Triple Negative Breast Cancer Clinical Trial
Official title:
Patient-derived Xenograft (PDX) Modeling of Treatment Response for Triple Negative Breast Cancer
This study will determine if patient-derived tumor xenograft (PDX) mouse models can serve as a reliable model for treatment response for individual patients with triple negative breast cancer. The collection of patient tumor tissue will also provide insight into the mechanisms of therapeutic resistance for those individuals. Ultimately, this study will enhance our understanding of the genomic basis for treatment response for triple negative cancer on an individual basis, while having the potential to suggest new therapeutic options for high-risk triple negative breast cancer patients with residual disease post neoadjuvant.
Triple negative breast cancer (TNBC) represents an aggressive, genomically heterogeneous,
subtype of breast cancer with limited therapeutic options. Many patients with TNBC receive
standard neoadjuvant chemotherapy (NAC) pre-operatively; response is directly correlated with
long-term outcome. Patients with residual disease after NAC are at higher risk for recurrent
or metastatic disease, but additional adjuvant therapies are not currently part of standard
care. Personalized treatment for patients with TNBC requires an improved understanding of the
genomic landscape of individual TN breast tumors, as well as improved predictive models of
response to specific therapeutic agents. This pilot study will determine if patient-derived
tumor xenograft (PDX) mouse models can serve as a reliable model for treatment response for
individual patients with TNBC. The tumor tissue collected (paired pre-and post NAC) will also
provide insight into mechanisms of therapeutic resistance for individual patients. This study
will enhance our understanding of the genomic basis for treatment response for TNBC on an
individual patient basis, and lead to potential new therapeutic options for high-risk TNBC
patients with post-NAC residual disease.
Objectives:
1. To collect and bank tissue specimens from patients with operable triple negative breast
cancer at: a) at time of diagnosis, prior to the start of neoadjuvant therapy and b) at
time of definitive surgery, after the completion of neoadjuvant therapy.
2. To collect and bank tissue specimen for patients with advanced metastatic triple
negative disease prior to start of any line therapy for metastatic disease.
3. To create patient-derived xenograft (PDX) mouse models utilizing specimens collected
pre- and post- neoadjuvant treatment
4. To determine if response of PDX tumors to cytotoxic agents in the Champions Oncology
Tumor GraftTM (COTG) assay correlates with responses observed in patients.
5. To perform genomic analyses of patient tumor specimens collected pre- and post
neoadjuvant treatment to study mechanisms of drug resistance
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05174832 -
Induction of Cisplatin/Nab-paclitaxel/Pembrolizumab Followed by Olaparib/Pembrolizumab Maintenance in mTNBC Patients
|
Phase 2 | |
Active, not recruiting |
NCT03667716 -
COM701 (an Inhibitor of PVRIG) in Subjects With Advanced Solid Tumors.
|
Phase 1 | |
Withdrawn |
NCT03634150 -
Safety and Efficacy of IV Nerofeā¢ Followed by Doxorubicin, In Metastatic Ovarian Cancer and Triple Negative Breast Cancer
|
Phase 1/Phase 2 | |
Recruiting |
NCT03348098 -
Clinical Study of Neoadjuvant Therapy With Apatinib and Paclitaxel in Local Advanced Triple-negative Breast Cancer
|
Phase 2 | |
Completed |
NCT04032080 -
LY3023414 and Prexasertib in Metastatic Triple-negative Breast Cancer
|
Phase 2 | |
Active, not recruiting |
NCT03170960 -
Study of Cabozantinib in Combination With Atezolizumab to Subjects With Locally Advanced or Metastatic Solid Tumors
|
Phase 1/Phase 2 | |
Withdrawn |
NCT02427581 -
Safety and Immunogenicity of a Personalized Synthetic Long Peptide Breast Cancer Vaccine Strategy in Patients With Persistent Triple-Negative Breast Cancer Following Neoadjuvant Chemotherapy
|
Phase 1 | |
Recruiting |
NCT03165487 -
Comparison of the Breast Tumor Microenvironment
|
||
Completed |
NCT02225470 -
Eribulin Versus Vinorelbine in Subjects With Locally Recurrent or Metastatic Breast Cancer Previously Treated With Anthracyclines and Taxanes
|
Phase 3 | |
Recruiting |
NCT04452370 -
Oral Etoposide Combined With Anlotinib in Advanced Triple Negative Breast Cancer
|
Phase 2 | |
Terminated |
NCT04123704 -
Sitravatinib in Metastatic Breast Cancer
|
Phase 2 | |
Recruiting |
NCT04758780 -
Imaging Performance Assessment of 89Zirconium-labelled Girentuximab (89Zr-TLX250) PET-CT in Metastatic Triple Negative Breast Cancer Patients
|
Phase 2 | |
Withdrawn |
NCT04268693 -
Bisphenol and Phthalate Exposures in Triple Negative Breast Cancer
|
||
Withdrawn |
NCT03982173 -
Basket Trial for Combination Therapy With Durvalumab (Anti-PDL1) (MEDI4736) and Tremelimumab (Anti-CTLA4) in Patients With Metastatic Solid Tumors
|
Phase 2 | |
Not yet recruiting |
NCT02685657 -
Neoadjuvant Chemotherapy Docetaxel With or Without SELUMETINIB in Patients With Triple Negative Breast Cancer
|
Phase 2 | |
Terminated |
NCT01918306 -
GDC-0941 and Cisplatin in Treating Patients With Androgen Receptor-Negative Triple Negative Metastatic Breast Cancer
|
Phase 1/Phase 2 | |
Completed |
NCT01276899 -
Study to Identify Molecular Mechanisms of Clinical Resistance to Chemotherapy in Triple Negative Breast Cancer Patients
|
||
Completed |
NCT00998036 -
Study of Temsirolimus, Erlotinib and Cisplatin in Solid Tumors
|
Phase 1 | |
Recruiting |
NCT05309655 -
Cardiac Outcomes With Near-Complete Estrogen Deprivation
|
Early Phase 1 | |
Active, not recruiting |
NCT03267316 -
A First-in-Human Study of CAN04 in Patients With Solid Malignant Tumors
|
Phase 1/Phase 2 |