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Inhibitors of the PI3K/AKT/mTOR pathway in human malignancies; trend of current clinical trials
被引:16
作者:
Davoodi-Moghaddam, Zeinab
[1
]
Jafari-Raddani, Farideh
[1
]
Delshad, Mahda
[1
,2
]
Pourbagheri-Sigaroodi, Atieh
[1
]
Bashash, Davood
[1
]
机构:
[1] Shahid Beheshti Univ Med Sci, Sch Allied Med Sci, Dept Hematol & Blood Banking, Tehran, Iran
[2] Zanjan Univ Med Sci, Sch Allied Med Sci, Dept Lab Sci, Zanjan, Iran
关键词:
Phosphoinositide;
3-kinase;
PI3K inhibitor;
PI3K;
Akt;
mTOR pathway;
Targeted therapy;
Cancer;
Clinical trial;
PI3K PATHWAY;
PHOSPHATIDYLINOSITOL;
3-KINASE;
SIGNALING PATHWAY;
AKT;
CARCINOMA;
CANCER;
D O I:
10.1007/s00432-023-05277-x
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
The phosphoinositide 3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR) signaling pathway regulates proliferation, survival and metabolism, and its dysregulation is one of the most frequent oncogenic events across human malignancies. Over the last two decades, there has been significant focus on the clinical development of PI3K pathway inhibitors. More than 40 different inhibitors of this axis have reached various stages of clinical trials, but only a few of them have been approved by the Food and Drug Administration (FDA) for cancer treatment. These clinical results, however, could be improved given the importance of PI3K signaling in cancer and its role in linking cancer growth with metabolism. In this systematic review, after a glance at PI3K/AKT/mTOR pathway and its different inhibitors, we retrieved registered clinical trials evaluating the efficacy and safety of PI3K/AKT/mTOR inhibitors on Clinicaltrials.gov. Following the extraction of the data, finally we analyzed 2250 included studies in multiple steps, beginning with an overview and moving on to the details about type of malignancies, inhibitors, and treatment strategies. We also took a closer look at more than 100 phase III-IV clinical trials to pinpoint promising therapies, hoping that presenting a comprehensive picture of current clinical trials casts a flash of light on what remains to be done in future clinical trials of PI3K/AKT/mTOR inhibitors in human malignancies.
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页码:15293 / 15310
页数:18
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