PO.CL01.22 · 临床研究

用于监测结直肠癌患者血液和脑脊液的新型CDH17 CTC检测的开发

Development of a novel CDH17 CTC assay to monitor colorectal patient blood and cerebrospinal fluid

海报缩略图:用于监测结直肠癌患者血液和脑脊液的新型CDH17 CTC检测的开发
编号 1082 展板 22 时间 4/19 02:00–05:00 区域 Section 42 主讲 Pashtoon Kasi, MD;MS
分会场 Circulating Tumor Cells, Metastasis, and Dissemination Biology 1
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作者与单位 Authors & Affiliations

Jennifer C. Chow1, Casey E. Helmicki1, Rachel Ponting1, Arturo B. Ramirez1, Pashtoon Murtaza Kasi2

1RareCyte, Inc., Seattle, WA,2City of Hope Comprehensive Cancer Ctr., Duarte, CA

摘要 Abstract

中文摘要
CDH17是一种细胞黏附分子,通常表达于肠上皮细胞和胰管中。CDH17过表达与肿瘤进展、转移及较差预后相关,目前正作为处于临床开发中的CAR-T疗法的靶点被研究。循环肿瘤细胞(CTCs)是从肿瘤脱落进入血液或其他生物体液中的完整细胞,可作为液体活检用于动态评估肿瘤蛋白表达。在本研究中,我们开发并验证了一种免疫荧光检测以测量CTCs中CDH17的表达,并实现对患者血液和脑脊液(CSF)样本中肿瘤CDH17表达的纵向监测。为优化CDH17 CTC检测,使用掺入健康供者血液的阳性和阴性细胞系筛选了多个克隆。使用Leica BOND RX自动染色仪应用的E5J8Z克隆(Cell Signaling Technologies)在阳性与阴性细胞系之间提供了最高的信噪比(S:B)。最终检测的S:B为138,区分阳性与阴性细胞的准确率为99.9%。将经验证的检测应用于从一例接受靶向CDH17的CAR-T疗法的IV期结直肠癌伴脑转移患者采集的4份纵向血液和CSF样本(见表)。 血液和CSF中均检测到CDH17(+) CTCs,同一时间点的CSF样本中CTC数量和CDH17表达高于血液。在抗CDH17 CAR-T疗法后,血液和CSF中的CTC数量和CDH17表达下降,并在后期样本中降至不可检测水平。 本研究证明了CDH17 CTC检测在一例结直肠癌(CRC)患者血液和CSF中的可行性及稳健性能。CTC数量和CDH17表达的变化可作为治疗反应的先兆,并提供了一种微创方法以纵向监测生物标志物表达。该方法可为接受CDH17靶向治疗的患者提供预测和预后洞见。 纵向CTC与CDH17监测 采血# 样本 采集日期 体积(mL) CTC# CTC#/mL CDH17 MFI CDH17阳性% 1 血液 2024年11月27日 3.8 0 0 未进行 未进行 2 血液 2025年5月20日 6.6 0 0 未进行 未进行 2 CSF 2025年5月20日 3 11 1.7 未进行 未进行 3 血液 2025年6月30日 6.1 1 0.2 9 0 3 CSF 2025年6月30日 2 4 2 3969 100 4 血液 2025年7月28日 6.6 4 0.6 47 0 4 CSF 2025年7月28日 2.9 1 0.3 84 100 5 血液 2025年8月22日 3 0 0 - - 5 CSF 2025年8月22日 2 0 0 - - 6 CSF 2025年9月2日 1 0 0 - -
查看英文原文 English abstract
CDH17 is a cell adhesion molecule typically expressed in intestinal epithelial cells and pancreatic ducts. CDH17 overexpression is linked to tumor progression, metastasis and poorer prognosis and is being investigated as a target of CAR-T therapies currently in clinical development. Circulating tumor cells (CTCs) are intact cells shed from the tumor into blood or other biological fluids and can serve as a liquid biopsy for dynamic assessment of tumor protein expression. In this study we developed and validated an immunofluorescent assay to measure CDH17 expression in CTCs, and enable longitudinal monitoring of tumor CDH17 expression in patient blood and cerebrospinal fluid (CSF) samples. To optimize the CDH17 CTC assay, multiple clones were screened using positive and negative cell lines spiked into healthy donor blood. Clone E5J8Z (Cell Signaling Technologies) applied using the Leica BOND RX autostainer, provided the highest signal-to-background (S:B) ratio between positive negative cell lines. Final assay had S:B of 138 and 99.9% accuracy in distinguishing positive from negative cells.The verified assay was applied to 4 longitudinal blood and CSF samples collected from a stage IV colorectal cancer patient with brain metastasis undergoing CAR-T therapy targeting CDH17 (see table). CDH17(+) CTCs were detected in both blood and CSF, with higher CTC numbers and CDH17 expression observed in CSF samples compared to blood from the same timepoint. CTC numbers and CDH17 expression in blood and CSF decreased upon anti-CDH17 CAR-T therapy and reached undetectable levels in later samples. This study demonstrates the feasiblity and robust performance of the CDH17 CTC assay in blood and CSF of a CRC patient. Changes in CTC number and CDH17 expression can be harbingers of response to therapy and offer a minimally invasive method to longitudinally monitor biomarker expression. This approach may offer predictive and prognostic insights for patients on CDH17-targeted therapies. Longitudinal CTC and CDH17 monitoring Draw # Sample Collection Date Volume (mL) CTC # CTC#/mL CDH17 MFI % positive CDH17 1 Blood 27NOV2024 3.8 0 0 not performed not performed 2 Blood 20MAY2025 6.6 0 0 not performed not performed 2 CSF 20MAY2025 3 11 1.7 not performed not performed 3 Blood 30JUN2025 6.1 1 0.2 9 0 3 CSF 30JUN2025 2 4 2 3969 100 4 Blood 28JUL2025 6.6 4 0.6 47 0 4 CSF 28JUL2025 2.9 1 0.3 84 100 5 Blood 22AUG2025 3 0 0 - - 5 CSF 22AUG2025 2 0 0 - - 6 CSF 2SEP2025 1 0 0 - -
利益披露 Disclosure
J. C. Chow, RareCyte Employment. C. E. Helmicki, RareCyte Employment. R. Ponting, RareCyte Employment. A. B. Ramirez, RareCyte Employment. P. M. Kasi, Elicio Other, Scientific/Advisory Board. Agenus Other, Consultancy/Advisory Board. Astellas Pharma Other, Consultancy/Advisory Board. Daiichi Sankyo/AstraZeneca Other, Consultancy/Advisory Board. Bayer Consultancy/Advisory Board. Beixon Pharmaceuticals Other, Consultancy/Advisory Board. Boston Gene Other, Consultancy/Advisory Board. Delcath Systems Other, Consultancy/Advisory Board. Eli Lilly Other, Consultancy/Advisory Board. Eisai Consultancy/Advisory Board. Elicio Therapeutics Other, Consultancy/Advisory Board. Exact Sciences Other, Consultancy/Advisory Board. Foundation Medicine Other, Consultancy/Advisory Board. Guardant Other, Consultancy/Advisory Board. Illumina Other, Consultancy/Advisory Board. IPSEN Other, Consultancy/Advisory Board. Merck/MSD Oncology Other, Consultancy/Advisory Board. Natera Other, Consultancy/Advisory Board. Agenus, Merck, Novartis ). Neogenomics, QED, Regeneron, SAGA Diagnostics, Seagen, Servier, Taiho Oncology, Tempus, Xilio Therapeutics Other, Consultancy/Advisory Board.

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