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Preliminary safety and efficacy results of laser immunotherapy for the treatment of metastatic breast cancer patients

机译:激光免疫疗法治疗转移性乳腺癌患者的初步安全性和有效性结果

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We report our preliminary results of a pilot clinical trial of late-stage breast cancer patients treated by laser immunotherapy (LIT), a local intervention using an 805 nm laser for non-invasive irradiation, indocyanine green for selective thermal effect, and immunoadjuvant (glycated chitosan) for immunological stimulation. Ten breast cancer patients were enrolled in this study; all patients were considered to be out of other available treatment options. Toxicity was individually evaluated through physical exams and laboratory tests. Adverse reactions only occurred in the area of treatment due to photothermal injury and local administration of immunoadjuvant. No grade 3 or 4 side effects were observed. Treatment efficacy of LIT was also evaluated by physical examination and tomography. In 8 patients available for evaluation, the objective response rate was 62.5% and the clinical beneficial response rate was 75%. While the study is still ongoing, the initial outcomes of this clinical trial show that LIT is well tolerated and is promising in the treatment of metastatic breast cancer.
机译:我们报告了通过激光免疫疗法(LIT)治疗的晚期乳腺癌患者的先导临床试验的初步结果,使用805 nm激光进行非侵入性照射,吲哚菁绿进行选择性热效应和免疫佐剂(糖化)的局部干预壳聚糖)用于免疫刺激。这项研究招募了十名乳腺癌患者。所有患者均被认为没有其他可用的治疗方法。毒性通过身体检查和实验室测试单独评估。由于光热损伤和免疫佐剂的局部给药,不良反应仅发生在治疗区域。没有观察到3级或4级副作用。还通过体格检查和体层摄影术评估了LIT的治疗效果。在可供评估的8例患者中,客观缓解率为62.5%,临床有益缓解率为75%。尽管这项研究仍在进行中,但这项临床试验的初步结果表明,LIT具有良好的耐受性,在治疗转移性乳腺癌方面很有希望。

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