Letrozole in Women With Advanced Estrogen/Progesterone Receptor Positive Uterine Leiomyosarcoma

Dana-Farber Cancer Institute

Status and phase

Completed

Phase 2

Conditions

Leiomyosarcoma

Treatments

Drug: letrozole

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00856050

08-341

Details and patient eligibility

About

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).

Full 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

Enrollment

27 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

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