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Neoadjuvant Angiogenesis-Targeting Bispecific Chemoimmunotherapy for TNBC (NeoASPECT)

30. července 2026 aktualizováno: Priyanka Sharma, University of Kansas Medical Center

Neoadjuvant Angiogenesis-Targeting Bispecific Chemoimmunotherapy for TNBC (NeoASPECT)

This study will test the effectiveness of two standard neoadjuvant chemotherapy regimens plus an investigational drug (ivonescimab) that has dual action as both immunotherapy and therapy targeting the tumor's blood supply. This investigational drug is called ivonescimab.

Přehled studie

Detailní popis

The standard treatment for women with high-risk early-stage triple-negative breast cancer (TNBC) includes chemotherapy plus immunotherapy (chemo-immunotherapy) given before surgery, followed by surgery, with or without radiation therapy. Patients whose tumor have low immune cell infiltration have lower response to chemoimmunotherapy and higher cancer recurrence rates. On the other hand, patients whose tumors have high immune infiltration have high response to chemoimmunotherapy and low rates of cancer recurrence and thus may not need 6 months of neoadjuvant therapy with multiple drugs. To improve outcomes for TNBC patients, we need better treatment agents, as well as ways to tailor treatment to minimize side effects.

Typ studie

Intervenční

Zápis (Odhadovaný)

110

Fáze

  • Fáze 2

Kontakty a umístění

Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.

Studijní kontakt

Kritéria účasti

Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.

Kritéria způsobilosti

Věk způsobilý ke studiu

  • Dospělý
  • Starší dospělý

Přijímá zdravé dobrovolníky

Ne

Popis

Inclusion Criteria:

Ability of participant OR Legally Authorized Representative (LAR) to understand this study, and participant or LAR willingness to sign a written informed consent

18 years of age or older

Histologically confirmed cT1c-T3 N0 or cT1-T3 N1-N2 triple-negative breast cancer

  • The invasive tumor must be hormone receptor poor, defined as both estrogen receptor (ER) and progesterone receptor staining in ≤ 10% of invasive cancer cells by IHC.
  • The invasive tumor must be HER2-negative based on the current ASCO-CAP guidelines 79.
  • Subjects with bilateral synchronous triple-negative breast cancer are eligible if they meet other eligibility criteria.

No previous ipsilateral breast surgery for the current breast cancer

No previous chemotherapy, immunotherapy, targeted therapy, endocrine therapy, or radiotherapy for the current breast cancer

ECOG Performance Status 0 or 1, documented within 21 days prior to the start of study treatment (Appendix A)

Breast and axillary imaging (including MRI and either mammogram and/or ultrasound, per standard of care) within 56 days (8 weeks) prior to treatment initiation

Subjects with clinically and/or radiographically abnormal axillary or internal mammary lymph nodes should have pathologic assessment of disease status with image-guided biopsy or fine needle aspiration unless deemed medically unsafe

Co-enrollment in the PROGECT (HSC #12614) observational registry protocol

Archival breast tumor tissue has been obtained or has been requested for use, which should include either a formalin-fixed paraffin-embedded (FFPE) block, or sixteen slides (fourteen 5-micron uncharged unstained slides plus either two H&E slides or two 5-micron charged unstained slides) - from primary breast tumor only.

Neuropathy: No baseline grade 2 or above neuropathy

Not pregnant, not breastfeeding, and at least one of the following applies:

  • Not a woman of reproductive potential as defined by institutional standards and treating physician's discretion
  • A woman of reproductive potential who agrees to follow contraceptive guidelines per institutional standards during the treatment period and for at least 3 months after the last dose of ivonescimab, or until 6 months after last dose of carboplatin or doxorubicin, 2 months after last dose of docetaxel, or 12 months after last dose of cyclophosphamide (whichever is longer).

Adequate organ function, defined as follows:

Hematologic (assessed ≤ 21 days of treatment initiation):

  • Absolute neutrophil count ≥ 1,500/μL (with the exception of patients with documented Fy(a-/b-) (Duffy null) immunophenotype, in which case absolute neutrophil count ≥1,200/uL is allowed)
  • Platelets ≥ 100,000/μL
  • Leukocytes ≥ 3,000/μL
  • Hemoglobin ≥ 9.0 g/dL or ≥ 5.6 mmol/L (must be met without erythropoietin dependency and without erythrocyte transfusion within the last two weeks)

Coagulation (assessed ≤ 21 days of treatment initiation):

For patients who are not on therapeutic anti-coagulation:

  • Prothrombin time (PT) or international normalized ratio (INR) ≤ 1.5x ULN
  • Partial prothrombin time (PTT) or activated partial prothrombin time (aPTT) ≤ 1.5x ULN (unless abnormalities are unrelated to coagulopathy). Patients receiving therapeutic anti-coagulation should be on a stable dose.

Renal (assessed ≤ 21 days of treatment initiation):

  • Creatinine ≤ 1.5 mg/dL and/or creatinine clearance ≥ 60 mL/min
  • Urine protein test <2+ or 24-hour urine protein quantification <1.0 g

Hepatic (assessed ≤ 21 days of treatment initiation):

  • Total bilirubin ≤ 1.5x ULN
  • AST(SGOT) and ALT(SPGT) ≤ 2x ULN
  • Serum albumin ≥ 3.0 g/dL

Cardiac (assessed ≤ 56 days of treatment initiation):

  • Subjects with heart failure are not eligible, nor are patients with myocardial infarction, unstable angina pectoris, an arterial thrombotic event, stroke, or transient ischemic attack within the past 12 months, uncontrolled hypertension (systolic BP > 150 mmHg, diastolic BP > 100 mmHg), uncontrolled or symptomatic arrythmia, or greater than grade 2 peripheral vascular disease
  • LVEF ≥ 50% by echocardiogram or MUGA scan, per standard of care

Exclusion Criteria:

Current or anticipated use of other investigational agents while participating in this study

Clinically or radiographically detected metastatic disease

Inflammatory breast cancer

Prior or concurrent malignancy whose natural history or treatment (in the opinion of the treating physician) has the potential to interfere with the safety or efficacy assessment of the treatment regimen.

- Note: Patients with squamous cell or basal cell carcinoma of the skin, ductal carcinoma in situ (DCIS) of the breast, or carcinoma in situ (CIS) of the uterine cervix who have undergone definitive therapy are not excluded from participation

History of allergic reactions attributed to carboplatin, docetaxel, doxorubicin, or cyclophosphamide

History of severe (≥ grade 3) hypersensitivity to ivonescimab or any of its excipients, or to any other monoclonal antibody

Prior treatment with a VEGF inhibitor or with an anti-PD-1, anti-PD-L1, anti-PD-L2 inhibitor or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (e.g., CTLA4, OX40, CD137)

History of bleeding tendencies or coagulopathy and/or clinically significant bleeding symptoms or risk within 4 weeks prior to starting study treatment, including but not limited to:

  • Hemoptysis (defined as coughing up ≥ 0.5 teaspoon of fresh blood or small blood clots). Note: Transient hemoptysis associated with diagnostic bronchoscopy is allowed.
  • Nasal bleeding /epistaxis (bloody nasal discharge is allowed)
  • Current use of prophylactic or full-dose anticoagulants or anti-platelet agents for therapeutic purposes that is not stable prior to starting study treatment. The use of full-dose anticoagulants is permitted as long as the international normalized ratio (INR) or activated partial thromboplastin time (aPTT) is within therapeutic limits according to institutional guidelines.

Poorly controlled hypertension with repeated systolic blood pressure ≥ 150 mmHg or diastolic blood pressure ≥ 100 mmHg after oral antihypertensive therapy

Major surgical procedures or serious trauma within 4 weeks prior to start of study treatment, major surgical procedures planned for within 4 weeks after the first dose of study treatment, or minor local procedures within 3 days prior to start of study treatment (as determined by the investigator).

- Note: Central venous catheterization and port implantation within 3 days prior to start of study treatment are allowed.

Subject has received a live vaccine within 30 days prior to treatment initiation

  • Live vaccines include (but are not limited to) measles, mumps, rubella, varicella/zoster (chicken pox and shingles), yellow fever, rabies, Bacillus-Calmette-Guérin (BCG), typhoid.
  • Note: Seasonal injectable influenza vaccines are killed virus and are allowed

Subject is currently receiving treatment or has received treatment with an investigational agent within four weeks prior to treatment initiation, or has used an investigational device within four weeks prior to treatment initiation

Has a diagnosis of immunodeficiency or is receiving chronic steroid therapy (in doses exceeding 10 mg daily prednisone equivalent) or any other form of immunosuppressive therapy within 7 days prior to the first dose of study treatment

Active autoimmune or lung disease that has required systemic treatment (e.g., disease-modifying agents, corticosteroids in doses exceeding 10 mg daily prednisone equivalent, immunosuppressive drugs) in the past two years.

  • Note: Patients using replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid therapy) are eligible
  • Note: Intermittent use of bronchodilators, inhaled corticosteroids, topical corticosteroids, or local corticosteroid injections is permitted

History of major diseases before starting study treatment, specifically any of the following:

  • Unstable angina, myocardial infarction, congestive heart failure (New York Heart Association [NYHA] classification ≥ grade 2) or unstable vascular disease (e.g., aortic aneurysm at risk of rupture, Moyamoya disease) that required hospitalization within 12 months prior to starting study treatment, or other cardiac impairment that may affect the safety evaluation of the study drug (e.g., poorly controlled arrhythmias, myocardial ischemia)
  • History of esophageal gastric varices, severe ulcers, wounds that do not heal, abdominal fistula, intra-abdominal abscesses, or acute gastrointestinal bleeding within 6 months before starting study treatment
  • History of any grade arterial thromboembolic event, Grade 3 and above venous thromboembolic event, as specified in National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) 5.0, transient ischemic attack, cerebrovascular accident, hypertensive crisis, or hypertensive encephalopathy within 12 months prior to starting study treatment
  • Acute exacerbation of chronic obstructive pulmonary disease within 4 weeks before starting study treatment
  • History of perforation of the gastrointestinal tract and/or fistula, history of gastrointestinal obstruction (including incomplete intestinal obstruction requiring parenteral nutrition), extensive bowel resection (partial colectomy or extensive small bowel resection) within 6 months prior to starting study treatment

Currently has or has history of (within the past one year) non-infectious pneumonitis requiring steroids

Non-infectious pneumonia requiring systemic corticosteroids within the past 30 days, or current interstitial lung disease

Infection requiring systemic therapy within 2 weeks prior to starting study treatment (excluding antiviral therapy for hepatitis B or C)

Peripheral neuropathy grade 2 or higher by CTCAE version 6

Current or history of inflammatory bowel disease (e.g., Crohn's disease, ulcerative colitis)

Known history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation

Known history of human immunodeficiency virus (HIV) infection.

- Note: Patients with controlled viral load are eligible.

Active hepatitis B (defined as HBsAg reactive) or hepatitis C (detectable HCV RNA or positive for HCV antibody)

  • Note: Patients with active hepatitis B are eligible if on appropriate antiviral therapy with acceptable tolerability for 4 weeks prior to starting study treatment, with stable or declining levels of hepatitis B DNA by polymerase chain reaction testing.
  • Note: Testing for hepatitis B and C is not required unless mandated by local health authority

History or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of this study, interfere with the subject's participation for the full duration of the study, or it is not in the best interest of the subject to participate, in the opinion of the treating investigator

Pregnancy, breastfeeding or planning to breastfeed during study treatment, or expecting to conceive within the projected duration of the study, starting with the screening visit through 90 days after the last dose of trial treatment. There is a potential for congenital abnormalities and for this regimen to harm breastfeeding infants.

Subject is a female of reproductive potential per institutional guidelines and treating physician's discretion and within 24 hours of starting treatment:

  • Serum pregnancy test is positive, or
  • Urine pregnancy test is positive or cannot be confirmed as negative, and serum pregnancy test has not been done or is positive
  • Note: In the event that 24 hours have elapsed between the screening pregnancy test and the first dose of study treatment, another pregnancy test (urine or serum) must be performed and must be negative in order for subject to start receiving study medication.

Studijní plán

Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.

Jak je studie koncipována?

Detaily designu

  • Primární účel: Léčba
  • Přidělení: Nerandomizované
  • Intervenční model: Paralelní přiřazení
  • Maskování: Žádné (otevřený štítek)

Zbraně a zásahy

Skupina účastníků / Arm
Intervence / Léčba
Jiný: Low-sTILs cohort (sTILs <30%)
4 cycles of carboplatin AUC 6 plus docetaxel 75mg/m2 plus ivonescimab 20mg/kg every 21 days, followed by 4 cycles of doxorubicin + cyclophosphamide + ivonescimab 20mg/kg every 21 days.
Komerčně dostupný
Ostatní jména:
  • Paraplatin
Commercially available
Ostatní jména:
  • Taxotere
Commercially available.
Ostatní jména:
  • Adriamycin
Commercially available.
Ostatní jména:
  • Cytoxan
Ivonescimab is a bispecific antibody targeting PD-1 and VEGF. Ivonescimab will be supplied for participants by Summit Therapeutics.
Ostatní jména:
  • SMT112, AK112
Jiný: High-sTILs cohort (sTILs ≥30%)
4 cycles of carboplatin AUC 6 plus docetaxel 75mg/m2 plus ivonescimab 20mg/kg every 21 days. Patients with lack of complete imaging response (by MRI) after 4 cycles will receive two additional cycles of carboplatin AUC 6 plus docetaxel 75mg/m2 plus ivonescimab 20mg/kg every 21 days.
Komerčně dostupný
Ostatní jména:
  • Paraplatin
Commercially available
Ostatní jména:
  • Taxotere
Ivonescimab is a bispecific antibody targeting PD-1 and VEGF. Ivonescimab will be supplied for participants by Summit Therapeutics.
Ostatní jména:
  • SMT112, AK112

Co je měření studie?

Primární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Pathologic complete response (pCR) rate in the breast and axilla in the two treatment arms.
Časové okno: At time of definitive breast surgery
Determine the rates of pathologic complete response (pCR) with ivonescimab-containing neoadjuvant systemic therapy among patients with low and high stromal tumor-infiltrating lymphocytes (sTILs), as evidenced by absence of invasive disease in breast and axillary lymph nodes (ypT0/Tis ypN0) determined by histopathological examination.
At time of definitive breast surgery

Sekundární výstupní opatření

Měření výsledku
Popis opatření
Časové okno
Treatment-related adverse events
Časové okno: Start of study treatment (cycle 1 day 1) until 30 days after last dose of study treatment (90 days for serious and immune-related adverse events)
Assess toxicity of ivonescimab in combination with chemotherapy. Toxicity will be assessed according to the NCI Common Toxicity Criteria for Adverse Events (CTCAE), version 6.0.
Start of study treatment (cycle 1 day 1) until 30 days after last dose of study treatment (90 days for serious and immune-related adverse events)
Event-free survival (EFS)
Časové okno: Up to 5 years after enrollment
3- and 5-year event-free survival (defined as the time from diagnosis to first recurrence [invasive ipsilateral breast, invasive local/regional, or distant] or to breast cancer-related death)
Up to 5 years after enrollment
Overall survival (OS)
Časové okno: Up to 5 years after enrollment
3- and 5-year overall survival (defined as the time from diagnosis to death from any cause)
Up to 5 years after enrollment

Spolupracovníci a vyšetřovatelé

Zde najdete lidi a organizace zapojené do této studie.

Vyšetřovatelé

  • Vrchní vyšetřovatel: Priyanka Sharma, MD, The University of Kansas Cancer Center

Termíny studijních záznamů

Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.

Hlavní termíny studia

Začátek studia (Odhadovaný)

1. září 2026

Primární dokončení (Odhadovaný)

1. prosince 2032

Dokončení studie (Odhadovaný)

1. prosince 2033

Termíny zápisu do studia

První předloženo

30. července 2026

První předloženo, které splnilo kritéria kontroly kvality

30. července 2026

První zveřejněno (Aktuální)

4. srpna 2026

Aktualizace studijních záznamů

Poslední zveřejněná aktualizace (Aktuální)

4. srpna 2026

Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality

30. července 2026

Naposledy ověřeno

1. července 2026

Více informací

Termíny související s touto studií

Plán pro data jednotlivých účastníků (IPD)

Plánujete sdílet data jednotlivých účastníků (IPD)?

NE

Informace o lécích a zařízeních, studijní dokumenty

Studuje lékový produkt regulovaný americkým FDA

Ano

Studuje produkt zařízení regulovaný americkým úřadem FDA

Ne

produkt vyrobený a vyvážený z USA

Ne

Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .

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