Department of Medical Oncology, Hospital Universitario 12 de Octubre, Madrid, Spain.
Virology and Inflammation Unit, PharmaMar, SA, Madrid, Spain.
Oncologist. 2023 Jun 2;28(6):e406-e415. doi: 10.1093/oncolo/oyad078.
T-cell receptor (TCR-T) therapies are based on the expression of an introduced TCR targeting a tumor associated antigen (TAA) which has been studied in several trials in cutaneous melanoma. We conducted a systematic review and meta-analysis aiming to assess the primary efficacy of TCR-based adoptive cell therapy in cutaneous melanoma.
We searched through PubMed electronic database from its inception until May 21, 2022. Primary endpoints were pooled objective response rate (ORR) and disease control rate (DCR). We conducted logistic regression analyses to identify potential predictive factors for tumor response.
From 187 patients, 50 showed an objective response (pooled ORR 28%; 95% CI, 20%-37%) and a pooled DCR of 38% (95% CI, 27%-50%). Median PFS was 2, 9 months (95% CI, 1.4-3.1). A trend toward higher PFS was demonstrated for patients treated with cancer/testis antigens targeting TCR-T cells (HR 0.91 95% CI, 0.64-1.3, P = .61) among whom, patients treated with NYESO-1 targeting TCR-T showed a significantly higher PFS (HR 0.63 95% CI, 0.64-0.98, P = .03). In addition, the number of infused cells was associated with a significantly higher likelihood of tumor response (OR 6.61; 95% CI, 1.68-21.6; P = .007).
TCR-T therapy shows promising results in terms of antitumor activity and survival similar to those reported for TILs with a significantly higher benefit for cancer/testis antigens targeting cells. Since TCR-based therapy shows advantages of great potential over classic ACT strategies, further research in solid cancers is warranted (PROSPERO ID CRD42022328011).
T 细胞受体(TCR-T)疗法基于表达针对肿瘤相关抗原(TAA)的导入 TCR,该疗法已在多项皮肤黑色素瘤临床试验中进行了研究。我们进行了一项系统评价和荟萃分析,旨在评估 TCR 为基础的过继细胞疗法在皮肤黑色素瘤中的主要疗效。
我们通过 PubMed 电子数据库进行搜索,检索时间从数据库建立至 2022 年 5 月 21 日。主要终点是汇总客观缓解率(ORR)和疾病控制率(DCR)。我们进行了逻辑回归分析,以确定肿瘤反应的潜在预测因素。
从 187 例患者中,有 50 例患者出现客观缓解(汇总 ORR 为 28%;95%CI,20%-37%),汇总 DCR 为 38%(95%CI,27%-50%)。中位无进展生存期(PFS)为 2.9 个月(95%CI,1.4-3.1)。对于接受针对 TCR-T 细胞的癌症/睾丸抗原的治疗的患者,PFS 有升高的趋势(HR 0.91,95%CI,0.64-1.3,P =.61),其中,针对 NYESO-1 的 TCR-T 治疗的患者 PFS 显著升高(HR 0.63,95%CI,0.64-0.98,P =.03)。此外,输注细胞的数量与肿瘤反应的可能性显著相关(OR 6.61;95%CI,1.68-21.6;P =.007)。
TCR-T 疗法在抗肿瘤活性和生存方面显示出有前景的结果,与 TIL 报道的结果相似,针对细胞的癌症/睾丸抗原具有显著更高的获益。由于 TCR 为基础的治疗相对于经典 ACT 策略具有很大的潜在优势,因此在实体瘤中进一步研究是必要的(PROSPERO ID CRD42022328011)。