Table 1:
Drug | Combination | Tumor type | Outcome | Reference |
---|---|---|---|---|
AZD5363, KI | CT / phase 1 | mCRPC | RP2D: 320 mg BID | [152] |
Ipatasertib, KI | HAT-abiraterone / phase 2 | mCRPC | Superior antitumor activity to HT | [153] |
CT / phase II | mTNBC | Longer PFS | [154] | |
MK-2206, AI | MEK inhibitor / phase 1 | KRAS-mutated solid tumors | Durable response | [134] |
CT / phase 1 | advanced solid tumors | Well-tolerated, antitumor activity | [155] | |
CT / phase 1 | breast cancer | Antitumor activity | [156] | |
Anastrozole (aromatase inhibitor) / phase 1 | ER+ breast cancer | Well-tolerated | [157] | |
Anastrozole (aromatase inhibitor) / phase 2 | PIKCA-Mutant ER+/HER2-Breast Cancer | No advantage of the combination | [135] | |
Selumetinib (MEK inhibitor) | CRC | No objective response | [136] | |
Perifosine | RT / phase 1 | NSCLC, prostate, oesophageal, colon and bladder cancer | Recommended phase II, 150 mg/day, started one week prior to RT | [141] |
mTOR inhbitior / phase 1 | recurrent pediatric solid tumors. | Well-tolerated | [144] | |
CT / phase 2 | mCRC | Promising clinical activity | [142] | |
Nelfinavir | RT / Phase 1 | rectal cancer | Well tolerated and good tumor regression | [148] |
CRT / Phase 1 | rectal cancer | Nelfinavir 750 mg recommended phase II | [149] | |
CRT / Phase 1 | NSCLC | Acceptable toxicity and promising activity | [150] | |
CRT / Phase 1 | pancreatic cancer | Acceptable toxicity and promising activity | [151] | |
CRT / Phase 2 | pancreatic cancer | Acceptable toxicity and promising activity | [147] |
CT: chemotherapy CRT: chemoradiotherapy; RT: radiotherapy; HT: hormone therapy; NSCLC: Non-small cell lung cancer; RP2D: recommended phase II dose; mCRPC: metastatic castration resistant prostate cancer; mTNBC: metastatic triple-negative breast cancer; PFS: progression-free survival; KI: kinase inhibitor; AI: allosteric inhibitor; CRC: colorectal cancer; mCRC: metastatic colorectal cancer