Breast Cancer Clinical Trial
Direct Tumor Microinjection and FDG-PET in Testing Drug Sensitivity in Patients With Relapsed or Refractory Non-Hodgkin Lymphoma, Hodgkin Lymphoma, or Stage IV Breast Cancer
This pilot phase I trial studies the side effects of direct tumor microinjection and fludeoxyglucose F-18 positron emission tomography (FDG-PET) in testing drug sensitivity in patients with non-Hodgkin lymphoma, Hodgkin lymphoma, or stage IV breast cancer that has returned after a period of improvement or does not respond to treatment. Injecting tiny amounts of anti-cancer drugs directly into tumors on the skin or in lymph nodes and diagnostic procedures, such as FDG-PET, may help to show which drugs work better in treating patients with non-Hodgkin lymphoma, Hodgkin lymphoma, or breast cancer.
I. To assess the safety of in vivo in host drug sensitivity testing in patients with breast cancer and patients with lymphoma (nodal, extranodal masses, or cutaneous lesions).
I. To assess the feasibility of in vivo in host drug sensitivity testing in this patient population.
II. To identify targeted therapies with potential activity in relapsed lymphoma and metastatic breast cancer.
III. To evaluate the adverse event profile within each patient population.
I. To assess for apoptosis in response to intratumoral injection using known biomarkers (e.g., by morphology, Ki-67, caspace-3 assay as a marker of early apoptosis).
II. To evaluate intratumoral biomarkers, intratumoral cell populations, and distribution, identify potential biomarkers that correlate with response to therapy based on individual therapies.
Patients undergo FDG-PET and receive saline intralesionally on day 1. Patients also receive up to five additional injections of gemcitabine hydrochloride, romidepsin, belinostat, carfilzomib, copanlisib hydrochloride, nivolumab, trastuzumab, daratumumab, obinutuzumab, pembrolizumab, or rituximab intralesionally per investigator on day 1. Beginning 5 days later, patients with nodal/extranodal mass undergo restaging FDG-PET and biopsy (if clinically feasible). Within 3-7 days, patients with cutaneous disease undergo restaging photography and biopsy.
After completion of study treatment, patients are followed up at 3 months.
Age >= 18 years
Histologically proven of relapsed or refractory
Non-Hodgkin lymphoma (NHL) or Hodgkin lymphoma (HL) nodal or extranodal mass OR
Cutaneous T-cell lymphoma (CTCL) including mycosis fungoides (MF), as well as transformed MF OR
Breast adenocarcinoma with nodal or cutaneous metastases (stage 4)
NOTE: Patients must be refractory to or intolerant of existing therapy(ies) known to provide clinical benefit for their condition
NOTE: The patient must not be a candidate for any curative therapy or any known life-prolonging therapy
Cohort I: For nodal/extranodal mass, presence of lesions that are amenable for injections as determined by interventional radiology
NOTE: Nodal or extranodal mass must be palpable and easily accessible; masses such as mediastinum, retroperitoneum, within solid organs, spinal sites, central nervous system (CNS) sites, etc., are NOT allowed
For nodal or extranodal disease (lymphoma or breast): must have at least 2 lesions that are >= 20 mm (2.0 cm) in the longest diameter by physical exam and/or on cross-sectional imaging and measurable in two perpendicular dimensions per computed tomography PET-computed tomography (CT); For Cohort I, the lesions must be amenable to intralesional injections as determined by interventional radiology (including tumors that can be safely accessed using imaging guidance and treated with minimal risk to adjacent structures)
For cutaneous lesions (lymphoma or breast): at least two visible, non-infected skin lesions that are greater than 1 cm and are amenable to intralesional injection as determined by investigator
Candidate for further therapy and able to wait 7 days prior to start of next systemic therapy
Absolute neutrophil count (ANC) >= 1000/mm^3 (obtained =< 14 days prior to registration)
Platelet count >= 50,000/mm^3 (obtained =< 14 days prior to registration)
International normalized ratio (INR)/prothrombin time (PT) =< 1.5 (obtained =< 14 days prior to registration)
Negative serum or urine pregnancy test done =< 7 days prior to registration, for persons of childbearing potential only
Provide written informed consent
Willing to return to enrolling institution for follow-up
Willing to provide tissue samples for correlative research purposes
Any of the following:
Persons of childbearing potential who are unwilling to employ adequate contraception
Co-morbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens
Systemic corticosteroids between pre-PET and post-PET evaluation and biopsy
Prohibited treatments and or therapies
Autologous stem cell transplant (ASCT) =< 12 weeks prior to registration
Prior chemotherapy =< 2 weeks prior to registration
Prior treatment with nitrosureas =< 4 weeks prior to registration
Therapeutic anticancer antibodies =< 2 weeks prior to registration
Radio- or toxin immunoconjugates =< 4 weeks prior to registration
Radiation therapy to the injected area =< 2 weeks prior to registration
Major surgery =< 2 weeks prior to registration
Receiving any other investigational agent which would be considered as a treatment for the primary neoplasm
Requires anticoagulation that cannot be discontinued prior to biopsy
Note: Exception if able to hold antiplatelet agents 7 days prior to the injections and biopsy
NOTE: Low molecular weight heparin (LMWH) will be allowed for bridging if on warfarin
NOTE: Heparin for line patency without detectable lab abnormalities for coagulation will be allowed
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There is 1 Location for this study
Rochester Minnesota, 55905, United States
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