Mucin 16-Directed Therapy in Pediatric Sarcomas: Case Evidence of Ubamatamab Efficacy in Epithelioid Sarcoma and Its Implications for Other Sarcoma Subtypes.

IF 5.6 2区 医学 Q1 ONCOLOGY
Denise M Connolly, Gabriel Revon-Rivière, Rose Chami, Denise Mills, Ailish C Coblentz, Thomas S Uldrick, David A Knorr, Priscila Goncalves, Michael Dobosz, Sumreen Jalal, Sarah Cohen-Gogo, Daniel A Morgenstern
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引用次数: 0

Abstract

Purpose: Epithelioid sarcoma (ES) and malignant rhabdoid tumor (MRT) are rare soft tissue sarcomas with poor prognoses. Although mucin 16 (MUC16) and its soluble form, cancer antigen 125 (CA125), are established as biomarkers and therapeutic targets in ovarian cancer, emerging data suggest MUC16 may also be expressed in ES and MRT. In this study, we present a patient with ES, who demonstrated a response to ubamatamab, a novel bispecific T-cell engager (MUC16xCD3), and analyze treatment resistance after disease progression. Additionally, we examine MUC16 expression across pediatric and adolescent and young adult (AYA) sarcomas, to evaluate the frequency of this target and explore the broader application of ubamatamab in this population.

Materials and methods: We performed a retrospective clinical case review and immunohistochemical analysis of pediatric and AYA (0-25 years) sarcoma samples from 2015 to 2021, evaluating MUC16 expression using anti-CA125 immunohistochemistry (IHC) on the DAKO Omnis platform.

Results: A 23-year-old female patient with multiply relapsed metastatic ES, harboring MUC16 expression by IHC and elevated serum CA125, received intravenous ubamatamab (250 mg) once per week as part of a single patient study. After 11 weeks of ubamatamab, a RECIST v1.1 partial response was demonstrated, along with serum CA125 normalization, lasting 43 weeks. During the initial step-up dosing, the patient experienced grade 2 cytokine release syndrome. Treatment-emergent adverse events included grade 2 pleural effusion, pericardial effusion, and palmar-plantar erythrodysesthesia, all resolving without intervention. IHC analysis of retrospective samples showed positive MUC16 staining in six of eight (75%) ES and two of four (50%) MRT samples, with no immunoreactivity observed in other pediatric/AYA sarcoma subtypes.

Conclusion: MUC16 is frequently detected in ES and MRTs. Ubamatamab is an encouraging anti-MUC16 therapy, demonstrating clinical efficacy. Ongoing trials (ClinicalTrials.gov identifier: NCT06444880) are evaluating ubamatamab in other rare MUC16-positive tumors.

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粘蛋白16定向治疗儿童肉瘤:Ubamatamab对上皮样肉瘤疗效的病例证据及其对其他肉瘤亚型的影响
目的:上皮样肉瘤(ES)和恶性横纹肌样肿瘤(MRT)是一种少见的预后较差的软组织肉瘤。尽管黏液蛋白16 (MUC16)及其可溶形式癌抗原125 (CA125)已被确定为卵巢癌的生物标志物和治疗靶点,但新出现的数据表明MUC16也可能在ES和MRT中表达。在这项研究中,我们介绍了一名ES患者,他对ubamatamab(一种新型双特异性t细胞接触器(MUC16xCD3))有反应,并分析了疾病进展后的治疗耐药性。此外,我们检测了MUC16在儿童、青少年和青壮年(AYA)肉瘤中的表达,以评估这一靶点的频率,并探索ubamatamab在这一人群中的更广泛应用。材料和方法:我们对2015 - 2021年儿科和AYA(0-25岁)肉瘤样本进行了回顾性临床病例回顾和免疫组织化学分析,在DAKO Omnis平台上使用抗ca125免疫组织化学(IHC)评估MUC16的表达。结果:一名23岁的女性多发性复发转移性ES患者,IHC表达MUC16,血清CA125升高,每周静脉注射ubamatamab (250 mg)一次,作为单例患者研究的一部分。ubamatamab治疗11周后,RECIST v1.1部分缓解,血清CA125正常化,持续43周。在最初的增加剂量期间,患者经历了2级细胞因子释放综合征。治疗中出现的不良事件包括2级胸腔积液、心包积液和掌跖红肿,这些不良事件都在没有干预的情况下消失了。回顾性样本的免疫组化分析显示,8个ES样本中有6个(75%)MUC16染色阳性,4个MRT样本中有2个(50%)MUC16染色阳性,在其他儿科/AYA肉瘤亚型中未观察到免疫反应性。结论:MUC16在ES和MRTs中多见。Ubamatamab是一种令人鼓舞的抗muc16疗法,显示出临床疗效。正在进行的试验(ClinicalTrials.gov标识符:NCT06444880)正在评估ubamatamab在其他罕见muc16阳性肿瘤中的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.10
自引率
4.30%
发文量
363
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