Selinexor in Patients With Advanced Thymoma and Thymic Carcinoma (TET-SEL)

Morten Mau-Soerensen

Status and phase: Unknown; Phase 2

Conditions: Thymoma; Advanced Thymic Epithelial Tumour

Treatments: Drug: Selinexor

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT03466827

TET-SEL

Details and patient eligibility

About

The aim of the study is to determine the efficacy of selinexor in adults with TETs determined by overall response rate (RECIST 1.1) in two parallel cohorts of patients with advanced thymomas or thymic carcinomas. The study is an international, multicenter, open label phase II trial using Simons two stage design. The study population is adults with histologically confirmed, advanced, inoperable TETs who are progressing after treatment with least one platinum containing chemotherapy regimen.

This study is comprised of 2 similar phase II tirals, one running in EU (25 patients) and one running in US (25 patients).

There are two study arms:

Arm A: Thymoma

• Stage 1: 15 patients
• Stage 2: 10 patients

Arm B: Thymic carcinoma

• Stage 1: 15 patients
• Stage 2: 10 patients

Full description

Not provided

Enrollment: 25 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Histologically confirmed advanced TET (thymoma or thymic carcinoma)

• Inoperable per local Investigator (Masaoka Stage III or IV)

• Progression after treatment with least one platinum containing chemotherapyregimen

• Measurable disease (RECIST 1.1)

• Age ≥18 years

• ECOG PS <2

• Patients must have recovered from the toxic effects of prior therapy at the time of initiation of the study drug unless toxicity is stable.

• A 4 weeks interval from any investigational agents or cytotoxic chemotherapy to start of study is required

• Signed informed consent

• Adequate bone marrow function and organ function:

  • Hematopoietic function: total white blood cell count (WBC) ≥ 3000/mm³, absolute neutrophil count (ANC) ≥ 1500/mm³, platelet count ≥ 100,000/mm²
  • Hepatic function: bilirubin < 1.5 times the upper limit of normal (ULN), ALT < 2.5 times ULN or ALT < 5.0 times ULN in the presence of liver metastases
  • Creatinine clearance > 30 ml/min according to Cockcroft-Gault

• Patients of childbearing potential must agree to use adequate birth control during and for 3 months after participation in this study

Exclusion criteria

• No significant medical illness that in the investigator's opinion cannot be adequately controlled with appropriate therapy or would compromise the patient's ability to tolerate this therapy, including

  • Unstable cardiovascular function
  • Known active hepatitis A, B, or C infection; or known to be positive for HCV RNA or HBsAg (HBV surface antigen)
  • Markedly decreased visual acuity
  • Active infection requiring intravenous antibiotics

• Pregnancy or breast-feeding

• Symptomatic brain metastasis requiring corticosteroids

• Uncontrolled autoimmune disorders. Patients with autoimmune disorders under control on medication may be included. Patients with pure red cell aplasia may be included if haemoglobin levels are relatively stable on transfusions or medication

• Any other cancer (excluding radically operated localised squamous skin cancer) with clinical activity within the last 2 years

• Significantly diseased or obstructed gastrointestinal tract, malabsorption, uncontrolled vomiting or diarrhea or inability to swallow oral medications

• No dehydration of NCI-CTCAE grade ≥ 1

• Serious psychiatric or medical conditions that could interfere with treatment.

• No history of organ allograft

• No concurrent therapy with approved or investigational anticancer therapeutics

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)