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单倍体相合外周血干细胞治疗对复发/难治性卵巢癌的疗效

英文原题:Therapeutic effect of haploidentical peripheral blood stem cell treatment on relapsed/refractory ovarian cancer.

PubMed 2023/02/02(内容时间) Bull Cancer Q4 · IF 1.1(JCR 2025)

研究概要

haplo-PBSCs 过继治疗后的中位随访时间为 14 个月。

中文摘要

传统免疫疗法用于复发/难治性转移性卵巢癌时受到限制,因为肿瘤会造成免疫抑制。由于需要新的治疗策略改善复发/难治性转移性卵巢癌患者临床结局,本研究旨在评估单倍体相合外周血干细胞(haplo-PBSC)过继治疗的疗效。13名晚期卵巢癌患者既往接受手术和化疗后病情难治,接受由其父母或子女捐献、经白细胞介素-2活化的haplo-PBSC治疗。通过CT扫描测量肿瘤大小变化、CA-125水平和生存时间评估临床结局;采用流式细胞术检测治疗前后患者T细胞和NK细胞群体。haplo-PBSC过继治疗后中位随访14个月。末次随访时,治疗后中位总生存期为9.1个月。10名患者(76.9%)腹胀、疼痛、疲乏和食欲不振等症状缓解。治疗后前2个月,10名患者(76.9%)CA125水平下降。5名患者(38.5%)病情稳定,1名患者(8%)达到部分缓解。haplo-PBSC过继治疗后,患者T细胞群体(CD3⁺CD4⁺和CD3⁺CD8⁺)及CD3⁻CD16⁺CD56⁺ NK细胞增加。本研究显示,haplo-PBSC过继治疗与复发/难治性卵巢癌患者的抗肿瘤作用及免疫反应增强相关。

展开英文摘要原文

The traditional immunotherapy is limited on relapsed/refractory metastatic ovarian cancer because tumors cause immunosuppression. Since new therapeutic strategies to improve clinical outcomes for patients with relapsed/refractory metastatic ovarian carcinoma are needed, the aim of this study was to evaluate the therapeutic effect of haploidentical peripheral blood stem cells (haplo-PBSCs) adoptive treatment on relapsed/refractory ovarian cancer. Thirteen patients with advanced stage of ovarian cancer and refractory history after surgery and chemotherapy were treated with interleukin-2 activated haplo-PBSCs donated by their parents or children. Clinical outcomes including therapeutic response by measuring tumor size changes using CT scanning, CA-125 levels and survival times were evaluated. T and NK cell population in patients before and after treatment was detected by flow cytometry analysis. The median follow-up time after haplo-PBSCs adoptive treatment was 14 months. At the time of the last follow-up, the median overall survival after haplo-PBSCs adoptive treatment was 9.1 months. Ten patients (76.9%) achieved a relief of symptoms, including abdominal distention, ache, fatigue, and poor appetite. During the first 2 months after treatment, CA125 levels decreased in 10 patients (76.9%). Five patients (38.5%) had a stable disease and 1 patient (8%) had partial response. T cell population (CD3 + CD4 + and CD3 + CD8 + ) and CD3 - CD16 + CD56 + NK cells were increased in patients after haplo-PBSCs adoptive treatment. Our study reveals that haplo-PBSCs adoptive treatment is associated with an anti-tumor effect and increasing immune responses in patients with relapsed/refractory ovarian cancer.

论文信息

作者
Li R、Zhang D、Ren B、Cao S、Zhou L、Xiong Y、Sun Q、Ren X
第一作者单位
National Clinical Research Center for Cancer, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China; Tianjin's Clinical Research Center for Cancer, Tianjin, China; Key Laboratory of Cancer Prevention and Therapy, Tianjin, China; Key Laboratory of Cancer Immunology and Biotherapy, Tianjin, China; Department of Immunology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China; Department of Biotherapy, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China; Department of Biotherapy, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China; National Clinical Research Center for Cancer, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China.China
通讯作者单位
National Clinical Research Center for Cancer, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China; Tianjin's Clinical Research Center for Cancer, Tianjin, China; Key Laboratory of Cancer Prevention and Therapy, Tianjin, China; Key Laboratory of Cancer Immunology and Biotherapy, Tianjin, China; Department of Immunology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China; Department of Biotherapy, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China; National Clinical Research Center for Cancer-Translational Research Center for Cell Immunotherapy, Department of Cancer Immunology and Immunotherapy, Tianjin Cancer Hospital Airport Hospital, Tianjin, China. Electronic address: renxiubao@tjmuch.com.China
期刊
Bulletin du cancer2023 Mar
原文标识
PubMed 36739242 · DOI 10.1016/j.bulcan.2022.11.013