic Implications of Small Cell Lung Cancer Transcriptional Subtyping for CNS Metastases.

机构信息

Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, NY.

Department of Radiation Medicine and Applied Sciences, University of California San Diego, San Diego, CA.

出版信息

JCO Precis Oncol. 2024 Apr;8:e2300470. doi: 10.1200/PO.23.00470.

Abstract

PURPOSE

Small cell lung cancer (SCLC) often metastasizes to the brain and has poor prognosis. SCLC subtypes distinguished by expressing transcriptional factors ASCL1 or NEUROD1 have been identified. This study investigates the impact of transcription factor-defined SCLC subtype on incidence and outcomes of brain metastases (BMs).

METHODS

Patients with SCLC with ASCL1 (A) and NEUROD1 (N) immunohistochemical expression status were identified and classified: (1) A+/N-, (2) A+/N+, (3) A-/N+, and (4) A-/N-. Cumulative incidence competing risk analyses were used to assess incidence of CNS progression. Cox proportional hazards models were used for multivariable analyses of overall survival (OS) and CNS progression-free survival (CNS-PFS).

RESULTS

Of 164 patients, most were either A+/N- or A+/N+ (n = 62, n = 63, respectively). BMs were present at diagnosis in 24 patients (15%). Among them, the 12-month cumulative incidence of subsequent CNS progression was numerically highest for A+/N- (50% [95% CI, 10.5 to 74.7]; = .47). Among those BM-free at diagnosis, the 12-month cumulative incidence of CNS progression was numerically the highest for A+/N- (16% [95% CI, 7.5 to 27.9]) and A-/N+ (9.1% [95% CI, 0.0 to 34.8]; = .20). Both subtypes, A+/N- and A-/N+, had worse OS compared with A+/N+ (A+/N-: hazard ratio [HR], 1.62 [95% CI, 1.01 to 2.51]; < .05; A-/N+: HR, 3.02 [95% CI, 1.35 to 6.76]; = .007). Excellent response rates (28, 65% CR/PR) across subtypes were seen in patients who had CNS-directed radiotherapy versus systemic therapy alone (9, 36% CR/PR).

CONCLUSION

To our knowledge, this report is the first to investigate CNS-specific outcomes based on transcription factor subtypes in patients with SCLC. BM-free patients at diagnosis with A+/N- or A-/N+ subtypes had worse outcomes compared with those with transcriptional factor coexpression. Further investigation into the mechanisms and implications of SCLC subtyping on CNS-specific outcomes is warranted to ultimately guide personalized care.

摘要

目的

小细胞肺癌(SCLC)常发生脑转移,预后不良。现已确定 SCLC 亚型通过表达转录因子 ASCL1 或 NEUROD1 进行区分。本研究旨在探讨转录因子定义的 SCLC 亚型对脑转移(BM)发生率和结局的影响。

方法

确定并分类具有 ASCL1(A)和 NEUROD1(N)免疫组织化学表达状态的 SCLC 患者:(1)A+/N-,(2)A+/N+,(3)A-/N+和(4)A-/N-。使用累积发生率竞争风险分析评估中枢神经系统进展的发生率。使用 Cox 比例风险模型进行总生存(OS)和中枢神经系统无进展生存(CNS-PFS)的多变量分析。

结果

在 164 例患者中,大多数为 A+/N-或 A+/N+(n=62,n=63)。24 例患者(15%)诊断时存在 BM。其中,A+/N-的 12 个月累积 CNS 进展发生率最高(50%[95%CI,10.5 至 74.7];=.47)。在诊断时无 BM 的患者中,A+/N-的 12 个月 CNS 进展发生率最高(16%[95%CI,7.5 至 27.9])和 A-/N+(9.1%[95%CI,0.0 至 34.8];=.20)。与 A+/N+相比,A+/N-和 A-/N+两种亚型的 OS 均较差(A+/N-:风险比[HR],1.62[95%CI,1.01 至 2.51];<.05;A-/N+:HR,3.02[95%CI,1.35 至 6.76];=.007)。与单独全身治疗相比,接受中枢神经系统定向放疗的患者具有跨亚型的出色反应率(28 例,65%完全缓解/部分缓解)。

结论

据我们所知,这是第一份基于 SCLC 患者转录因子亚型调查中枢神经系统特定结局的报告。与转录因子共表达相比,诊断时无 BM 的 A+/N-或 A-/N+亚型患者的结局较差。需要进一步研究 SCLC 亚组在中枢神经系统特定结局中的机制和意义,以最终指导个体化治疗。

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