Connolly Denise M, Revon-Rivière Gabriel, Chami Rose, Mills Denise, Coblentz Ailish C, Uldrick Thomas S, Knorr David A, Goncalves Priscila, Dobosz Michael, Jalal Sumreen, Cohen-Gogo Sarah, Morgenstern Daniel A
Division of Hematology/Oncology, Department of Pediatrics, The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada.
Department of Pediatric Oncology, Timone Children's Hospital, APHM, Marseille, France.
JCO Precis Oncol. 2025 Aug;9:e2500404. doi: 10.1200/PO-25-00404. Epub 2025 Aug 1.
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.
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.
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.
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.
上皮样肉瘤(ES)和恶性横纹肌样瘤(MRT)是预后较差的罕见软组织肉瘤。尽管粘蛋白16(MUC16)及其可溶性形式癌抗原125(CA125)已被确立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。在本研究中,我们报告了一名ES患者,该患者对新型双特异性T细胞衔接器(MUC16xCD3)乌巴他单抗有反应,并分析了疾病进展后的治疗耐药性。此外,我们检测了儿童及青少年和青年成人(AYA)肉瘤中MUC16的表达,以评估该靶点的频率,并探索乌巴他单抗在该人群中的更广泛应用。
我们对2015年至2021年的儿童及AYA(0至25岁)肉瘤样本进行了回顾性临床病例分析和免疫组化分析,在DAKO Omnis平台上使用抗CA125免疫组化(IHC)评估MUC16的表达。
一名23岁的女性患者患有多次复发的转移性ES,免疫组化显示其表达MUC16且血清CA125升高,作为单病例研究的一部分,她每周接受一次静脉注射乌巴他单抗(250mg)。在接受乌巴他单抗治疗11周后,根据实体瘤疗效评价标准(RECIST)v1.1显示部分缓解,同时血清CA125恢复正常,持续了43周。在初始剂量递增阶段,患者出现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、心包积液和手足红斑性感觉异常,均未干预自行缓解。对回顾性样本的免疫组化分析显示,8例ES样本中有6例(75%)、4例MRT样本中有2例(50%)MUC16染色呈阳性,在其他儿童/AYA肉瘤亚型中未观察到免疫反应性。
MUC16在ES和MRT中经常被检测到。乌巴他单抗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)正在评估乌巴他单抗在其他罕见的MUC16阳性肿瘤中的疗效。