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OncoMatch/Clinical Trials/NCT06976944

Pembrolizumab + Paclitaxel +/- Bevacizumab for Triple-negative Breast Cancer

Is NCT06976944 recruiting? Yes, currently enrolling (Sep 2026). This Phase 2 trial studies multiple treatments including Pembrolizumab and Paclitaxel for recurrent triple-negative breast cancer.

Phase 2RecruitingYukinori OzakiNCT06976944Data as of Sep 2026Location: Japan

Treatment: Pembrolizumab · Paclitaxel · Bevacizumab* Breast cancer is histologically divided into non-invasive (approximately 10%) and invasive (approximately 90%), with invasive cancer being the target of chemotherapy. Invasive carcinoma is classified into four subtypes according to the expression levels of hormone receptor (HR) and human epidermal growth factor receptor type 2 (HER2). Among them, triple negative breast cancer accounts for 10% of invasive cancers and is the subtype with the poorest prognosis. * For triple negative breast cancer that is operable, chemotherapy with pembrolizumab is administered either preoperatively or postoperatively (perioperative period). For recurrent triple negative breast cancer , combination chemotherapy with multiple agents is the standard of care, especially in the case of PD-L1-positive patients, chemotherapy with an immune checkpoint inhibitor related to PD-1 (pembrolizumab or atezolizumab) is administered. * Although the KEYNOTE355 trial demonstrated the efficacy of pembrolizumab plus paclitaxel therapy in patients with PD-L1-positive triple negative breast cancer in postoperative relapse, this trial did not include patients who received pembrolizumab in the perioperative period. Therefore, it is not known if there is any benefit to re-administering pembrolizumab to these patients after relapse. * Bevacizumab is used as standard therapy for triple negative breast cancer in combination with paclitaxel. Bevacizumab itself is an anti-tumor agent that inhibits angiogenesis, but has also been reported to activate immunity against cancer, suggesting that it may enhance the effect of pembrolizumab. Based on the above, the investigators planned this trial to evaluate whether pembrolizumab + paclitaxel + bevacizumab therapy is more effective than pembrolizumab + paclitaxel therapy in PD-L1-positive triple negative breast cancer patients who relapse after receiving immune checkpoint inhibitors in the perioperative period.

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Pembrolizumab

Targeted therapy

Bevacizumab

Chemotherapy

Paclitaxel

Cancer type

Triple-Negative Breast Cancer

Breast Carcinoma

Biomarker criteria

Required: ESR1 wild-type (absence)

Participants have been confirmed to be ER negative

Required: HER2 (ERBB2) wild-type (absence)

Participants have been confirmed to be HER2 negative according to the latest ASCO/CAP criteria

Required: PD-L1 (CD274) expression (positive)

Participants have been confirmed to be PD-L1 positive in each site's evaluation using biopsy specimen or surgical specimen

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Max 1 prior line

Must have received: anti-PD-1/PD-L1 therapy — perioperative drug therapy for triple negative breast cancer

Participants must have recurred after treatment with an anti-PD-1/PD-L1 antibody administered as monotherapy or in combination with other ICIs or chemotherapies as a perioperative drug therapy for triple negative breast cancer

Cannot have received: paclitaxel for recurrent breast cancer (paclitaxel)

Participants with prior paclitaxel for recurrent breast cancer are excluded

Cannot have received: bevacizumab for recurrent breast cancer (bevacizumab)

Participants with prior bevacizumab for recurrent breast cancer are excluded

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT06976944 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior paclitaxel for recurrent breast cancer, bevacizumab for recurrent breast cancer disqualifies patients from enrollment.

Does this trial require ESR1?

Yes, ESR1 wild-type is a required biomarker for enrollment.

Does this trial require ERBB2?

Yes, ERBB2 wild-type is a required biomarker for enrollment.

Does this trial require CD274?

Yes, CD274 expression is a required biomarker for enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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