Functional Precision Oncology to Predict, Prevent, and Treat Early Metastatic Recurrence of TNBC

Breast Cancer Recurrent Clinical Trial

— TOWARDS-II  

Official title:

Towards Functional Precision Oncology to Predict, Prevent, and Treat Early Metastatic Recurrence of Triple Negative Breast Cancer

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05464082
• Other study ID #: HCI153239
• Status: Recruiting
• Phase: Phase 2
• Start date: January 6, 2023
• Est. completion date: September 30, 2027

Study information

• Verified date: February 2024
• Source: University of Utah
• Contact: Janna Espinosa
• Phone: 801-585-0571
• Email: janna.espinosa[@]hci.utah.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a prospective phase 2 study to use Functional Precision Oncology (FPO) to predict, prevent and treat early metastatic recurrence in subjects with HR-low/Her2 negative or triple negative breast cancer.

Description:

The aim of this clinical trial is to extend the findings of the investigators' first observational clinical study titled "Towards personalized medicine: patient derived breast tumor grafts as predictors of relapse and response to therapy" (TOWARDS-I). In TOWARDS-II, the investigators will develop patient derived models (PDMs), comprising patient derived xenografts (PDXs) and organoids (PDO and PDxO), from patients newly diagnosed with local or locally advanced hormone receptor-low/Her2 negative or triple negative breast cancer. The investigators will prospectively evaluate the correlation between PDX engraftment with recurrence. Using PDMs, the investigators will perform genomic studies and functional drug screens (FPO). Upon disease recurrence, the investigators will return the results to the physician with the intent to inform treatment selection.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 80
• Est. completion date: September 30, 2027
• Est. primary completion date: September 30, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Registration: Pre-tumor Collection Eligibility Participant Inclusion Criteria

• Subject aged = 18 years.

• Subject has Stage I-III disease.

• Histologically or cytologically confirmed invasive breast carcinoma that is triple negative (TNBC) or hormone receptor (HR)-low/Her2 negative

--TNBC is defined as:

• HER2 expression 0 or 1+ on immunohistochemistry (IHC) or non-amplified (defined as HER2/CEP17 ratio <2 or copy number <6) on fluorescence in situ hybridization (FISH). If HER2 expression is 2+ on IHC, negative HER2 expression must be confirmed by FISH. Pathologic diagnosis of TNBC (negative HER2 status by cytogenetics, <1% of cells stained positive for estrogen receptor (ER) by IHC, and <1% of cells stained positive for progesterone receptor (PR) by IHC).

--HR-low/Her2(-) is defined as:

• HER2 expression 0 or 1+ on IHC or non-amplified (defined as HER2/CEP17 ratio <2 or copy number <6) on fluorescence in situ hybridization (FISH). If HER2 expression is 2+ on IHC, negative HER2 expression must be confirmed by FISH.1-10% of cells stained positive for ER by IHC, and/or 1-10% of cells stained positive for PR by IHC).

• Primary tumor OR local lymph node metastasis that is = 1.5 cm. Patients with inflammatory breast cancer are eligible, regardless of tumor size. Patients with multifocal or multicentric breast cancer are eligible so long as ALL tumors biopsied per standard of care guidelines and/or investigator discretion meet receptor status criteria, and at least one tumor measures = 1.5 cm.

• Patient is considered for preoperative cytotoxic chemotherapy per standard of care or in the context of a separate, ongoing clinical trial.

• Patient has not received any prior therapy for thier breast cancer.

• Willing and capable (per treating investigator's assessment) to undergo baseline tumor material collection from the primary tumor or lymph node metastasis.

• Patient can safely undergo tumor collection:

• The tumor is reasonably accessible to tumor collection

• The tumor is amenable to tumor collection (e.g. does not abut neurovascular structures)

• If the patient receives anticoagulation, anticoagulation can be safely withheld to accommodate for tumor material acquisition

• The patient does not have a medical condition that would render tumor acquisition a high-risk procedure (e.g. tumor material acquisition from lung metastases in a patient with emphysema)

• Life expectancy of = 12 months as assessed by the treating investigator.

• ECOG Performance Status = 2.

• Evidence of post-menopausal status or negative urinary or serum pregnancy test for female pre-menopausal patients. Women will be considered post-menopausal if they have been amenorrheic for 12 months without an alternative medical cause. The following age-specific requirements apply:

• Women < 50 years of age would be considered post-menopausal if they have been amenorrheic for 12 months or more following cessation of exogenous hormonal treatments and if they have estradiol and follicle-stimulating hormone levels in the post-menopausal range for the institution or underwent surgical sterilization (bilateral oophorectomy or hysterectomy).

• Women = 50 years of age would be considered post-menopausal if they have been amenorrheic for 12 months or more following cessation of all exogenous hormonal treatments, had radiation-induced menopause with last menses >1 year ago, had chemotherapy-induced menopause with last menses >1 year ago, or underwent surgical sterilization (bilateral oophorectomy, bilateral salpingectomy or hysterectomy).

• Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines.

• No prior history of local or locally advanced hormone receptor positive (ER and/or PR expression >10% on immunohistochemistry) breast cancer, unless the following conditions are met:

• All treatment with curative intent has been completed, except adjuvant medical non-chemotherapy treatments (e.g. adjuvant endocrine therapy with any hormonal agent and/or CDK4/6 inhibitors), AND

• An interval of =6 months has elapsed between completion of these treatments and histologic diagnosis of eligible breast cancer.

Physician Inclusion Criteria

• Physician is the treating medical oncologist for a patient who meets all of the inclusion criteria and none of the exclusion criteria.

• Willing and able to answer the physician questionnaires at the protocol required time points.

• Willing and able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines.

Participant Exclusion Criteria

• Evidence of metastatic breast cancer

• ER and/or PR expression >10% on immunohistochemistry

• Her2(+) and/or Her2-amplified breast cancer. HER2 expression 3+ on IHC or amplified (defined as HER2/CEP17 ratio =2 or copy number >6) on fluorescence in situ hybridization (FISH). If HER2 expression is 2+ on IHC, reflex FISH must be performed to determine eligibility.

• Patient has bilateral breast cancer

• Patient received any anti-cancer therapy or any investigational therapy prior to study entry and collection of tumor.

--Treatment includes: neoadjuvant therapy, radiation therapy, chemotherapy, bisphosphonates for an indication other than osteopenia/osteoporosis, and/or hormonal therapy administered for the currently diagnosed primary breast cancer prior to study entry. Hormonal therapy for a prior diagnosis of a hormone receptor-positive breast cancer us allowed.

• The diagnosis of another malignancy, unless the patient is considered disease-free for =5 years before study entry. Patients are eligible if diagnosed and treated for carcinoma in situ of the cervix, melanoma in situ, colon cancer in situ, ductal carcinoma in situ, and basal and/or squamous cell carcinoma of the skin, early stage papillary thyroid cancer, and other low risk malignancies per investigator discretion.

• The subject has uncontrolled, significant intercurrent or recent illness including, but not limited to, the following conditions:

• Myocardial infarction (<6 months prior to enrollment), unstable angina, congestive heart failure (> New York Heart Association Classification Class IIB) or a serious cardiac arrhythmia requiring medication.

• Renal or liver disease that prohibits the patient from receiving at least single-agent full recommended dose chemotherapy.

• Current evidence of uncontrolled, significant intercurrent illness including, but not limited to, the following conditions:

• Cardiovascular disorders:

• Congestive heart failure New York Heart Association Class III or IV, unstable angina pectoris, serious cardiac arrhythmias.

• Stroke (including transient ischemic attack [TIA]), myocardial infarction (MI), or other ischemic events, or thromboembolic event (eg, deep venous thrombosis, pulmonary embolism) within 3 months before the first dose.

• QTc prolongation defined as a QTcF > 500 ms.

• Known congenital long QT.

• Left ventricular ejection fraction < 55%.

• Uncontrolled hypertension defined as = 160/100 as assessed from the mean of three consecutive blood pressure measurements taken over 10 minutes.

• Any other condition that would, in the Investigator's judgment, contraindicate the subject's participation in the clinical study due to safety concerns or compliance with clinical study procedures (e.g., infection/inflammation, intestinal obstruction, unable to swallow medication, [subjects may not receive the drug through a feeding tube], social/ psychological issues, etc.)

• Medical, psychiatric, cognitive, or other conditions that may compromise the subject's ability to understand the subject information, give informed consent, comply with the study protocol or complete the study.

Related Conditions & MeSH terms

• Breast Cancer Recurrent
• Breast Neoplasms
• Recurrence

Intervention

Other:
• Functional Precision Oncology
Patient derived models (PDMs), comprising patient derived xenografts (PDXs) and organoids (PDO and PDxO),

Locations

Country	Name	City	State
United States	Huntsman Cancer Institute at University of Utah	Salt Lake City	Utah

Sponsors (2)

Lead Sponsor	Collaborator
University of Utah	United States Department of Defense

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of cases where clinically actionable therapies were identified by FPO.	Assess the feasibility and utility of Functional Precision Oncology (FPO) testing to identify therapies for patients with TNBC or HR-low/HER2- breast cancer who are at high risk of early recurrence	up to 3 years
Primary	Compare the recurrence rates between patients whose tumors successfully engrafted in mice (PDX+) vs. not (PDX-)	Confirm that tumor engraftment as a PDX predicts early metastatic recurrence	Data will be assessed at 1-year from the time of definitive surgery.
Primary	Compare the recurrence rates between patients whose tumors successfully engrafted in mice (PDX+) vs. not (PDX-)	Confirm that tumor engraftment as a PDX predicts early metastatic recurrence	Data will be assessed at 3-years from the time of definitive surgery.
Secondary	Correlation between tumor engraftment (PDX+/-) and relapse-free survival, overall survival, and response to preoperative chemotherapy and treatment response as assessed on the Residual Cancer Burden scale	assess the correlation between PDX establishment and other clinical outcomes	up to 3 years
Secondary	Proportion of cases where any type of patient derived models are successfully generated and clinically actionable therapies are identified by functional precision oncology.	assess additional measures of feasibility and utility of Functional Precision Oncology	up to 3 years
Secondary	Correlation between MHCII Immune Activation Score (high vs. low and as a continuous variable) and tumor engraftment (PDX+/-) and clinical outcomes (relapse-free and overall survival).	determine the correlation between MHCII immune activation score and PDX engraftment	up to 3 years
Secondary	Correlation between methylated ctDNA measurements as assessed using the MethylPatch assay pretreatment, pre- and post surgery, with PDX engraftment data (+/-) and clinical outcomes (relapse-free and overall survival)	determine if measurement of methylated ctDNA can strengthen predictions of recurrence when combined with PDX engraftment data	up to 3 years
Secondary	frequency with which therapeutic responses in PDX, PDxO, and/or PDO align with the clinical, radiographic, and pathologic responses observed in the matched patient	determine the concordance between therapeutic responses in PDX, PDxO, and/or PDO and matched patient tumors	up to 3 years
Secondary	determine the feasibility of returning FPO results to inform the selection of 2nd line therapy after recurrence	The proportion of cases where clinically actionable therapies are identified by FPO within 12 weeks of initiating 1st line therapy after recurrence. This endpoint is restricted to the subset of patients where clinically actionable therapies were not identified prior to time of recurrence	up to 3 years
Secondary	Calculate PFS ratios of 2nd line FPO-informed: 1st line "uninformed" therapy as a preliminary measure of efficacy	assess the clinical efficacy of treatment decisions informed by FPO compared with treatment decisions not informed by FPO	up to 3 years