基于 DNA 超分子水凝胶的保护性 NK 细胞储库用于增强三阴性乳腺癌治疗
Protective NK Cell Reservoir Based on DNA Supramolecular Hydrogel for Enhanced Triple-Negative Breast Cancer Therapy.
过继性自然杀伤(NK)细胞疗法是治疗三阴性乳腺癌的一种有前景的策略,但其疗效往往受到瘤内持久性差以及在免疫抑制性肿瘤微环境中功能耗竭的限制。
英文原题:TIL-Driven De-escalated Chemotherapy in Stage I-II TNBC
这是一项 II 期注册临床试验,评估细胞治疗用于乳腺癌的安全性、可行性及初步疗效。当前状态:招募中。计划入组 40 例。试验地点:其他 · 巴西利亚、库里蒂巴、里约热内卢、萨尔瓦多(共 5 个中心)。登记号:NCT07074106。
不限性别 · ≥ 18 Years
纳入标准: • 组织学确诊原发浸润性乳腺癌。 • 符合以下任一情况: • 临床分期T1c N0 M0,TIL水平不限;或 • 临床分期T2 N0 M0,TIL≥50%。 • 雌激素受体(ER)和孕激素受体(PR)表达<10%。 • 按当前ASCO-CAP标准,HER2阴性或无扩增。 • 入组前影像学(胸/腹/盆腔CT或FDG PET-CT)无远处转移证据。 • 年龄≥18岁。 • ECOG体能状态0至2。 • 器官功能足够。 排除标准: • 存在未控制的严重合并症,包括但不限于活动性或持续性感染、不稳定型心绞痛、未控制的心律失常、充血性心力衰竭(NYHA III或IV级)、活动性缺血性心脏病或慢性肝肾疾病。 • 妊娠或哺乳期。 • 有严重过敏反应史,包括对铂类药物或紫杉烷类药物发生过敏性休克或其他超敏反应。
Inclusion Criteria: * Histologically confirmed primary invasive breast carcinoma. * One of the following conditions: * Clinical stage T1c N0 M0 with any level of TILs; or * Clinical stage T2 N0 M0 with TILs ≥ 50%. * Estrogen receptor (ER) and progesterone receptor (PR) expression \< 10%. * HER2-negative or non-amplified, according to current ASCO-CAP criteria. * No evidence of distant metastasis based on imaging performed prior to study entry (chest/abdomen/pelvis CT scan or FDG PET-CT). * Age ≥ 18 years. * ECOG performance status of 0 to 2. * Adequate organ function Exclusion Criteria: * The subject has an uncontrolled severe concomitant condition, including but not limited to: active or ongoing infection, unstable angina, uncontrolled cardiac arrhythmia, congestive heart failure (NYHA Class III or IV), active ischemic heart disease, or chronic liver or kidney disease. * Pregnant or breastfeeding participants. * History of severe allergic reactions, including anaphylaxis or other hypersensitivity reactions to platinum-based agents or taxanes.
以上为辅助阅读译文。是否适合入组须由主治医生判断,最终以登记平台与研究者确认为准。
主要终点:Pathological complete response rate after 4 cycles of Carboplatin plus Paclitaxel. · 3 mo
所有患者接受卡铂联合一种紫杉烷治疗4个周期。达到影像学完全缓解者直接手术;未达到影像学完全缓解者在手术前再接受多柔比星联合环磷酰胺,可联合或不联合帕博利珠单抗,追加4个周期。
这是一项II期临床研究,旨在为I期或II期三阴性乳腺癌女性探索更加个体化、强度较低的化疗方案。治疗方案根据免疫系统指标(肿瘤浸润淋巴细胞,TIL)及治疗期间影像学结果调整。 I期三阴性乳腺癌患者(不论TIL水平)以及TIL较高(≥50%)的II期患者,将接受卡铂联合紫杉烷治疗4个周期。 如果影像学显示治疗后肿瘤完全消失,患者将直接接受手术;如仍可见肿瘤,则增加蒽环类药物和环磷酰胺化疗,可联合或不联合帕博利珠单抗(该药可帮助免疫系统抗癌)。 研究主要目标是评估治疗后癌症完全消失的患者比例。其他目标包括了解影像学结果与手术发现的关系,以及追踪患者在癌症未复发情况下的生存时间。
This is a phase II clinical study testing a more personalized and lighter chemotherapy approach for women with stage I or II triple-negative breast cancer. The treatment is adjusted based on signs from the immune system (called tumor-infiltrating lymphocytes, or TILs) and imaging results during treatment. Patients with stage I triple-negative breast cancer (regardless of TIL levels) and those with stage II disease and high TILs (50% or more) will receive a combination of two chemotherapy drugs (carboplatin and a taxane) for four cycles. If imaging shows the tumor has completely disappeared after this treatment, the patient will go straight to surgery. If the tumor is still visible, the treatment will be strengthened with additional chemotherapy drugs (anthracycline and cyclophosphamide), with or without a medicine called pembrolizumab, which helps the immune system fight cancer. The main goal of the study is to see how many patients have a complete disappearance of the cancer after treatment. Other goals include understanding how imaging results relate to what is found during surgery and tracking how long patients live without the cancer coming back.
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