Leflunomide in Previously Treated Metastatic Triple Negative Cancers

Breast Neoplasms Clinical Trial

Official title:

A Phase I/II Trial of Leflunomide in Women With Previously Treated Metastatic Triple Negative Cancers

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03709446
• Other study ID #: GCO 18-1832
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: April 16, 2019
• Est. completion date: October 2026

Study information

• Verified date: May 2023
• Source: Icahn School of Medicine at Mount Sinai
• Contact: Rita Vaccaro, RN
• Phone: 212-659-5549
• Email: rita.vaccaro[@]mssm.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Triple negative breast cancer (TNBC) represents about 15% of breast cancers and is characterized by the lack of expression of estrogen receptor (ER), progesterone receptor (PR), and HER-2 non-amplification. Women with TNBC tend to be younger, African American, and BRCA-1 germline carriers. The hallmark of this subtype is early metastatic recurrences with a peak frequency 1-2 years. Prognosis for metastatic TNBC is especially poor with median survival of about 1 year as compared to about 2-4 years with other types of metastatic breast cancer. The primary objective of the phase I part of this study is to determine the safety, tolerability and maximum tolerated dose of leflunomide in women with previously treated TNBC (or ER+ , HER2-neg MBC in Phase I). The primary objective of the phase 2 part of this study is to determine the efficacy of leflunomide in patients with TNBC. Leflunomide, which will be taken daily by mouth, is an inhibitor of dihydroorotate dehydrogenase (DHODH). This proposal will test if DHODH is a novel target for a particular subset of women with metastatic TNBC.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 54
• Est. completion date: October 2026
• Est. primary completion date: October 2025
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Women with histologically confirmed HER2-negative metastatic and/or locally advanced, inoperable breast cancer on a prior biopsy performed as a component of standard of care. The biopsy site may include the primary tumor, regional lymph node, or metastatic site if accessible to biopsy.
• Age = 18.
• Prior treatment for metastatic breast cancer:
• = 3 prior chemotherapies for metastatic disease and up to 2 prior antibody drug conjugate regimens (eg, sacitizumab govitecan, trastuzumab deruxtecan). Patients with ER-positive breast cancer (ER>10%) must have had progressive disease after at least 1 prior line of CKD4/6 inhibitor, and also a PIK3CA inhibitor if known to have a somatic PIK3CA activating mutation (by tumor or ctDNA assay) sensitive to the PIK3CA inhibitor alpelisib.
• Prior immunotherapy is permitted and does not count as chemotherapy.
• The use denosumab or zoledronic is permitted.
• History of previously treated brain metastases with = 4 weeks after definitive surgery and gamma knife/whole brain radiation and not taking steroids.
• = 4 weeks from last oral or IV chemotherapy, small molecule inhibitor, a biologic agent, surgery or radiation.
• Performance status 0-2.
• Adequate organ and marrow function as defined below:
• leukocytes = 3,000/mcL
• Absolute neutrophil count = 1,000/mcL
• platelets = 100,000/mcl
• total bilirubin within institutional upper limit of normal. (= ULN)
• AST (SGOT)/ALT (SPGT) = 3 x ULN (3xULN if liver mets)
• Creatinine = ULN
• A negative serum or urine pregnancy test within 3 days of receiving Day 1 Cycle 1 of leflunomide.
• Women of child-bearing potential and men must agree to use adequate contraception before study entry, for the duration of study participation and for 90 days following completion of therapy. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.
• Recommended methods of birth control are: The consistent use of an approved hormonal contraception such as an intrauterine device (IUD), Double barrier methods (Diaphragm with spermicidal gel or condoms with contraceptive foam), Sexual abstinence (no sexual intercourse) or Sterilization. The use of hormonal forms of birth control is controversial in TNBC and as such women enrolled in the trial are permitted to use birth control pills or depot Provera, only after a documented discussion by the treating physician as too the uncertain risks of hormonal birth control methods in the TNBC population. A female of child-bearing potential is any woman (regardless of sexual orientation, having undergone a tubal ligation, or remaining celibate by choice) who meets the following criteria: Has not undergone a hysterectomy or bilateral oophorectomy; or Has not been naturally postmenopausal for at least 12 consecutive months (i.e., has had menses at any time in the preceding 12 months).
• Ability to understand and the willingness to sign a written informed consent.

Exclusion Criteria:

• Patients who have had chemotherapy or radiotherapy within = 2 weeks before entering the study or those who have not recovered from adverse events due to agents administered more than = 4 weeks earlier.
• Patients may not be receiving any other investigational agents.
• The known history human immunodeficiency virus, acute and chronic Hepatitis B or C, or acute or previously treated tuberculosis.
• Patients with untreated brain metastases should be excluded from this clinical trial because of their poor prognosis and because they often develop progressive neurologic dysfunction that would confound the evaluation of neurologic and other adverse events.
• History of allergic reactions attributed to compounds of similar chemical or biologic composition to leflunomide or teriflunomide.
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
• Patients must not be pregnant or nursing due to the potential for congenital abnormalities and the potential of this regimen to harm nursing infants.

Related Conditions & MeSH terms

• Breast Diseases
• Breast Neoplasms
• Metastatic Triple Negative Breast Cancer
• Triple Negative Breast Neoplasms

Intervention

Drug:
• Leflunomide
Single agent leflunomide

Locations

Country	Name	City	State
United States	Icahn School of Medicine at Mount Sinai	New York	New York
United States	Mt Sinai Chelesa	New York	New York
United States	Mt Sinai West	New York	New York

Sponsors (1)

Lead Sponsor	Collaborator
Joseph Sparano

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum Tolerated Dose (MTD)	3+3 escalation schema. Patients will be enrolled in escalating cohorts of 3 patients per dose level until Dose-limiting Toxicity (DLT) (defined as any grade 3 or higher toxicity seen during the first 3-week cycle of leflunomide). If 0 of 3 patients are observed to have a DLT, the next 3 patients will be enrolled in the next higher dose level cohort. If 2/3 patients experience a DLT, escalation will stop and the previous dose will be defined as the MTD. If 1/3 experiences a DLT, three additional patients will be enrolled at the same dose level. If = 2/6 patients experience a DLT, the next cohort of three patients will be treated at the next dose level. If = 3/6 experience a DLT, the next lower dose level will define the MTD. If at the 50 mg dose/day if 0/3 or = 2/6 patients experience a DLT, then that dose will define the MTD	3 months
Primary	Clinical Benefit Rate (CBR)	Response and progression to be evaluated using the Response Evaluation Criteria in Solid Tumors (RECIST). CBR = Complete Response (CR) + Partial Response (PR) + Stable Disease (SD) for at least 6 months duration	6 months
Secondary	Number of side effects	Number of side effects associated with oral leflunomide using NCI CTCAE v.4.03	6 years
Secondary	Objective Response Rate	Objective Response Rate (proportion of patients with the best overall response of CR or PR) in those who have measurable disease by RECIST	6 years
Secondary	Progression-free survival (PFS)	PFS of women with phosphatase and tensin homolog (PTEN) wild-type and PTEN null expression breast cancers. PFS is defined as the duration of time from the start of treatment to the first occurrence of disease progression or death from any cause, whichever occurs first.	6 years