Leiomyosarcoma
Conditions
Keywords
estrogen receptor positive, progesterone receptor positive, letrozole
Brief summary
The purpose of this research study is to determine if letrozole is effective at controlling the growth or spread of estrogen and/or progesterone receptor positive uterine leiomyosarcoma. This drug has been used in research studies for other cancers and is currently approved by the FDA for use in breast cancer. Because letrozole lowers hormone levels in the body, it may be helpful to control tumors that express hormone receptors ( ER/PR).
Detailed description
* Participants will take letrozole orally once a day. During the research study the following tests and procedures will be performed: * Visit 1 (Day 1): physical examination, vital signs and blood work * Visit 2 (Day 43): physical examination, vital signs, blood work, CT or MRI scan * Visit 3 (Day 85): physical examination, vital signs, blood work, CT or MRI scan * Participants will remain on the study drug as long as they do not have any serious sife effect and their disease does not get worse
Interventions
DRUGletrozole
Taken orally once a day continuously
Sponsors
Brigham and Women's Hospital
Novartis
Dana-Farber Cancer Institute
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Histologically or cytologically confirmed, advanced estrogen (ER)/progesterone receptor (PR) positive leiomyosarcoma of uterine origin, for which standard multi-modality curative therapies do not exist or are no longer effective * Patients must be postmenopausal. Postmenopausal is defined as any of the following: 1)Bilateral oophorectomy 2) 60 years of age or older 3)Younger than 60 AND amenorrheic for 12 months or more AND follicle stimulating hormone (FSH) and estradiol (E2) within postmenopausal range 4)Ovarian ablation radiotherapy confirmed by FSH and estradiol (E2) level in the postmenopausal range * Evidence of ER and/or PR positivity, either in primary or secondary tumor tissue * Measurable disease outside of a prior irradiated area as defined by RECIST guidelines. A lesion in a previously irradiated area is not eligible for measurable diseae unless there is objective evidence of progression of the lesion prior to study enrollment * 18 years of age or older * Life expectancy of 3 months or more * ECOG Performance Status 0, 1, or 2 * No limit to number of prior chemotherapies or biologics * Normal organ function as outlined in the protocol * Resolution of clinically significant toxicities related to prior therapies
Exclusion criteria
* Pre-menopausal women * Participants who have had systemic anti-cancer therapy within 3 weeks of study entry (8 weeks for nitrosoureas or mitomycin C) * Palliative radiotherapy within 2 weeks of study entry * Major surgery within 2 weeks of study entry * Prior hormonal therapy for the treatment of uterine leiomyosarcoma (prior hormone replacement therapy is allowed) * Participants may not be receiving any other concomitant investigational agents * Uncontrolled brain or central nervous system metastases * History of allergic reactions attributed to compounds of similar chemical or biologic composition to letrozole * 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 * Individuals with a history of a different malignancy, other than cervical cancer in situ, basal cell or squamous cell carcinoma of the skin, are ineligible, except if they have been disease-free for at least 5 years, and are deemed by the investigator to be at low risk for recurrence of that malignancy OR other primary malignancy is neither currently clinically significant nor requiring active intervention
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Progression Free Survival Rate at 12 Weeks | 12 weeks | Data below are reported as progression free rate (%). |
Countries
United States
Participant flow
Pre-assignment details
27 patients were enrolled, and 26 patients received at least one dose of study medication and were included in the analysis.
Participants by arm
| Arm | Count |
|---|---|
| Letrozole letrozole 2.5mg by mouth per day | 26 |
| Total | 26 |
Baseline characteristics
| Characteristic | Letrozole |
|---|---|
| Age, Continuous | 56 years |
| Sex: Female, Male Female | 26 Participants |
| Sex: Female, Male Male | 0 Participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | — / — |
| other Total, other adverse events | 20 / 26 |
| serious Total, serious adverse events | 0 / 26 |
Outcome results
Primary
Progression Free Survival Rate at 12 Weeks
Data below are reported as progression free rate (%).
Time frame: 12 weeks
Population: 27 patients were enrolled, and 26 patients received at least one dose of study medication and were included in the analysis.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Letrozole | Progression Free Survival Rate at 12 Weeks | 46 percentage of participants |