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| ID | Type | Description | Link |
|---|---|---|---|
| KEYNOTE-A91 | Other Identifier | Merck & Co. |
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| Name | Class |
|---|---|
| Merck Sharp & Dohme LLC | INDUSTRY |
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Patients with refractory metastatic colorectal cancer or non-small cell lung cancer with liver metastasis treated with Trans-arterial Tirapazamine Embolization along with Pembrolizumab.
This study is an open-label study to treat patients with refractory metastatic colorectal cancer and non-small cell lung cancer with liver metastasis. Patients enrolled in the mCRC cohort will be randomized to receive study treatment Trans-arterial Tirapazamine Embolization (TATE)+Pembrolizumab or FDA-approved standard of care, such as TAS-102 or regorafenib, and their Overall Survival (OS) will be compared in the two cohorts as the primary endpoint. Patients enrolled in the NSCLC cohort will all receive study treatment TATE+Pembrolizaumb and Overall Response Rate (ORR) will be the primary endpoint.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| colorectal cancer | Experimental | metastatic colorectal cancer progressed on at least two lines of chemotherapy |
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| NSCLC | Experimental | Liver metastatic NSCLC progressed on immune checkpoint inhibitors and chemotherapy |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| TATE and pembrolizumab | Drug | All liver metastatic lesions will be treated with TATE for maximally debulking. Pembrolizumab IV infusion per standard schedule every 3 or 6 weeks until progression or maximally 2 years. |
| Measure | Description | Time Frame |
|---|---|---|
| Overall Survival for the mCRC cohort | From the first day of treatment to death | 24 months |
| Overall Response Rate (ORR) for the NSCLC cohort | Per RECIST 1.1 criteria | within 24 months |
| Measure | Description | Time Frame |
|---|---|---|
| Duration of Response | per RECIST 1.1 | 24 months |
| Response rate | in TATE treated or TATE-untreated lesions by RECIST and mRECIST | 24 months |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Ray Lee, MD. PhD. | Contact | 8043341076 | ray.lee01@teclison.com | |
| Chiwei Lu | Contact | chiwei.lu4@teclison.com |
| Name | Affiliation | Role |
|---|---|---|
| Ray Lee | Teclison Limited | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of California, Irvine Medical Center | Recruiting | Orange | California | 92868 | United States |
International meeting report or medical Journal publication
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| ID | Term |
|---|---|
| D015179 | Colorectal Neoplasms |
| D008175 | Lung Neoplasms |
| ID | Term |
|---|---|
| D007414 | Intestinal Neoplasms |
| D005770 | Gastrointestinal Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
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| ID | Term |
|---|---|
| C582435 | pembrolizumab |
| C000613803 | trifluridine tipiracil drug combination |
| C559147 | regorafenib |
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Open-label study in two indications. The mCRC cohort will be a randomized trial for TATE+Pembrolizumab versus standard 3rd line therapy for mCRC. The NSCLC cohort will be single-arm study.
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| TAS-102 pill | Drug | The comparator of the mCRC arm is TAS-102 at 60 mg BID 5 days per week for 2 weeks then 2 weeks off. |
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| Regorafenib Pill | Drug | As an alternative to TAS-102 per treating physician's discretion. If selected, Regorafenib 160 mg oral daily for 3 weeks on and one week off, every 4 weeks per cycle. Do not take Regoarefnib if taking TAS-102. |
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| PFS | Progression Free Survival | 24 months |
| TTP | Time to Progression | 24 months |
| China Medical University Hsinchu Hospital | Recruiting | Hsinchu | Taiwan |
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| Chung Shan Medical University Hospital | Recruiting | Taichung | Taiwan |
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| D009369 | Neoplasms |
| D004066 | Digestive System Diseases |
| D005767 | Gastrointestinal Diseases |
| D003108 | Colonic Diseases |
| D007410 | Intestinal Diseases |
| D012002 | Rectal Diseases |
| D012142 | Respiratory Tract Neoplasms |
| D013899 | Thoracic Neoplasms |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |