K-BASKET, TAS-117, PI3K/AKT Gene Aberration

Phase 2

Completed

• Conditions: Solid Tumor, Adult
• Interventions: Drug: TAS-117

• Registration Number: NCT03017521
• Lead Sponsor: Yonsei University

Brief Summary

The phosphatidylinositol 3-kinase (PI3K)-v-akt murine thymoma viral oncogene homolog (AKT)-mammalian target of rapamycin (mTOR) signaling pathway is one of the most frequently aberrantly regulated pathways in human tumors. TAS-117 is a highly potent and selective oral allosteric AKT inhibitor. It has high affinity for AKT1, 2, and 3 and shows potent anti-proliferative activity against multiple tumor cell lines in vivo. Therefore, we propose to conduct a phase II trial of TAS-117, potent and selective AKT inhibitor, in patients with advanced solid tumor with PI3K/AKT genetic aberrancy by NGS focusing panel in part of K-BASKET trial.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2017-01-09
• Study First Submitted QC: 2017-01-10
• Study First Posted: 2017-01-11
• Study Start: 2017-11-21
• Primary Completion: 2019-12-31
• Study Completion: 2019-12-31
• Status Verified: 2021-04
• Last Update Submitted: 2021-04-21
• Last Update Posted: 2021-04-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 13

Inclusion Criteria

1. Histologically or cytologically confirmed recurrent or advanced solid cancers with PI3K/ATK aberration
2. Progressive disease who failed to previous standard treatment.
3. At least one measurable lesion according to Response Evaluation Criteria in Solid Tumors version 1.1 criteria
4. Eastern Cooperative Oncology Group performance status 0 or 1
5. Able to take medications orally
6. Adequate organ function
7. A life expectancy of at least 60 days

Exclusion Criteria

1. Previous treatment with anti-PI3K or AKT directed therapies

2. Known hypersensitivity to any drugs similar to TAS-117 in structure or class.

3. History or current evidence of type 1 or type 2 diabetes mellitus that requires insulin and/or oral antidiabetic therapy.

4. Current evidence of retinopathy that requires ophthalmological therapy.

5. History or current evidence of cardiac arrhythmia and/or conduction abnormality.

6. Treatment with any of the following within the specified time frame prior to study drug administration:

   • Major surgery within prior 4 weeks
   • Radiation therapy for extended field within 4 weeks prior to study drug administration or limited field radiation therapy within 2 weeks prior to study drug administration.
   • Any anticancer treatment within 3 weeks prior to study drug administration (mitomycin within prior 5 weeks).

7. A serious illness or medical condition(s)

8. Unresolved toxicity of Grade >1 attributed to any prior therapies (excluding alopecia, skin pigmentation and anemia).

9. Patients with the risk of hypokalemia

10. Receiving oral steroid medication.

11. Pregnant or lactating female

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
TAS-117	TAS-117	TAS-117, 16mg, orally, daily

Primary Outcome Measures

Name	Time	Method
overall response rate	2 months

Trial Locations

Locations (1)

Severance Hospital, Yonsei University Health System; 🇰🇷 Seoul, Korea, Republic of