이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

Neoadjuvant Angiogenesis-Targeting Bispecific Chemoimmunotherapy for TNBC (NeoASPECT)

2026년 7월 30일 업데이트: 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.

연구 개요

상태

아직 모집하지 않음

정황

개입 / 치료

상세 설명

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.

연구 유형

중재적

등록 (추정된)

110

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위화되지 않음
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
다른: 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.
상업적으로 사용 가능하다
다른 이름들:
  • 파라플라틴
Commercially available
다른 이름들:
  • 탁소테레
Commercially available.
다른 이름들:
  • 아드리아마이신
Commercially available.
다른 이름들:
  • 사이톡산
Ivonescimab is a bispecific antibody targeting PD-1 and VEGF. Ivonescimab will be supplied for participants by Summit Therapeutics.
다른 이름들:
  • SMT112, AK112
다른: 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.
상업적으로 사용 가능하다
다른 이름들:
  • 파라플라틴
Commercially available
다른 이름들:
  • 탁소테레
Ivonescimab is a bispecific antibody targeting PD-1 and VEGF. Ivonescimab will be supplied for participants by Summit Therapeutics.
다른 이름들:
  • SMT112, AK112

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Pathologic complete response (pCR) rate in the breast and axilla in the two treatment arms.
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
Treatment-related adverse events
기간: 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)
기간: 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)
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

수사관

  • 수석 연구원: Priyanka Sharma, MD, The University of Kansas Cancer Center

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 9월 1일

기본 완료 (추정된)

2032년 12월 1일

연구 완료 (추정된)

2033년 12월 1일

연구 등록 날짜

최초 제출

2026년 7월 30일

QC 기준을 충족하는 최초 제출

2026년 7월 30일

처음 게시됨 (실제)

2026년 8월 4일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 8월 4일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 30일

마지막으로 확인됨

2026년 7월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

예

미국 FDA 규제 기기 제품 연구

아니

미국에서 제조되어 미국에서 수출되는 제품

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .