Neoadjuvant Pembrolizumab, Carboplatin and Paclitaxel in Triple-negative Breast Cancer

Launched by TEL AVIV MEDICAL CENTER · May 6, 2024

Keywords

ClinConnect Summary

This clinical trial is studying a new treatment approach for patients with early-stage triple-negative breast cancer, which is a type of breast cancer that doesn’t have certain receptors that are typically targeted in treatment. The trial will assess how well a combination of medications, including pembrolizumab (an immunotherapy), carboplatin, and paclitaxel (chemotherapy drugs), helps patients achieve a complete response, meaning no signs of cancer are left after treatment. This study is currently not recruiting participants, but it aims to include men and women aged 18 and older with specific criteria, such as having a confirmed diagnosis of stage I or II triple-negative breast cancer and a tumor larger than 1 cm.

Eligible participants can expect to receive these medications in a sequence, starting with pembrolizumab followed by the combination therapy. They will need to provide some tissue samples for testing and agree to use contraception during the study if applicable. It’s important to note that participants should not have certain health conditions or previous treatments that could affect their response to the study drugs. Overall, this trial is an opportunity for individuals with this type of breast cancer to contribute to research that may lead to better treatment options in the future.

Gender

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Eligibility criteria

• Inclusion Criteria:
• • 1. Male/female participants who are at least 18 years of age on the day of signing informed consent with a histologically confirmed diagnosis of stage I or II TNBC.
• • 2. Tumor size of above 1 cm.
• • 3. The patient is willing to provide tissue from newly obtained core biopsies.
• 4. Male participants:
• • A male participant must agree to use contraception as detailed in Appendix 3 of this protocol during the treatment period and for at least 200 days after the last dose of study treatment and refrain from donating sperm during this period.
• 5. Female participants:
• A female participant is eligible to participate if she is not pregnant, not breastfeeding, and at least one of the following conditions applies:
• • 1. Not a woman of childbearing potential (WOCBP). OR
• • 2. A WOCBP who agrees to follow the contraceptive during the treatment period and for at least 180 days after the last dose of chemotherapy.
• • 6. The participant (or legally acceptable representative if applicable) provides written informed consent for the trial.
• • 7. Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1. Evaluation of ECOG is to be performed within 7 days before the first dose of study intervention.
• • 8. Have adequate organ function as defined in the following table (Table 4). Specimens must be collected within 10 days before the start of the study intervention.
• • 9. Criteria for known Hepatitis B and C positive subjects
• Hepatitis B (HBV) and C (HCV) screening tests are not required unless:
• • Known history of HBV or HCV infection
• • As mandated by the local health authority
• 10.1 Hepatitis B positive subjects:
• • Participants who are HBsAg positive are eligible if they have received HBV antiviral therapy for at least 4 weeks and have an undetectable HBV viral load before randomization.
• • Participants should remain on anti-viral therapy throughout the study intervention and follow local guidelines for HBV anti-viral therapy post-completion of the study intervention.
• • 10.2 Participants with a history of HCV infection are eligible if the HCV viral load is undetectable at screening.
• • • Participants must have completed curative anti-viral therapy at least 4 weeks before randomization.
• Exclusion Criteria:
• • 1. A WOCBP who has a positive urine pregnancy test within 72 hours prior of the first treatment dose (. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.
• • 2. Has received prior therapy with an anti-Programmed cell death-ligand-1 (PD-L1), anti-PD-1, or anti-PD L2 agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (eg, cytotoxic T-lymphocyte associated protein 4 (CTLA-4), OX 40, CD137).
• • 3. Has received prior systemic anti-cancer therapy, including investigational agents, within 24 months of screening.
• • 4. Has received prior radiotherapy within 24 months of screening.
• • 5. Has received a live vaccine or live-attenuated vaccine within 30 days before the first dose of study intervention. Administration of killed vaccines is allowed.
• • Note: please refer to Section 5.5.2 for information on coronavirus disease 2019 (COVID-19) vaccines
• • 6. Has received an investigational agent or has used an investigational device within 4 weeks before study intervention administration.
• • 7. Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy (in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of immunosuppressive therapy within 7 days before the first dose of the study drug.
• • 8. Known additional malignancy that is progressing or has required active treatment within the past 3 years. Note: Participants with basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or carcinoma in situ, excluding carcinoma in situ of the bladder, that have undergone potentially curative therapy are not excluded.
• • 9. Has severe hypersensitivity (≥Grade 3) to pembrolizumab and/or any of its excipients.
• • 10. Has active autoimmune disease that has required systemic treatment in the past 2 years except for replacement therapy (eg., thyroxine, insulin, or physiologic corticosteroid).
• • 11. Has a history of (non-infectious) pneumonitis/interstitial lung disease that required steroids or has current pneumonitis/interstitial lung disease.
• • 12. Has an active infection requiring systemic therapy.
• • 13. Has a known history of Human Immunodeficiency Virus (HIV) infection. Note: No HIV testing is required unless mandated by local health authorities.
• • 14. Concurrent active Hepatitis B (defined as HBsAg positive and/or detectable HBV DNA) and Hepatitis C virus (defined as anti-HCV Ab positive and detectable HCV RNA) infection.
• Note: Hepatitis B and C screening tests are not required unless:
• • Known history of HBV and HCV infection
• • As mandated by the local health authority
• • 15. Has not adequately recovered from major surgery or has ongoing surgical complications.
• • 16. Has a history or current evidence of any condition, therapy, laboratory abnormality, or other circumstance that might confound the results of the study, interfere with the participant's participation for the full duration of the study, such that it is not in the best interest of the participant to participate, in the opinion of the treating investigator.
• • 17. Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
• • 18. Is pregnant or breastfeeding or expecting to conceive or father children within the projected duration of the study, starting with the screening visit through 120 days after the last dose of trial treatment or 180 after the last dose of chemotherapy.
• • 19. Has had an allogeneic tissue/solid organ transplant.