Retlirafusp Alfa Combined With Chemotherapy or Fuzuloparib for Triple-Negative Breast Cancer
Retlirafusp Alfa Combined With Chemotherapy or Fuzuloparib for Triple-Negative Breast Cancer: An Exploratory Clinical Study
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Fase 2
Kontakter og lokationer
Studiekontakt
Studiekontakt
- Navn: Tong Liu, M.D.
- Telefonnummer: +8615945953777
- E-mail: liutong@hrbmu.edu.cn
Studiesteder
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Heilongjiang
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Harbin, Heilongjiang, Kina, 150081
- Harbin Medical University Cancer Hospital
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Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Age ≥18 years, female;
- 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 -);
- At least one measurable lesion per RECIST version 1.1 criteria;
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;
- Life expectancy ≥3 months;
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-1;
- Available tissue sample for testing, and gBRCA1/2 mutation status must be determined prior to treatment;
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;
- 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;
- Willing to participate, capable of providing signed informed consent, and compliant with study procedures.
Exclusion Criteria:
- Concurrently receiving anti-tumor therapy in another clinical trial;
- Received other anti-tumor therapy within 4 weeks prior to the first dose of study drug;
- Prior treatment with tumor immunotherapy (including but not limited to PD-1, PD-L1, CTLA-4 inhibitors, etc.) or TGF-β inhibitors;
- Prior treatment with PARP inhibitors (except for patients who completed PARP inhibitor therapy for ovarian cancer ≥5 years ago with no recurrence or metastasis);
- Untreated active brain metastases or leptomeningeal metastases;
- Underwent major surgery unrelated to breast cancer within 4 weeks prior to enrollment, or have not fully recovered from such surgery;
- 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;
- 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);
- Congenital or acquired immunodeficiency (e.g., HIV-infected patients);
- Received live vaccine within 4 weeks prior to study drug administration or likely to receive such vaccine during the study period;
- Known hypersensitivity to any component of the study drugs in this protocol;
- 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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
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Eksperimentel: Advanced cohort: gBRCA1/2 wild-type
Retlirafusp alfa + nab-paclitaxel
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Retlirafusp alfa+Nab-paclitaxel
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Eksperimentel: Advanced cohort: gBRCA1/2 pathogenic or likely pathogenic mutation
Retlirafusp alfa + fluzoparib
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Retlirafusp alfa+Fluzoparib
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Eksperimentel: Early neoadjuvant cohort: gBRCA1/2 wild-type
Retlirafusp alfa+TP-AC
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Retlirafusp alfa+TP-AC
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Eksperimentel: Early neoadjuvant cohort: gBRCA1/2 pathogenic or likely pathogenic mutation
Retlirafusp alfa+ Fluzoparib
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Retlirafusp alfa+Fluzoparib
|
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Late-Stage Cohort-Objective Response Rate
Tidsramme: 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.
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Assessed every 6 weeks (every 2 cycles) during treatment until disease progression, death, or loss to follow-up. Analysis cutoff at 6 months.
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Neoadjuvant Cohort-tpCR (ypT0/is ypN0)
Tidsramme: Surgery performed 2-6 weeks after completing 8 cycles (≈24 weeks) of neoadjuvant therapy; pathological assessment post-surgery. Analysis cutoff at 6 months.
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Pathologic complete response with no residual invasive carcinoma in breast and ipsilateral lymph nodes after neoadjuvant therapy and surgery.
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Surgery performed 2-6 weeks after completing 8 cycles (≈24 weeks) of neoadjuvant therapy; pathological assessment post-surgery. Analysis cutoff at 6 months.
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Late-Stage Cohort-Disease Control Rate
Tidsramme: 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.
|
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Late-Stage Cohort-Clinical Benefit Rate
Tidsramme: 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
Tidsramme: Assessed every 3 months during treatment and follow-up until disease progression, death, or start of subsequent anticancer therapy. Analysis cutoff at 36 months.
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Time from treatment initiation to first radiographic disease progression or death from any cause.
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Assessed every 3 months during treatment and follow-up until disease progression, death, or start of subsequent anticancer therapy. Analysis cutoff at 36 months.
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Late-Stage Cohort-Overall Survival
Tidsramme: Follow-up every 3 months via clinic visit or telephone call after treatment completion until death or study end. Analysis cutoff at 36 months.
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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.
|
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Neoadjuvant Cohort-bpCR (ypT0/is)
Tidsramme: 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
Tidsramme: 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.
|
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Neoadjuvant Cohort-Event-Free Survival
Tidsramme: 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.
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Follow-up every 3 months from treatment start until event or study end. Analysis cutoff at 36 months.
|
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Neoadjuvant Cohort-Disease-Free Survival
Tidsramme: Follow-up every 3 months from surgery until recurrence, death, or study end. Analysis cutoff at 36 months.
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Time from surgery to first postoperative recurrence or death from any cause.
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Follow-up every 3 months from surgery until recurrence, death, or study end. Analysis cutoff at 36 months.
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Neoadjuvant Cohort-Distant Disease-Free Survival
Tidsramme: Follow-up every 3 months from surgery until distant metastasis, death, or study end. Analysis cutoff at 36 months.
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Time from surgery to first distant metastasis or death from any cause.
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Follow-up every 3 months from surgery until distant metastasis, death, or study end. Analysis cutoff at 36 months.
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Adverse Event (AE) Incidence
Tidsramme: 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.
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Incidence, severity, and drug-relatedness of AEs and SAEs, graded per NCI-CTCAE v6.0.
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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.
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Biomarker Exploration
Tidsramme: 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.
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Collection of tumor tissue and peripheral blood samples to analyze potential biomarkers associated with efficacy, resistance, and safety.
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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.
|
Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- MA-BC-II-146
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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