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Preclinical Characterization of Catabolic Pathways and Metabolism of ABBV-011, a Novel Calicheamicin-Based SEZ6-Targeting Antibody-Drug Conjugate.新型基于加利车霉素的靶向SEZ6抗体药物偶联物ABBV-011的分解代谢途径和代谢的临床前特征
Drug Metab Dispos. 2024 Jan 9;52(2):135-142. doi: 10.1124/dmd.123.001516.
2
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Thyroid. 2024 Feb;34(2):167-176. doi: 10.1089/thy.2023.0279. Epub 2023 Nov 7.
3
Thyroid Carcinoma, Version 2.2022, NCCN Clinical Practice Guidelines in Oncology.甲状腺癌临床实践指南(NCCN 指南)2022 年第 2 版。
J Natl Compr Canc Netw. 2022 Aug;20(8):925-951. doi: 10.6004/jnccn.2022.0040.
4
ABBV-011, A Novel, Calicheamicin-Based Antibody-Drug Conjugate, Targets SEZ6 to Eradicate Small Cell Lung Cancer Tumors.ABBV-011,一种新型的基于丝裂霉素的抗体药物偶联物,靶向 SEZ6 以根除小细胞肺癌肿瘤。
Mol Cancer Ther. 2022 Jun 1;21(6):986-998. doi: 10.1158/1535-7163.MCT-21-0851.
5
International Medullary Thyroid Carcinoma Grading System: A Validated Grading System for Medullary Thyroid Carcinoma.国际甲状腺髓样癌分级系统:甲状腺髓样癌的有效分级系统。
J Clin Oncol. 2022 Jan 1;40(1):96-104. doi: 10.1200/JCO.21.01329. Epub 2021 Nov 3.
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Significance of achaete-scute complex homologue 1 (ASCL1) in pulmonary neuroendocrine carcinomas; RNA sequence analyses using small cell lung cancer cells and Ascl1-induced pulmonary neuroendocrine carcinoma cells.achaete-scute complex homologue 1 (ASCL1) 在肺神经内分泌癌中的意义;使用小细胞肺癌细胞和 Ascl1 诱导的肺神经内分泌癌细胞进行 RNA 序列分析。
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Pan-cancer Convergence to a Small-Cell Neuroendocrine Phenotype that Shares Susceptibilities with Hematological Malignancies.泛癌向小细胞神经内分泌表型趋同,与血液系统恶性肿瘤具有共同易感性。
Cancer Cell. 2019 Jul 8;36(1):17-34.e7. doi: 10.1016/j.ccell.2019.06.005.
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Small cell lung cancer tumors and preclinical models display heterogeneity of neuroendocrine phenotypes.小细胞肺癌肿瘤和临床前模型表现出神经内分泌表型的异质性。
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髓样甲状腺癌中治疗靶点SEZ6的检测

Detection of SEZ6, a Therapeutic Target, in Medullary Thyroid Carcinoma.

作者信息

Xu Bin, Baine Marina K, Jungbluth Achim, Alabkaa Anas, Serrette Rene, Roy Dibisha, Rudin Charles M, Ho Alan L, Sherman Eric, Dogan Snjezana, Ganly Ian, Rekhtman Natasha, Ghossein Ronald

机构信息

Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

Department of Medical Oncology, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

出版信息

J Clin Endocrinol Metab. 2025 Jun 17;110(7):2041-2046. doi: 10.1210/clinem/dgae672.

DOI:10.1210/clinem/dgae672
PMID:39324657
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12187113/
Abstract

CONTEXT

Seizure-related 6 homolog (SEZ6) is a cDNA that is strongly associated with neuroendocrine differentiation. Recently, SEZ6 expression was found in a subset of small cell lung carcinoma (SCLC). Furthermore, ABBV-011, a novel antibody-drug conjugate targeting SEZ6 has been developed and is currently in a clinical trial for the treatment of SCLC and neuroendocrine neoplasms, including medullary thyroid carcinoma (MTC).

OBJECTIVE

We herein present the first evidence that SEZ6 is highly expressed in MTC.

METHODS

SEZ6 immuno-expression was studied in 78 MTCs and correlated with clinicopathologic characteristics, outcome, and molecular profile.

RESULTS

SEZ6 was highly expressed in primary tumors, regional recurrence, and distant metastasis. Using 2 different SEZ6 antibody clones, SC17.14 and 14E5, SEZ6 immunopositivity was seen in 91% to 93% of primary MTCs, 100% of regional recurrence, and 75% to 83% of distant metastasis. High level of SEZ6 immuno-expression determined using H score was associated with male sex, advanced stage, and extrathyroidal thyroidal extension. There was no correlation between SEZ6 expression and outcome or RET/RAS mutation status in MTC. The frequency of SEZ6 positivity in MTC without RET/RAS mutations was 83%.

CONCLUSION

SEZ6 may serve as a novel biomarker for MTCs. Although SEZ6 lacks any prognostic values in MTC, its positivity in 91% to 93% of MTCs, including MTCs without RET and RAS mutations, renders SEZ6-targeted antibody-drug conjugate therapy a promising targeted therapy for MTCs.

摘要

背景

癫痫相关6同源物(SEZ6)是一种与神经内分泌分化密切相关的互补DNA。最近,在一小部分小细胞肺癌(SCLC)中发现了SEZ6的表达。此外,一种靶向SEZ6的新型抗体药物偶联物ABBV - 011已被开发出来,目前正在进行治疗SCLC和神经内分泌肿瘤(包括甲状腺髓样癌(MTC))的临床试验。

目的

我们在此首次提供证据表明SEZ6在MTC中高表达。

方法

对78例MTC进行SEZ6免疫表达研究,并与临床病理特征、预后和分子谱相关联。

结果

SEZ6在原发性肿瘤、区域复发和远处转移中高表达。使用两种不同的SEZ6抗体克隆SC17.14和14E5,在91%至93%的原发性MTC、100%的区域复发和75%至83%的远处转移中可见SEZ6免疫阳性。使用H评分确定的高水平SEZ6免疫表达与男性、晚期和甲状腺外甲状腺延伸有关。SEZ6表达与MTC的预后或RET/RAS突变状态之间无相关性。无RET/RAS突变的MTC中SEZ6阳性频率为83%。

结论

SEZ6可能作为MTC的一种新型生物标志物。虽然SEZ6在MTC中缺乏任何预后价值,但其在91%至93%的MTC(包括无RET和RAS突变的MTC)中的阳性表达使以SEZ6为靶点的抗体药物偶联物治疗成为MTC有前景的靶向治疗方法。