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复发性腹膜后去分化脂肪肉瘤伴高肿瘤突变负荷对帕博利珠单抗达到病理完全缓解:一例病例报告

英文原题:Pathological complete response to pembrolizumab in recurrent retroperitoneal dedifferentiated liposarcoma with high tumor mutational burden: a case report.

PubMed 2025/11/28(内容时间) World J Surg Oncol Q1 · IF 2.8(JCR 2025)

研究概要

这是首例报道的高TMB复发性腹膜后DDLPS经pembrolizumab治疗达到pCR的病例。肿瘤微环境中高TMB和高TAM密度可能是DDLPS对ICIs应答的预测生物标志物。

研究思路结论见上方概要

去分化脂肪肉瘤(DDLPS)是腹膜后软组织肉瘤的一种常见亚型,通常对常规化疗反应有限。近年来,免疫检查点抑制剂(ICIs)在DDLPS中显示出有前景的活性。然而,预测疗效的生物标志物仍不明确。我们报告一例复发性腹膜后DDLPS,具有高肿瘤突变负荷(TMB),对帕博利珠单抗表现出病理完全缓解(pCR)。我们还探讨了ICIs疗效与肿瘤微环境之间的关联,包括程序性死亡配体1(PD-L1)、TIL(肿瘤浸润淋巴细胞)(TILs)和肿瘤相关巨噬细胞(TAMs)。病例介绍:一名73岁男性,因转移性前列腺癌接受激素治疗,在常规随访影像中偶然发现右髂窝多房性腹膜后肿瘤。他接受了肉眼完全肿瘤切除术,组织学诊断为DDLPS。八个月后,检测到腹膜播散复发。他接受了多柔比星(6个周期),随后接受帕唑帕尼(13周)和艾日布林(3个周期)。对所有这些治疗的反应均为疾病进展。原发肿瘤的综合基因组分析显示高TMB(13个突变/兆碱基)。帕博利珠单抗400 mg每6周给药一次。11个周期后,影像显示部分缓解,靶病灶缩小56.7%。然而,由于ICI诱导的炎性关节炎,需要停用帕博利珠单抗。在第二次根治性手术中,切除了9个播散病灶。组织学检查显示广泛玻璃样变和坏死,无残留存活肿瘤细胞,提示pCR。第二次手术后15个月,他仍然存活且状况良好,无疾病复发。原发肿瘤的免疫组化显示PD-L1表达阴性、TIL密度低、TAM密度显著增高。

展开英文摘要原文

BACKGROUND: Dedifferentiated liposarcoma (DDLPS), a common subtype of retroperitoneal soft tissue sarcoma, generally shows a limited response to conventional chemotherapy. Recently, immune checkpoint inhibitors (ICIs) have demonstrated promising activity against DDLPS. However, predictive biomarkers for response remain unclear. We present a case of recurrent retroperitoneal DDLPS with a high tumor mutational burden (TMB), demonstrating a pathological complete response (pCR) to pembrolizumab. We also explore the association between the response to ICIs and the tumor microenvironment, including programmed death-ligand 1 (PD-L1), tumor-infiltrating lymphocytes (TILs), and tumor-associated macrophages (TAMs). CASE PRESENTATION: A 73-year-old man undergoing hormone therapy for metastatic prostate cancer was incidentally found to have a multilobulated retroperitoneal tumor in the right iliac fossa during routine follow-up imaging. He underwent macroscopically complete removal of the tumor, which was histologically diagnosed as DDLPS. Eight months later, recurrence with peritoneal dissemination was detected. He received doxorubicin (6 cycles) followed by pazopanib (13 weeks) and eribulin (3 cycles). The response to all these treatments was progressive disease. Comprehensive genomic profiling of the primary tumor revealed high TMB (13 mutations/megabase). Pembrolizumab 400 mg was administered every 6 weeks. After 11 cycles, imaging revealed a partial response with a 56.7% decrease in target lesions. However, discontinuation of pembrolizumab was required due to ICI-induced inflammatory arthritis. In a second radical surgery, 9 disseminated lesions were excised. Histological examination showed extensive hyalinization and necrosis with no residual viable tumor cells, indicating pCR. He remains alive and well without disease 15 months after the second surgery. Immunohistochemistry of the primary tumor revealed negative PD-L1 expression, low TIL density, and markedly high TAM density. CONCLUSIONS: This is the first reported case of recurrent retroperitoneal DDLPS with high TMB achieving pCR to pembrolizumab. High TMB and high TAM density in the tumor microenvironment may be predictive biomarkers for the response to ICIs in DDLPS.

论文信息

作者
Abe S、Zhou Q、Ariizumi T、Sugai M、Kawachi Y、Ando T、Hirose Y、Ishikawa H
单位
Division of Digestive and General Surgery, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata City, 951-8510, Japan. s-abe@med.niigata-u.ac.jp.Japan
文献类型
病例报告
期刊
World journal of surgical oncology2025 Nov 28
原文标识
PubMed 41316348 · DOI 10.1186/s12957-025-04096-3