Light Sciences Oncology, 15405 SE 37th Street, Suite 100, Bellevue, WA 98006, USA.
Expert Opin Pharmacother. 2010 Jan;11(1):133-40. doi: 10.1517/14656560903463893.
Despite therapeutic advances, cancer remains the cause of an estimated 23% of deaths in the USA. New treatments for malignancy are greatly needed.
Talaporfin sodium is a light-activated drug that causes tissue death through induction of apoptosis. Systemic antitumor effects mediated by CD8(+) T cells have been demonstrated in preclinical studies, providing a mechanism for distant response of tumors noted in clinical trials. Talaporfin sodium is approved in Japan for early-stage endobronchial cancer. Phase I and II studies in solid tumors have shown tumor regression in patients refractory to other therapies. Phase III pivotal studies against hepatocellular carcinoma as monotherapy and liver-metastatic colorectal cancer in combination with chemotherapy are ongoing. Talaporfin sodium is also in studies in men with symptomatic benign prostatic hyperplasia. Substantial safety data from clinical trials so far indicate that the drug is well tolerated.
Talaporfin sodium has a broad safety profile and a mode of action that could affect growth in treated and untreated tumors.
Clinical and preclinical studies indicate that talaporfin sodium treatment may offer a powerful option to synergize current therapies, as well as an alternative monotherapy in treating cancer.
尽管有治疗进展,癌症仍然是美国约 23%的死亡原因。非常需要新的恶性肿瘤治疗方法。
替拉扎芬钠是一种光激活药物,通过诱导细胞凋亡导致组织死亡。临床前研究证明了 CD8(+)T 细胞介导的系统抗肿瘤作用,为临床试验中观察到的肿瘤远处反应提供了一种机制。替拉扎芬钠在日本被批准用于早期支气管内癌。在对其他治疗方法耐药的实体瘤患者中进行的 I 期和 II 期研究显示肿瘤消退。针对肝细胞癌的单药治疗和联合化疗的肝转移性结直肠癌的 III 期关键研究正在进行中。替拉扎芬钠也在有症状的良性前列腺增生男性中进行研究。迄今为止,来自临床试验的大量安全性数据表明,该药物具有良好的耐受性。
替拉扎芬钠具有广泛的安全性和作用模式,可能会影响治疗和未治疗肿瘤的生长。
临床前和临床研究表明,替拉扎芬钠治疗可能提供一种强大的选择,以协同当前的治疗方法,以及作为治疗癌症的替代单一疗法。