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

4 agosto 2026 aggiornato da: 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.

Panoramica dello studio

Descrizione dettagliata

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.

Tipo di studio

Interventistico

Iscrizione (Stimato)

120

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

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

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Non randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Advanced cohort: gBRCA1/2 wild-type
Retlirafusp alfa + nab-paclitaxel
Retlirafusp alfa+Nab-paclitaxel
Sperimentale: Advanced cohort: gBRCA1/2 pathogenic or likely pathogenic mutation
Retlirafusp alfa + fluzoparib
Retlirafusp alfa+Fluzoparib
Sperimentale: Early neoadjuvant cohort: gBRCA1/2 wild-type
Retlirafusp alfa+TP-AC
Retlirafusp alfa+TP-AC
Sperimentale: Early neoadjuvant cohort: gBRCA1/2 pathogenic or likely pathogenic mutation
Retlirafusp alfa+ Fluzoparib
Retlirafusp alfa+Fluzoparib

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Late-Stage Cohort-Objective Response Rate
Lasso di tempo: 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)
Lasso di tempo: 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.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Late-Stage Cohort-Disease Control Rate
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

30 luglio 2026

Completamento primario (Stimato)

30 luglio 2028

Completamento dello studio (Stimato)

30 luglio 2029

Date di iscrizione allo studio

Primo inviato

4 agosto 2026

Primo inviato che soddisfa i criteri di controllo qualità

4 agosto 2026

Primo Inserito (Effettivo)

7 agosto 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

7 agosto 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

4 agosto 2026

Ultimo verificato

1 agosto 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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