A Study of Sunitinib in Patients With Metastatic or Recurrent Thymic Carcinoma

NCT ID: NCT02623127

Last Updated: 2019-01-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 25 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-10-31
• Study Completion Date: 2018-10-31

Brief Summary

This study aims to investigate the clinical activity of sunitinib in patients with advanced thymic carcinoma who have failed chemotherapy.

Detailed Description

Sunitinib (Sutent®; Pfizer, New York, NY, USA) is a multitargeted tyrosine-kinase inhibitor (TKI) with activity against the stem cell-factor receptor (KIT) and platelet-derived growth-factor receptor (PDGFR), vascular endothelial growth-factor receptor (VEGFR), glial cell line-derived neurotrophic factor receptor (rearranged during transfection [RET]), colony-stimulating factor-1 receptor (CSF1R), and Fms-like tyrosine kinase-3 receptor (FLT3).

Sunitinib is a potent inhibitor of mutant KIT with additional inhibitory effects on VEGF receptors that potentially might make it more effective than imatinib against TCs. In the current version of NCCN guideline, sunitinib is suggested as one of the potential targeted therapeutics for advanced TCs.

We planned this study to investigate the clinical efficacy and tolerability of sunitinib in patients with advanced or recurrent TCs in Korean population. In addition, we will collect tumor samples and blood samples from patients for the further exploration of predictive biomarkers.

Conditions

Thymic Carcinoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Sunitinib

Sunitinib will be administered orally at a dose of 50 mg once daily in 3-week cycles consisting of 2 weeks of treatment followed by 1 week without treatment.

Group Type: EXPERIMENTAL

Sunitinib

Intervention Type: DRUG

Interventions

Sunitinib

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Provision of signed, written and dated informed consent prior to any study specific procedures

2. Histopathologically confirmed metastatic or recurrent thymic thymic carcinoma

3. Age ≥ 20

4. ECOG PS 0-2

5. Documented progressive disease after one or more conventional systemic chemotherapy

6. At least one measurable disease by RECIST v1.1

7. Adequate organ function for treatment as follows:

• Absolute neutrophil count > 1.5 x 109/L
• Platelets >100 x 109/L
• Serum creatinine ≤ 2.0 x ULN (upper limit of normal)
• Serum bilirubin ≤ 1.5 x ULN
• AST and ALT ≤ 2.5 x ULN (without liver metastasis), ≤ 5.0 x ULN (with liver metastasis)

8. Life expectancy ≥ 12 weeks at day 1

Exclusion Criteria

1. Previous treatment with sunitinib or other VEGF-TKIs

2. Any major operation or irradiation within 4 weeks of baseline disease assessment

3. Any clinically significant gastrointestinal abnormalities which may impair intake or absorption of the study drug

4. CNS metastasis with continuous corticosteroid use within 4 weeks of baseline disease assessment (Asymptomatic CNS metastasis patients can be enrolled)

5. Patients with uncontrolled or significant cardiovascular disease (AMI within 12 months, Unstable angina within 6 months, NYHA Class III, IV Congestive heart failure or left ventricular ejection fraction below local institutional lower limit of normal or below 45%, Congenital long QT syndrome, Any significant ventricular arrhythmia, Any uncontrolled second or third degree heart block, Uncontrolled hypertension)

6. Concomitant malignancy (except adequately treated basal cell cancer of skin or cervical cancer in situ)

7. Female patients who are pregnant, breast-feeding or male or female patients of reproductive potential who are not employing an effective method of birth control

8. Other severe acute or chronic medical condition or laboratory abnormality that may increase the risk associated with trial participation or investigational product administration or may interfere with the interpretation of trial results and, in the judgment of the investigator, would make the patient inappropriate for entry into this trial. (including active bleeding, untreated DVT or thromboembolism)

• Minimum Eligible Age: 20 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

SMG-SNU Boramae Medical Center

OTHER

Sponsor Role: collaborator

Seoul National University Hospital

OTHER

Sponsor Role: lead

Responsible Party

Jong-Seok Lee

Professor of Internal Medicine

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Jong Seok Lee, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Seoul National University Bundang Hospital

Locations

Seoul National University Bundang Hospital

Seongnam, , South Korea

Countries

South Korea

Related Links

https://doi.org/10.1016/j.jtho.2018.08.297

Oral Presentation at WCLC 2018 (OA11.05 )

Other Identifiers

SNUBH-15-01

Identifier Type: -

Identifier Source: org_study_id