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临床试验/NCT07601113
NCT07601113已完成不适用

Retrospective Survival Follow-up of Stage II/II Breast Cancer Patients Receiving PG2 Combination With Adjuvant Chemotherapy

Kun-Ming Rau5 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2026年5月27日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
66
试验地点
5

研究概览

简要总结

Astragalus polysaccharides (APS), acting as an immunomodulator, is known to modulate the tumor microenvironment and inhibit tumor growth and progression, thereby suggesting potential as an adjuvant cancer therapy to improve treatment outcomes.

PG2 (APS Injection) has completed a clinical trial (Protocol name: PG2 Treatment for Reduction of Chemotherapy-Induced Toxicity and Encouraging Compliance with Chemotherapy among Stage II/III Breast Cancer Patients Receiving Adjuvant Chemotherapy , NCT03314805, hereinafter called the parent trial) aimed to show that PG2 treatment among stage II/III breast patients under adjuvant Epirubicin and cyclophosphamide (EC) regimen in reduction of chemotherapy-induced toxicities and encouraging compliance with chemotherapy. This study will further explore whether the addition of PG2 can delay cancer recurrence or metastasis, thereby conferring substantial survival benefits for early breast cancer patients with adjuvant chemotherapy by retrospectively collecting recurrence, metastasis, and survival information from patients enrolled in the parent trial.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
20 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Patients who were previously enrolled in the [PG2 Treatment for Reduction of Chemotherapy-Induced Toxicity and Encouraging Compliance with Chemotherapy Among Stage II/III Breast Cancer Patients Receiving Adjuvant Chemotherapy/NCT03314805] study.

排除标准

  • 未提供

研究组 & 干预措施

Control

Placebo

干预措施: Placebo (Drug)

Treatment

Astragalus polysaccharides 500 mg

干预措施: Astragalus polysaccharides 500 mg (Drug)

研究者

发起方
Kun-Ming Rau
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Kun-Ming Rau

Vice Superintendent

E-DA Hospital

研究点 (5)

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