Testing a new treatment for advanced thymic tumors

A Phase II Parallel Arm Study of SACITUZUMAB GOVITECAN-HZIY in Patients With Advanced Thymoma and Thymic Carcinoma

This study is testing a new drug to see if it can help adults with advanced thymic tumors who haven't had success with other treatments.

Quick facts

• Phase: Phase 2
• Study type: Interventional
• Enrollment: 18 (estimated)
• Ages: 18 Years and up
• Sex: All
• Sponsor: Georgetown University (Academic / other)
• Drugs / interventions: sacituzumab
• Locations: 4 sites (Palo Alto, California and 3 other locations)
• Trial ID: NCT06248515 on ClinicalTrials.gov

What this trial studies

This clinical trial investigates the effectiveness of sacituzumab govitecan-hziy in adult patients with advanced thymoma and thymic carcinoma who have not responded to at least one prior treatment. Participants will receive a fixed dose of the drug intravenously once a week for 21-day cycles, with ongoing monitoring through blood tests and scans. The primary goal is to determine the overall response rate in these patients, contributing valuable data to the understanding of treatment options for this rare cancer.

Who should consider this trial

Good fit: Ideal candidates are adults aged 18 and older with histologically confirmed advanced thymoma or thymic carcinoma who have experienced disease progression after prior systemic therapy.

Not a fit: Patients with early-stage thymoma or thymic carcinoma who have not undergone prior systemic therapy may not benefit from this study.

Why it matters

Potential benefit: If successful, this treatment could provide a new therapeutic option for patients with advanced thymic tumors who have limited alternatives.

How similar studies have performed: While there is limited data on sacituzumab govitecan specifically for thymic tumors, similar approaches in treating other cancers have shown promising results.

Eligibility criteria

Inclusion Criteria:

* Age \>/= 18 years at time of signing informed consent form (ICF)
* Ability to understand and the willingness to sign a written informed consent document
* Patients with histologically confirmed advanced thymoma or thymic carcinoma
* Patients who have experienced disease progression after treatment with at least one prior systemic therapy
* Measurable disease per RECIST v1.1
* Availability of pre-treatment tumor tissue (archival or fresh); If archival tissue is not available and a fresh biopsy is not considered safe and medically feasible by the Investigator, the patient may be approved for enrollment after consultation with the Principal Investigator
* Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-2
* Adequate hematologic and end-organ function, defined by the following laboratory test results, obtained within 14 days prior to initiation of study treatment:
* Absolute neutrophil count (ANC) \>/= 1.5 x 10\^9/L (1500/uL) without filgrastim support
* Platelet count \>/= 100 x 10\^9/L (100,000/uL) without transfusion
* Hemoglobin (Hgb) \>/= 80 g/L (8 g/dL). Patients may be transfused to meet this criterion.
* Aspartate aminotransferase (AST), alanine transaminase (ALT), and alkaline phosphatase (ALP) \</= 2.5 x upper limit of normal (ULN), with the following exceptions:

  * Patients with documented liver metastases: AST and ALT \</= 5 x ULN
  * Patients with documented liver or bone metastases: ALP \</= 5 x ULN Serum bilirubin \</= 1.5 x ULN with the following exception: patients with known Gilbert disease: serum bilirubin \</= 3 x ULN
* Creatinine clearance \>/= 30 mL/min (calculated using the Cockcroft-Gault formula, see Appendix 2)
* For patients not receiving therapeutic anticoagulation: INR and aPTT \</= 1.5 x ULN
* Patients with human immunodeficiency virus (HIV) on effective anti-retroviral therapy with undetectable viral load are eligible for this trial
* For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable or on suppressive therapy, if indicated. Patients with a history of hepatitis C virus (HCV) infection must have been treated. For patients with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load.
* Patients with prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial
* For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive methods, and agreement to refrain from donating eggs, as defined below:

  * Women must remain abstinent or use contraceptive methods with a failure rate of \< 1% per year during the treatment period and for 6 months after the final dose of study treatment. Women must refrain from donating eggs during this same period.
  * A woman is considered to be of childbearing potential if she is postmenarchal, has not reached a postmenopausal state (\>/= 12 continuous months of amenorrhea with no identified cause other than menopause), and has not undergone surgical sterilization (removal of ovaries and/or uterus). The definition of childbearing potential may be adapted for alignment with local guidelines or requirements.
  * Examples of contraceptive methods with a failure rate of \> 1% per year include bilateral tubal ligation, male sterilization, hormonal contraceptives that inhibit ovulation, hormone-releasing intrauterine devices, and copper intrauterine devices.
  * The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not adequate methods of contraception.
* For men: agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive measures, and agreement to refrain from donating sperm, as defined below:

  * With a female partner of childbearing potential who is not pregnant, men who are not surgically sterile must remain abstinent or use a condom plus an additional contraceptive method that together result in a failure rate of \< 1% per year during the treatment period and for 90 days after the final dose of sacituzumab govitecan-hziy. Men must refrain from donating sperm during this this same period.
  * With a pregnant female partner, men must remain abstinent or use a condom during the treatment period and 90 days after the final dose of sacituzumab govitecan-hziy to avoid potential exposure to the embryo.
  * The reliability of sexual abstinence should be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the patient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or postovulation methods) and withdrawal are not adequate methods of contraception.

Exclusion Criteria:

* Any other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding that, in the view of the investigator, contraindicates the use of an investigational drug, may affect the interpretation of the results, or may render the patient at high risk from treatment complications.
* Pregnancy or breastfeeding, or intention of becoming pregnant during study treatment or within 6 months after the final dose of study treatment.
* Symptomatic brain metastasis requiring corticosteroids. Patients with treated brain metastases are eligible.
* No concurrent therapy with approved or investigational anticancer therapeutics

Where this trial is running

Palo Alto, California and 3 other locations

• Stanford Cancer Institute — Palo Alto, California, United States (Recruiting)
• Lombardi Comprehensive Cancer Center, Georgetown University — Washington D.C., District of Columbia, United States (Recruiting)
• University of Chicago Medical Center — Chicago, Illinois, United States (Recruiting)
• John Theurer Cancer Center at Hackensack University Medical Center — Hackensack, New Jersey, United States (Recruiting)

Study contacts

• Principal investigator: Chul Kim, MD — [e-mail]
• Study coordinator: Chul Kim, MD

Conditions Thymoma; Thymic Carcinoma