Grupo de Inmunobiología Y Biología Celular, Facultad de Ciencias, Pontificia Universidad Javeriana, Carrera 7 No. 43-82, Edificio Félix Restrepo, Lab 101., C.P.110211, Bogotá, Colombia.
Centro Javeriano de Oncología, Hospital Universitario San Ignacio, Bogotá, Colombia.
BMC Complement Med Ther. 2023 Sep 5;23(1):309. doi: 10.1186/s12906-023-04139-w.
Chemotherapy in breast cancer is effective but can generate significant toxicity and lead to tumor resistance. Joint treatment with standardized plant extracts can be an alternative to improve the response and allow an effective activation of the antitumor immune response that favors recovery in the short and long term. The P2Et extract of Caesalpinia spinosa presents antitumor activity in cells and animal models of breast cancer, improves the tumor microenvironment, and induces activation of the specific immune response against the tumor and is synergistic when used together with anthracyclines, which makes it a good candidate for evaluation in patients.
Conducted at a single center, this phase II study is a randomized, double-blind, placebo-controlled trial aimed at assessing the safety and efficacy of P2Et extract in patients diagnosed with stage II and III breast cancer, who are eligible for neoadjuvant treatment. The study aims to determine the safety profile at the previously established optimal biological dose from phase I trial while investigating various efficacy outcomes. These outcomes include improvements in quality of life, immunomodulation, metabolic profile, microbiome, as well as clinical indicators such as tumor reduction, disease-free survival, and pathological response, assessed at different stages of the treatment regimen.
Treatment with the P2Et extract in breast cancer patients is hypothesized to enhance overall well-being, positively influencing their quality of life, while also triggering an antitumor immune response and enhancing immune infiltration. These combined effects have the potential to contribute to improved long-term survival outcomes for patients receiving the phytomedicine alongside neoadjuvant chemotherapy treatment.
This trial was registered in the US National Library of Medicine with identifier NCT05007444. First Registered August 16, 2021. Last Updated: August 9, 2022.
乳腺癌的化疗虽然有效,但会产生显著的毒性,并导致肿瘤耐药。联合使用标准化植物提取物进行治疗可能是一种替代方法,可以提高疗效,有效激活抗肿瘤免疫反应,从而在短期和长期内促进康复。金雀儿 P2Et 提取物在乳腺癌细胞和动物模型中具有抗肿瘤活性,可改善肿瘤微环境,诱导针对肿瘤的特异性免疫反应激活,与蒽环类药物联合使用具有协同作用,使其成为评估患者的良好候选药物。
这是一项在单中心进行的 II 期随机、双盲、安慰剂对照试验,旨在评估 P2Et 提取物在适合新辅助治疗的 II 期和 III 期乳腺癌患者中的安全性和疗效。该研究旨在确定之前 I 期试验中确定的最佳生物学剂量的安全性概况,同时研究各种疗效结果。这些结果包括改善生活质量、免疫调节、代谢谱、微生物组以及肿瘤缩小、无病生存和病理反应等临床指标,这些指标在治疗方案的不同阶段进行评估。
假设在乳腺癌患者中使用 P2Et 提取物治疗可以增强整体幸福感,对其生活质量产生积极影响,同时触发抗肿瘤免疫反应并增强免疫浸润。这些综合效应可能有助于改善接受植物药联合新辅助化疗治疗的患者的长期生存结果。
该试验在美国国立医学图书馆注册,标识符为 NCT05007444。首次注册日期为 2021 年 8 月 16 日,最后更新日期为 2022 年 8 月 9 日。