Fertility Preservation Using Tamoxifen and Letrozole in Estrogen Sensitive Tumors Trial (TALES)
Primary Purpose
Infertility
Status
Recruiting
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Tamoxifen
Letrozole
Sponsored by
About this trial
This is an interventional treatment trial for Infertility focused on measuring Fertility Preservation, Breast Cancer
Eligibility Criteria
Inclusion Criteria:
- New breast cancer diagnosis
- Has not yet begun chemotherapy
- Desires to undergo ovarian stimulation and oocyte retrieval prior to cancer treatment
- Age 18 years old or greater
Exclusion Criteria:
- Chemotherapy has already commenced or been completed
- History of recurrent breast cancer (with a prior history of chemotherapy)
- Stage IV breast cancer diagnosis (metastases remote from the breast)
- Patient's oncologist advises against the trial - in which case they can choose to receive stimulation with letrozole+gonadotropin
- Does not plan to undergo ovarian stimulation and oocyte retrieval prior to diagnosis
- Any significant concurrent disease, illness, or psychiatric disorder that would compromise patient safety or compliance, interfere with consent, study participation, follow-up, or interpretation of study results
- Age less than 18 years old
Sites / Locations
- University of California at San FranciscoRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
No Intervention
Arm Label
ER Positive - Letrozole
ER Positive - Tamoxifen
ER Negative
Arm Description
Outcomes
Primary Outcome Measures
Mature Oocyte Yield
To determine if the assigned stimulation regimen will result in a difference in mature (meiosis II) oocyte yield in patients with breast cancer who undergo ovarian stimulation for fertility preservation. An Effect Size of 3 mature oocytes, based on clinically significant difference of 2 embryos to transfer. An average of 2 embryos are transferred per freeze-thaw cycle. If ~75% of mature oocytes will become embryos that can be frozen, then 3 mature oocytes should yield ~2 embryos for transfer. This effect size would effectively mean an additional event of embryos transferred.
Secondary Outcome Measures
Compare change in estrogen levels during the ovarian stimulation cycle
Estrogen level data will be collected at baseline and after completion of the stimulation cycle
Compare change in progesterone levels during the ovarian stimulation cycle
Progesterone level data will be collected at baseline and after completion of the stimulation cycle
Compare change in androgen levels during the ovarian stimulation cycle
Androgen level data will be collected at baseline and after completion of the stimulation cycle
Compare change in estrogen in follicular fluid
Estrogen levels in follicular fluid will be collected at baseline and after completion of the stimulation cycle
Compare change in letrozole in follicular fluid
Letrozole levels in follicular fluid will be collected at baseline and after completion of the stimulation cycle
Compare change in tamoxifen in follicular fluid
Tamoxifen levels in follicular fluid will be collected at baseline and after completion of the stimulation cycle
Compare duration of stimulation (days) and total gonadotropin dose
Number if competent oocytes on day 3 of embryo culture
To assess embryo quality, if applicable, on day 3 of embryo culture, a measure of the developmental competence of the oocytes.
Number if competent oocytes on day 5 of embryo culture
To assess embryo quality, if applicable, on day 5 of embryo culture, a measure of the developmental competence of the oocytes.
Full Information
NCT ID
NCT03011684
First Posted
January 4, 2017
Last Updated
May 1, 2023
Sponsor
University of California, San Francisco
1. Study Identification
Unique Protocol Identification Number
NCT03011684
Brief Title
Fertility Preservation Using Tamoxifen and Letrozole in Estrogen Sensitive Tumors Trial
Acronym
TALES
Official Title
Fertility Preservation Using Tamoxifen and Letrozole in Estrogen Sensitive Tumors Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 21, 2016 (Actual)
Primary Completion Date
January 31, 2024 (Anticipated)
Study Completion Date
January 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Latrogenic infertility as a result of cancer treatment has a profound effect on long-term quality of life in survivors of reproductive-age cancers. Oocyte cryopreservation prior to cancer treatment has been associated with improved quality of life, with a potential ability to reduce long-term decision-related regret in cancer survivors. Though letrozole plus gonadotropin and and tamoxifen plus gonadotropin are currently routinely used worldwide in ovarian stimulation cycles for fertility preservation in patients with estrogen-receptor-positive breast cancer, it is not clear which of the two might lead to improved oocyte yield. Improved knowledge about the efficacy of these medications, with regard to oocyte yield, has the potential to significantly improve quality of life in reproductive-age breast cancer survivors.
Detailed Description
Purpose:
Our primary objective is to determine whether concomitant administration of tamoxifen 20 mg oral with gonadotropins (tamoxifen-gonadotropin) versus a starting dose of letrozole 5 mg oral with gonadotropins (letrozole-gonadotropin) will result in a difference in mature oocyte yield during our routine ovarian stimulation protocol for fertility preservation for Estrogen-Receptor-Positive (ER+) breast cancer.
Specific Aims: Each of the following aims will include a primary comparison and secondary comparisons.
Primary aim: The primary aim will be to compare patients with ER+ breast cancer who are treated with letrozole-gonadotropin versus patients with ER+ breast cancer who are treated tamoxifen-gonadotropin with regard to ovarian stimulation outcomes.
Primary comparison:
1) To determine if the assigned stimulation regimen will result in a difference in mature (meiosis II) oocyte yield in patients with breast cancer who undergo ovarian stimulation for fertility preservation.
Secondary comparison:
To compare estrogen, progesterone, and androgen levels during the ovarian stimulation cycle.
To compare estrogen, letrozole, and tamoxifen levels in follicular fluid.
To compare duration of stimulation (days) and total gonadotropin dose (international units of FSH).
To assess embryo quality, if applicable, on day 3 and day 5 of embryo culture, a measure of the developmental competence of the oocytes.
Experimental comparison:
To compare clinical pregnancy rates when cryopreserved tissue is eventually utilized among patients from the assigned stimulation regimens. This comparison is labeled experimental because of the remoteness of such an outcome from our present study.
Secondary Aim: We will repeat the above comparisons among patients with ER+ breast cancer who are treated with tamoxifen-gonadotropin versus a prospectively-obtained reference group of patients with Estrogen-Receptor-Negative (ER-) breast cancer who are treated gonadotropin alone. We will then again repeat the above comparisons among patients with ER+ breast cancer who are treated letrozole-gonadotropin versus patients with ER- breast cancer who are treated gonadotropin alone.
Experimental Design and Methods:
Study population:
The target population is reproductive-age women who have been recently diagnosed with ER+ breast cancer and choose to undergo oocyte or embryo cryopreservation prior to chemotherapy treatment. All eligible women will be asked to join the study at their initial University of California, San Francisco (UCSF) fertility preservation consult. Study participants will be recruited from the Reproductive Endocrinology Clinic at University of California, San Francisco Center for Reproductive Health. A consecutive sample with ER- disease will also be recruited at the same type of visit. They will be asked to take part in the gonadotropin only stimulation group, which will be used for a secondary aim.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility
Keywords
Fertility Preservation, Breast Cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
144 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
ER Positive - Letrozole
Arm Type
Experimental
Arm Title
ER Positive - Tamoxifen
Arm Type
Experimental
Arm Title
ER Negative
Arm Type
No Intervention
Intervention Type
Drug
Intervention Name(s)
Tamoxifen
Intervention Description
For ER Positive Randomization
Intervention Type
Drug
Intervention Name(s)
Letrozole
Intervention Description
For ER Positive Randomization
Primary Outcome Measure Information:
Title
Mature Oocyte Yield
Description
To determine if the assigned stimulation regimen will result in a difference in mature (meiosis II) oocyte yield in patients with breast cancer who undergo ovarian stimulation for fertility preservation. An Effect Size of 3 mature oocytes, based on clinically significant difference of 2 embryos to transfer. An average of 2 embryos are transferred per freeze-thaw cycle. If ~75% of mature oocytes will become embryos that can be frozen, then 3 mature oocytes should yield ~2 embryos for transfer. This effect size would effectively mean an additional event of embryos transferred.
Time Frame
Up to 2 weeks
Secondary Outcome Measure Information:
Title
Compare change in estrogen levels during the ovarian stimulation cycle
Description
Estrogen level data will be collected at baseline and after completion of the stimulation cycle
Time Frame
Up to 2 weeks
Title
Compare change in progesterone levels during the ovarian stimulation cycle
Description
Progesterone level data will be collected at baseline and after completion of the stimulation cycle
Time Frame
Up to 2 weeks
Title
Compare change in androgen levels during the ovarian stimulation cycle
Description
Androgen level data will be collected at baseline and after completion of the stimulation cycle
Time Frame
Up to 2 weeks
Title
Compare change in estrogen in follicular fluid
Description
Estrogen levels in follicular fluid will be collected at baseline and after completion of the stimulation cycle
Time Frame
Up to 2 weeks
Title
Compare change in letrozole in follicular fluid
Description
Letrozole levels in follicular fluid will be collected at baseline and after completion of the stimulation cycle
Time Frame
Up to 2 weeks
Title
Compare change in tamoxifen in follicular fluid
Description
Tamoxifen levels in follicular fluid will be collected at baseline and after completion of the stimulation cycle
Time Frame
Up to 2 weeks
Title
Compare duration of stimulation (days) and total gonadotropin dose
Time Frame
Up to 2 weeks
Title
Number if competent oocytes on day 3 of embryo culture
Description
To assess embryo quality, if applicable, on day 3 of embryo culture, a measure of the developmental competence of the oocytes.
Time Frame
Up to 2 weeks
Title
Number if competent oocytes on day 5 of embryo culture
Description
To assess embryo quality, if applicable, on day 5 of embryo culture, a measure of the developmental competence of the oocytes.
Time Frame
Up to 2 weeks
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
New breast cancer diagnosis
Has not yet begun chemotherapy
Desires to undergo ovarian stimulation and oocyte retrieval prior to cancer treatment
Age 18 years old or greater
Exclusion Criteria:
Chemotherapy has already commenced or been completed
History of recurrent breast cancer (with a prior history of chemotherapy)
Stage IV breast cancer diagnosis (metastases remote from the breast)
Patient's oncologist advises against the trial - in which case they can choose to receive stimulation with letrozole+gonadotropin
Does not plan to undergo ovarian stimulation and oocyte retrieval prior to diagnosis
Any significant concurrent disease, illness, or psychiatric disorder that would compromise patient safety or compliance, interfere with consent, study participation, follow-up, or interpretation of study results
Age less than 18 years old
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ange Wang, MD
Phone
415-353-7475
Email
Ange.Wang@ucsf.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mitchell Rosen, MD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California at San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ange Wang, M.D.
Phone
415-353-7475
Email
Ange.Wang@ucsf.edu
First Name & Middle Initial & Last Name & Degree
Mitchell Rosen, M.D.
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34312774
Citation
Letourneau J, Juarez-Hernandez F, Wald K, Ribeiro S, Wang A, McCulloch CE, Mok-Lin E, Dolezal M, Chien AJ, Cedars MI, Rosen M. Concomitant tamoxifen or letrozole for optimal oocyte yield during fertility preservation for breast cancer: the TAmoxifen or Letrozole in Estrogen Sensitive tumors (TALES) randomized clinical trial. J Assist Reprod Genet. 2021 Sep;38(9):2455-2463. doi: 10.1007/s10815-021-02273-3. Epub 2021 Jul 26.
Results Reference
derived
Learn more about this trial
Fertility Preservation Using Tamoxifen and Letrozole in Estrogen Sensitive Tumors Trial
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