Department of Medical Oncology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, 310009, China.
Cancer Institute, Key Laboratory of Cancer Prevention and Intervention, The Second Affiliated Hospital, Ministry of Education, Zhejiang University School of Medicine, Hangzhou, 310009, China.
BMC Cancer. 2024 Aug 20;24(1):1028. doi: 10.1186/s12885-024-12810-9.
The combination of immunotherapy and antiangiogenic therapy has shown potential in the treatment of numerous malignant tumors, but limited evidence was available for soft tissue sarcomas (STS). Therefore, the aim of the present study is to assess the efficacy and safety of immunotherapy in conjunction with antiangiogenic therapy in patients diagnosed with advanced STS (aSTS).
The study enrolled patients with aSTS from January 2014 to October 2022. Eligible participants had previously received anthracycline-based chemotherapy, presented with an anthracycline-resistant sarcoma subtype, or were ineligible for anthracycline treatment due to medical conditions. Following enrollment, these patients received a combination of immunotherapy and antiangiogenic therapy. The primary endpoints were the objective response rate (ORR) and progression-free survival (PFS), while the secondary endpoints included the disease control rate (DCR), overall survival (OS), and the incidence of adverse events.
Fifty-one patients were included in this cohort study. The median duration of follow-up was 15.8 months. The ORR and DCR were 17.6%, and 76.5%, respectively. The median PFS (mPFS) was 5.8 months (95% CI: 4.8-6.8) for all patients, and the median OS had not been reached as of the date cutoff. Multivariate analysis indicated that Eastern Cooperative Oncology Group performance status of 0-1 and ≤ second-line treatment were positive predictors for both PFS and OS. Patients with alveolar soft part sarcoma or clear cell sarcoma had longer mPFS (16.2 months, 95% CI: 7.8-25.6) when compared to those with other subtypes of STS (4.4 months, 95% CI: 1.4-7.5, P < 0.001). Among the observed adverse events, hypertension (23.5%), diarrhea (17.6%), and proteinuria (17.6%) were the most common, with no treatment-related deaths reported.
The combination of immunotherapy and antiangiogenic agents showed promising efficacy and acceptable toxicity in patients with aSTS, especially those with alveolar soft part sarcoma or clear cell sarcoma.
免疫疗法与抗血管生成疗法联合应用在多种恶性肿瘤的治疗中显示出了潜力,但软组织肉瘤(STS)的相关证据有限。因此,本研究旨在评估免疫疗法联合抗血管生成疗法在晚期 STS(aSTS)患者中的疗效和安全性。
本研究纳入了 2014 年 1 月至 2022 年 10 月期间确诊为 aSTS 的患者。入组患者先前接受过蒽环类药物化疗,存在蒽环类药物耐药的肉瘤亚型,或因身体状况而不适合蒽环类药物治疗。入组后,这些患者接受免疫疗法联合抗血管生成疗法治疗。主要终点为客观缓解率(ORR)和无进展生存期(PFS),次要终点包括疾病控制率(DCR)、总生存期(OS)和不良事件发生率。
本队列研究共纳入 51 例患者。中位随访时间为 15.8 个月。ORR 和 DCR 分别为 17.6%和 76.5%。所有患者的中位 PFS(mPFS)为 5.8 个月(95%CI:4.8-6.8),截至数据截止日期,中位 OS 尚未达到。多变量分析表明,Eastern Cooperative Oncology Group 体能状态 0-1 级和≤二线治疗是 PFS 和 OS 的阳性预测因素。与其他 STS 亚型患者相比,腺泡状软组织肉瘤或透明细胞肉瘤患者的 mPFS 更长(16.2 个月,95%CI:7.8-25.6),而其他 STS 亚型患者的 mPFS 更短(4.4 个月,95%CI:1.4-7.5,P<0.001)。观察到的不良事件中,高血压(23.5%)、腹泻(17.6%)和蛋白尿(17.6%)最为常见,无治疗相关死亡报告。
免疫疗法联合抗血管生成药物在 aSTS 患者中显示出了有前景的疗效和可接受的毒性,特别是在腺泡状软组织肉瘤或透明细胞肉瘤患者中。