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Pembrolizumab + Paclitaxel +/- Bevacizumab for Triple-negative Breast Cancer (PRELUDE)

Y

Yukinori Ozaki

Status and phase

Enrolling
Phase 2

Conditions

Recurrent Triple-Negative Breast Cancer

Treatments

Drug: Bevacizumab
Drug: Pembrolizumab
Drug: Paclitaxel

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT06976944
WJOG16522B
jRCT2031250076 (Registry Identifier)

Details and patient eligibility

About

  • 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.

Enrollment

44 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Male/female participants who are 18 years of age or older on the day of signing informed consent with histologically or cytologically confirmed diagnosis of invasive breast cancer will be enrolled in this study.
  2. Participants have been confirmed to be ER negative, HER2 negative according to the latest ASCO/CAP criteria. However, it does not matter whether the result is positive or negative for PgR.
  3. Participants have been confirmed to be PD-L1 positive in each site's evaluation using biopsy specimen or surgical specimen.
  4. Participants who have not undergone chemotherapy for recurrent breast cancer. However, prior treatment of Olaparib for metastatic recurrence or unresectable advanced cancer in participants with BRCA gene pathogenic variant is allowed.
  5. 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.
  6. Have an Eastern Cooperative Oncology Group performance status of 0 to 1.

Exclusion criteria

  1. Participants with progressive disease on RECIST or clinically diagnosed during preoperative ICI and chemotherapy.
  2. Known additional malignancy that is progressing or has required active treatment within the past 3 years prior to enrollment.
  3. Has known active CNS metastases and/or carcinomatous meningitis.
  4. Has a history of (non-infectious) pneumonitis/interstitial lung disease that required steroids or has current pneumonitis/interstitial lung disease.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

44 participants in 2 patient groups

Pembrolizumab + paclitaxel + bevacizumab
Experimental group
Treatment:
Drug: Bevacizumab
Drug: Paclitaxel
Drug: Pembrolizumab
Pembrolizumab + paclitaxel
Active Comparator group
Treatment:
Drug: Paclitaxel
Drug: Pembrolizumab

Trial contacts and locations

15

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Central trial contact

Yukinori Ozaki; Kazuki Nozawa

Data sourced from clinicaltrials.gov

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