Deze pagina is automatisch vertaald en de nauwkeurigheid van de vertaling kan niet worden gegarandeerd. Raadpleeg de Engelse versie voor een brontekst.

Retlirafusp Alfa Combined With Chemotherapy or Fuzuloparib for Triple-Negative Breast Cancer

4 augustus 2026 bijgewerkt door: Tong Liu, Harbin Medical University

Retlirafusp Alfa Combined With Chemotherapy or Fuzuloparib for Triple-Negative Breast Cancer: An Exploratory Clinical Study

To investigate the efficacy and safety of Retlirafusp alfa in combination with chemotherapy or fluzoparib for early-stage and advanced triple-negative breast cancer.

Studie Overzicht

Gedetailleerde beschrijving

Triple-negative breast cancer (TNBC) is the molecular subtype with the poorest prognosis among breast cancers, characterized by high rates of early recurrence, rapid distant metastasis, and short overall survival. Due to the lack of estrogen receptor, progesterone receptor, and HER2 expression, TNBC is insensitive to endocrine therapy and targeted therapy, making chemotherapy the mainstay of systemic treatment for a long time. However, conventional chemotherapy offers limited efficacy, and treatment options become scarce after the development of drug resistance. In recent years, immune checkpoint inhibitors have shown promising prospects in TNBC, particularly in PD-L1-positive patients who may benefit from immunotherapy combined with chemotherapy; nevertheless, a substantial proportion of patients still fail to achieve durable responses. In addition, PARP inhibitors have provided a new therapeutic option for TNBC patients harboring gBRCA mutations, and they exhibit potential synergistic effects with immunotherapy. Retlirafusp alfa (SHR-1701) is a domestically developed bifunctional fusion protein targeting PD-L1 and TGF-β, which can simultaneously block the PD-1/PD-L1 pathway and neutralize TGF-β in the tumor microenvironment, thereby enhancing anti-tumor immune responses. It has demonstrated promising efficacy and manageable safety in tumor types such as gastric cancer. Based on the above background, this study aims to explore the efficacy and safety of Retlirafusp alfa combined with chemotherapy or fluzoparib in early-stage and advanced TNBC, in order to provide novel therapeutic strategies for TNBC patients.

Studietype

Ingrijpend

Inschrijving (Geschat)

120

Fase

  • Fase 2

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Locaties

    • Heilongjiang
      • Harbin, Heilongjiang, China, 150081
        • Harbin Medical University Cancer Hospital

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

Inclusion Criteria:

  1. Age ≥18 years, female;
  2. Histopathologically confirmed recurrent or metastatic triple-negative breast cancer, defined as ER-negative (IHC ER-positive percentage <1%), PR-negative (IHC PR-positive percentage <1%), and HER2-negative (IHC -/+ or IHC ++ but FISH/CISH -);
  3. At least one measurable lesion per RECIST version 1.1 criteria;
  4. Advanced cohort:

    Metastatic or unresectable locally advanced TNBC (no prior systemic therapy or completed neoadjuvant/adjuvant therapy ≥12 months); PD-L1 positive with a Combined Positive Score (CPS) ≥1;

    Neoadjuvant cohort:

    Clinical stage II (T2N0-1M0/T3N0M0) or III (T2N2-3M0/T3N1-3M0) previously untreated breast cancer patients;

  5. Life expectancy ≥3 months;
  6. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1;
  7. Available tissue sample for testing, and gBRCA1/2 mutation status must be determined prior to treatment;
  8. Adequate major organ function meeting the following criteria (no blood transfusion or use of granulocyte colony-stimulating factor or thrombopoietin within 2 weeks prior to screening):

    Hematologic: Absolute neutrophil count (ANC) ≥1.5×10⁹/L; platelet count (PLT) ≥90×10⁹/L; hemoglobin (Hb) ≥90 g/L; Biochemical: Total bilirubin (TBIL) ≤1.5× upper limit of normal (ULN); ALT and AST ≤1.5× ULN (≤3× ULN for patients with liver metastases); alkaline phosphatase ≤2.5× ULN; BUN and creatinine ≤1.5× ULN with creatinine clearance ≥50 mL/min (calculated by Cockcroft-Gault formula); Thyroid-stimulating hormone (TSH) ≤ULN (if abnormal, T3 and T4 levels should also be assessed; patients with normal T3 and T4 levels may be enrolled); Echocardiography: Left ventricular ejection fraction (LVEF) ≥50%; 18-lead electrocardiogram: Fridericia-corrected QT interval (QTcF) <480 ms for females;

  9. Women of childbearing potential must have a negative serum or urine pregnancy test within 7 days prior to enrollment and agree to use adequate contraception during the study period and for at least 4 months after the last dose of study drug;
  10. Willing to participate, capable of providing signed informed consent, and compliant with study procedures.

Exclusion Criteria:

  1. Concurrently receiving anti-tumor therapy in another clinical trial;
  2. Received other anti-tumor therapy within 4 weeks prior to the first dose of study drug;
  3. Prior treatment with tumor immunotherapy (including but not limited to PD-1, PD-L1, CTLA-4 inhibitors, etc.) or TGF-β inhibitors;
  4. Prior treatment with PARP inhibitors (except for patients who completed PARP inhibitor therapy for ovarian cancer ≥5 years ago with no recurrence or metastasis);
  5. Untreated active brain metastases or leptomeningeal metastases;
  6. Underwent major surgery unrelated to breast cancer within 4 weeks prior to enrollment, or have not fully recovered from such surgery;
  7. Presence of any active autoimmune disease or history of autoimmune disease (including but not limited to autoimmune hepatitis, interstitial pneumonia, uveitis, enteritis, hepatitis, hypophysitis, vasculitis, nephritis, hyperthyroidism, hypothyroidism); patients with vitiligo or childhood asthma that has completely resolved and does not require any intervention in adulthood may be included; patients with asthma requiring bronchodilator therapy for medical intervention are excluded;
  8. Severe cardiac disease or conditions, including but not limited to: documented history of heart failure or systolic dysfunction (LVEF <50%); uncontrolled high-risk arrhythmias, such as atrial tachycardia, resting heart rate >100 bpm, significant ventricular arrhythmias (e.g., ventricular tachycardia), or high-grade atrioventricular block (i.e., Mobitz II second-degree or third-degree atrioventricular block); angina requiring anti-anginal medication; clinically significant valvular heart disease; ECG showing transmural myocardial infarction; poorly controlled hypertension (systolic blood pressure >180 mmHg and/or diastolic blood pressure >100 mmHg);
  9. Congenital or acquired immunodeficiency (e.g., HIV-infected patients);
  10. Received live vaccine within 4 weeks prior to study drug administration or likely to receive such vaccine during the study period;
  11. Known hypersensitivity to any component of the study drugs in this protocol;
  12. Severe concomitant disease or other comorbidities that may interfere with the planned treatment, or any other condition that, in the investigator's opinion, makes the patient unsuitable for participation in this study.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Niet-gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Advanced cohort: gBRCA1/2 wild-type
Retlirafusp alfa + nab-paclitaxel
Retlirafusp alfa+Nab-paclitaxel
Experimenteel: Advanced cohort: gBRCA1/2 pathogenic or likely pathogenic mutation
Retlirafusp alfa + fluzoparib
Retlirafusp alfa+Fluzoparib
Experimenteel: Early neoadjuvant cohort: gBRCA1/2 wild-type
Retlirafusp alfa+TP-AC
Retlirafusp alfa+TP-AC
Experimenteel: Early neoadjuvant cohort: gBRCA1/2 pathogenic or likely pathogenic mutation
Retlirafusp alfa+ Fluzoparib
Retlirafusp alfa+Fluzoparib

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Late-Stage Cohort-Objective Response Rate
Tijdsspanne: Assessed every 6 weeks (every 2 cycles) during treatment until disease progression, death, or loss to follow-up. Analysis cutoff at 6 months.
Proportion of patients with best overall response of complete response (CR) or partial response (PR) from treatment initiation to disease progression.
Assessed every 6 weeks (every 2 cycles) during treatment until disease progression, death, or loss to follow-up. Analysis cutoff at 6 months.
Neoadjuvant Cohort-tpCR (ypT0/is ypN0)
Tijdsspanne: Surgery performed 2-6 weeks after completing 8 cycles (≈24 weeks) of neoadjuvant therapy; pathological assessment post-surgery. Analysis cutoff at 6 months.
Pathologic complete response with no residual invasive carcinoma in breast and ipsilateral lymph nodes after neoadjuvant therapy and surgery.
Surgery performed 2-6 weeks after completing 8 cycles (≈24 weeks) of neoadjuvant therapy; pathological assessment post-surgery. Analysis cutoff at 6 months.

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Late-Stage Cohort-Disease Control Rate
Tijdsspanne: Assessed every 6 weeks (every 2 cycles) during treatment until disease progression, death, or loss to follow-up. Analysis cutoff at 6 months.
Proportion of patients with best overall response of CR, PR, or stable disease (SD) from treatment initiation to disease progression.
Assessed every 6 weeks (every 2 cycles) during treatment until disease progression, death, or loss to follow-up. Analysis cutoff at 6 months.
Late-Stage Cohort-Clinical Benefit Rate
Tijdsspanne: Assessed until disease progression, death, or loss to follow-up. Analysis cutoff at 6 months.
Proportion of patients with confirmed CR, PR, or SD lasting ≥24 weeks.
Assessed until disease progression, death, or loss to follow-up. Analysis cutoff at 6 months.
Late-Stage Cohort-Progression-Free Survival
Tijdsspanne: Assessed every 3 months during treatment and follow-up until disease progression, death, or start of subsequent anticancer therapy. Analysis cutoff at 36 months.
Time from treatment initiation to first radiographic disease progression or death from any cause.
Assessed every 3 months during treatment and follow-up until disease progression, death, or start of subsequent anticancer therapy. Analysis cutoff at 36 months.
Late-Stage Cohort-Overall Survival
Tijdsspanne: Follow-up every 3 months via clinic visit or telephone call after treatment completion until death or study end. Analysis cutoff at 36 months.
Time from treatment initiation to death from any cause.
Follow-up every 3 months via clinic visit or telephone call after treatment completion until death or study end. Analysis cutoff at 36 months.
Neoadjuvant Cohort-bpCR (ypT0/is)
Tijdsspanne: Surgery performed 2-6 weeks after completing 8 cycles (≈24 weeks) of neoadjuvant therapy; pathological assessment post-surgery. Analysis cutoff at 6 months.
Pathologic complete response with no residual invasive carcinoma in breast (lymph node status disregarded) after neoadjuvant therapy and surgery.
Surgery performed 2-6 weeks after completing 8 cycles (≈24 weeks) of neoadjuvant therapy; pathological assessment post-surgery. Analysis cutoff at 6 months.
Neoadjuvant Cohort-Objective Response Rate
Tijdsspanne: Assessed every 6 weeks (every 2 cycles) during neoadjuvant therapy until treatment completion. Analysis cutoff at 6 months.
Proportion of patients with best overall response of CR or PR during neoadjuvant therapy.
Assessed every 6 weeks (every 2 cycles) during neoadjuvant therapy until treatment completion. Analysis cutoff at 6 months.
Neoadjuvant Cohort-Event-Free Survival
Tijdsspanne: Follow-up every 3 months from treatment start until event or study end. Analysis cutoff at 36 months.
Time from treatment initiation to first occurrence of preoperative disease progression, postoperative recurrence, or death from any cause.
Follow-up every 3 months from treatment start until event or study end. Analysis cutoff at 36 months.
Neoadjuvant Cohort-Disease-Free Survival
Tijdsspanne: Follow-up every 3 months from surgery until recurrence, death, or study end. Analysis cutoff at 36 months.
Time from surgery to first postoperative recurrence or death from any cause.
Follow-up every 3 months from surgery until recurrence, death, or study end. Analysis cutoff at 36 months.
Neoadjuvant Cohort-Distant Disease-Free Survival
Tijdsspanne: Follow-up every 3 months from surgery until distant metastasis, death, or study end. Analysis cutoff at 36 months.
Time from surgery to first distant metastasis or death from any cause.
Follow-up every 3 months from surgery until distant metastasis, death, or study end. Analysis cutoff at 36 months.
Adverse Event (AE) Incidence
Tijdsspanne: Recorded from informed consent signing through 30 days after last dose (SAEs and immune-related AEs through 90 days after last dose); maximum follow-up of 36 months.
Incidence, severity, and drug-relatedness of AEs and SAEs, graded per NCI-CTCAE v6.0.
Recorded from informed consent signing through 30 days after last dose (SAEs and immune-related AEs through 90 days after last dose); maximum follow-up of 36 months.
Biomarker Exploration
Tijdsspanne: Blood samples collected at baseline, Cycle 5 Day 1, and Cycle 8 Day 1 (21-day cycle); tumor tissue collected at baseline from archived FFPE blocks or fresh biopsy. Analysis cutoff at 6 months.
Collection of tumor tissue and peripheral blood samples to analyze potential biomarkers associated with efficacy, resistance, and safety.
Blood samples collected at baseline, Cycle 5 Day 1, and Cycle 8 Day 1 (21-day cycle); tumor tissue collected at baseline from archived FFPE blocks or fresh biopsy. Analysis cutoff at 6 months.

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

30 juli 2026

Primaire voltooiing (Geschat)

30 juli 2028

Studie voltooiing (Geschat)

30 juli 2029

Studieregistratiedata

Eerst ingediend

4 augustus 2026

Eerst ingediend dat voldeed aan de QC-criteria

4 augustus 2026

Eerst geplaatst (Werkelijk)

7 augustus 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

7 augustus 2026

Laatste update ingediend die voldeed aan QC-criteria

4 augustus 2026

Laatst geverifieerd

1 augustus 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

Abonneren