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Phase Ib Dose-Finding Study of Varlitinib Combined with Weekly Paclitaxel With or Without Carboplatin ± Trastuzumab
Matilda Xinwei Lee1, Andrea L A Wong1,2, Samuel Ow1
1Department of Haematology-Oncology, National University Cancer Institute, Level 7, NUHS Tower Block, 1E Kent Ridge Road, Singapore, 119228, Singapore.
Background:
Varlitinib is a highly potent, small-molecule, pan-HER inhibitor targeting HER1, HER2, and HER4. It has demonstrated activity in gastric, biliary tract, and breast cancers.
Objective:
We conducted a phase Ib dose confirmation study to determine safety and early efficacy signals of varlitinib in combination with chemotherapy (paclitaxel ± carboplatin) ± subcutaneous trastuzumab.
Methods:
Eligible patients had advanced or metastatic solid tumors. A 3+3 dose de-escalation study design was used and pharmacokinetic analyses of varlitinib and paclitaxel were performed.
Results:
Thirty-seven patients were enrolled into eight cohorts with median 4 (0-14) prior lines of palliative systemic therapies. Carboplatin area under the curve 1.5 and paclitaxel 80 mg/m2 weekly with varlitinib 500 mg twice daily continuously was de-escalated over four dose levels to 300 mg twice daily intermittently (4 days on, 3 days off) due to dose-limiting toxicities, most commonly neutropenia, febrile neutropenia, and electrolyte disturbances, with the triplet combination deemed intolerable and unable to be developed further. Varlitinib was then combined with paclitaxel alone; the recommended phase II dose of varlitinib was 300 mg twice daily intermittently. The addition of subcutaneous trastuzumab 600 mg was safe with no dose-limiting toxicities. Thirty-one patients were evaluable for response: 35.5% partial response, 41.9% stable disease. Twenty patients had HER2+ metastatic breast cancer with a median of 4 (0-14) treatment lines, 8/20 continued on single-agent varlitinib after completing chemotherapy for a median of 5.1 (range 2.0-13.3) months. A pharmacokinetic analysis showed that plasma exposure of varlitinib was dose dependent. Varlitinib administration did not significantly affect the maximum concentration or area under the curve of paclitaxel.
Conclusions:
The recommended phase II dose of varlitinib with paclitaxel is 300 mg twice daily intermittently dosed. This is active in HER2+ metastatic breast cancer. Subcutaneous trastuzumab can be added safely to varlitinib and paclitaxel. This combination is currently being evaluated as neoadjuvant therapy in HER2+ breast cancer (NCT02396108).
Clinical Trial Registration:
NCT02396108, date of registration: 25 March, 2015.
Insights
Varlitinib combined with paclitaxel showed activity in HER2+ metastatic breast cancer, establishing a recommended Phase II dose. Subcutaneous trastuzumab can be safely added to this combination.
Area of Science:
- Oncology
- Pharmacology
- Clinical Trials
Background:
- Varlitinib is a potent small-molecule pan-HER inhibitor with activity in various cancers.
- It targets HER1, HER2, and HER4, making it a potential therapeutic agent for HER-driven malignancies.
Purpose of the Study:
- To determine the safety and efficacy of varlitinib in combination with chemotherapy.
- To establish the recommended Phase II dose of varlitinib for further clinical development.
Main Methods:
- A Phase Ib dose de-escalation study using a 3+3 design.
- Patients with advanced or metastatic solid tumors received varlitinib with paclitaxel ± carboplatin ± subcutaneous trastuzumab.
Main Results:
- The triplet combination of varlitinib, paclitaxel, and carboplatin was not well-tolerated due to dose-limiting toxicities.
- The recommended Phase II dose of varlitinib was determined to be 300 mg twice daily intermittently when combined with paclitaxel.
- The combination demonstrated activity in HER2+ metastatic breast cancer, with 35.5% partial response and 41.9% stable disease.
Conclusions:
- The recommended Phase II dose of varlitinib with paclitaxel is 300 mg twice daily intermittently.
- Varlitinib in combination with paclitaxel and subcutaneous trastuzumab is safe and active in HER2+ metastatic breast cancer.
- This combination is currently under investigation as neoadjuvant therapy for HER2+ breast cancer.
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