Safety and Efficacy Analysis of an Antibody Associated With a Chemotherapy for Patients With a Triple Negative Metastatic Breast Cancer

Launched by UNICANCER · Sep 20, 2022

Keywords

ClinConnect Summary

This clinical trial, called ISIdE, is studying a new treatment for people with triple-negative metastatic breast cancer, which is a type of breast cancer that does not respond to some common treatments. The trial is specifically looking at the effectiveness of a drug called Sacituzumab Govitecan (SG) in patients whose cancer has progressed despite previous chemotherapy or within six months after finishing other treatments. Researchers want to find out how well this drug works in patients who have had fewer prior treatments and hope to identify specific markers that might help predict how well a patient will respond to the drug.

To participate in this trial, patients need to be at least 18 years old, have a confirmed diagnosis of locally advanced or metastatic triple-negative breast cancer, and have measurable disease. They should also be willing to undergo multiple biopsies during the study. This trial will include 100 patients, and those chosen can expect to receive the study treatment along with regular check-ups to monitor their health. It's important to note that participants will need to meet certain health criteria and cannot be currently receiving other cancer treatments. Overall, this trial seeks to provide new hope for those battling this challenging type of cancer.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Patient must have signed a written informed consent prior to any trial specific procedures;
• • Note: When the patient is unable to write to give his written consent, a trusted person of their choice, independent from the investigator or the sponsor, can confirm in writing the patient's consent
• • 2. Male or female ≥ 18 years of age;
• • 3. Patients with pathologically documented locally advanced inoperable or metastatic triple negative breast cancer (mTNBC) whose disease has progressed on (neo)adjuvant chemotherapy+/-immunotherapy for early TNBC or within 6 months after the end of any systemic therapy, surgery or radiotherapy with curative intent, whatever comes last.
• • Note: TNBC is defined as the absence of HER2 overexpression by immunohistochemistry (IHC) defined as IHC 0, 1+, or 2+ and fluorescence in situ hybridization \[FISH\] non-amplified and estrogen receptor (ER) expression \<10% and progesterone receptor (PR) expression \<10% by local pathological assessment on the most recent tissue sample collected
• • 4. Prior exposure to a taxane
• • Note: If indicated, prior therapy with ICI for patients with PD1 positive tumor and prior treatment with PARP inhibitor for patients with gBRCAm is required
• • 5. Measurable disease, as defined by RECIST v1.1
• • 6. Patient must have accepted to perform on-treatment biopsies. If the physician considers doing the biopsy on the primary tumor site because accessibility, it can be performed only if the primary tumor site has not been previously irradiated;
• • 7. Have metastatic site easily accessible to biopsy (with exception of bone metastasis)
• • Note 1: Patients with only bone metastasis will be eligible if the primary tumor is accessible for biopsy at inclusion
• • Note 2: If the patient has a single measurable lesion and it is the only one that can be biopsied, the patient cannot be included because the disease is no longer measurable according to RECIST v1.1
• • 8. Eastern Cooperative Oncology Group (ECOG) performance status ≤2;
• • 9. Life expectancy ≥12 weeks;
• • 10. Adequate haematologic and organ function
• • 11. Negative hepatitis B surface antigen (HBsAg) test at screening (patients with a negative HBsAg test and a positive total hepatitis B core antibody (HBcAb) test at screening are eligible), negative hepatitis C virus (HCV) antibody test at screening, or positive HCV antibody test followed by a negative HCV RNA test at screening;
• • 12. Evidence of post-menopausal status or negative pregnancy urinary test within 72 hours or serum pregnancy test within 14 days before study treatment and confirmed prior to treatment on Cycle 1 Day 1 for female pre-menopausal patients;
• • 13. Woman of childbearing potential and male patient must agree to use adequate contraception for the duration of trial participation and up to 6 months after completing treatment for women and up to 3 months for men;
• • 14. Patient affiliated to a social security system (or equivalent);
• • 15. Patient is willing and able to comply with the protocol for the duration of the trial including undergoing treatment and scheduled visits, and examinations including follow-up;
• Exclusion Criteria:
• • 1. Participation in another therapeutic trial within the 30 days prior to C1D1;
• • 2. Symptomatic, untreated, or actively progressing central nervous system (CNS) metastases or evidence of leptomeningeal disease or clinically active spinal cord compression. Patients with stable and asymptomatic brain metastases will be eligible, yet the number will be capped to 15% of the overall population;
• • 3. Previous history of cancer other than mTNBC within 5 years prior to C1D1, except of those with a negligible risk of metastasis or death (e.g., 5-year OS rate \>90%) and treated with curative intent (e.g. carcinoma in situ of the cervix, non-melanoma skin carcinoma, localized prostate cancer, ductal carcinoma in situ, or stage I uterine cancer);
• • 4. Prior treatment with topoisomerase-1 inhibitor or with ADC containing topoisomerase-1 inhibitor
• 5. Met any of the following criteria for cardiac disease:
• • 1. Myocardial infarction or unstable angina pectoris within 6 months of enrolment.
• • 2. History of serious ventricular arrhythmia (ie, ventricular tachycardia or ventricular fibrillation), high-grade atrioventricular block, or other cardiac arrhythmias requiring antiarrhythmic medications (except for atrial fibrillation that is well controlled with antiarrhythmic medication); history of QT interval prolongation.
• • 3. New York Heart Association (NYHA) Class III or greater congestive heart failure or left ventricular ejection fraction of \<40%.
• • 6. Severe uncontrolled infection requiring oral or IV antibiotics within 4 weeks prior to C1D1;
• • 7. Major surgical procedure within 4 weeks prior to C1D1;
• • 8. History of severe allergic, anaphylactic, or other hypersensitivity reactions to humanized antibodies;
• • 9. Known hypersensitivity to the study drug, its metabolites, or formulation excipient.
• • 10. Patients receiving concomitant anti-cancer treatments such as chemotherapy, immunotherapy, endocrine therapy and radiotherapy;
• • 11. Patients with unresolved toxicities from previous anticancer therapy, defined as toxicities (other than alopecia) not yet resolved according to the common terminology criteria for adverse events of the National Cancer Institute (NCI-CTCAE) v5.0 grade \>2
• • 12. Treatment with systemic corticosteroids dosed at \>20 mg prednisone or equivalent or other systemic immunosuppressive medications within 2 weeks prior to C1D1;
• • 13. Known history of testing positive for HIV or known acquired immunodeficiency syndrome if not controlled;
• • 14. Evidence of significant uncontrolled concomitant disease;
• • 15. Requirement for ongoing therapy with medications that are prohibited or to be used with caution
• • 16. Individuals with physical or psychological conditions considered not to be compatible with the trial;
• • 17. Persons deprived of their liberty or under protective custody or guardianship;
• • 18. Pregnant or breastfeeding women;
• • 19. Patients unwilling or unable to comply with the medical follow-up required by the trial because of geographic, familial, social, or psychological reasons.