Breast Cancer Clinical Trial

Longitudinal Sexual and Reproductive Health Study of Women With Breast Cancer and Lymphoma

Summary

The purpose of this study is to see how cancer treatment affects sexual and reproductive function. The patient will also be asked to participate in blood draws to see if and how cancer treatment affects the ovaries and the ability to have children (fertility). These blood draws are optional and the patient can still participate in the questionnaire portion of the study even if they choose not to have their blood drawn.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Subject Inclusion Criteria for Cohort of Premenopausal Women with Early Stage Breast Cancer and Lymphoma

Women, 18 years of age and older

Premenopausal women at time of diagnosis who have either been pregnant or had at least one menstrual period in the last 12 months

Note: premenopausal women at time of diagnosis who have not been pregnant or have not had at least one menstrual period in the last 12 months are able to participate only if they have had an intrauterine device (IUD) in place within the last 12 months.
Women with newly diagnosed breast cancer (stage 0-III) who are within 1 month of starting systemic treatment or women with any aggressive lymphoma being treated with first line therapy with curative intent.
Breast cancer patients with any receptor type
English speaking
Able to participate in the informed consent process

Subject Inclusion Criteria for Tamoxifen Only Subset of Cohort of Premenopausal Women with Early Stage Breast Cancer and Lymphoma

Women, 18 years of age and older.

Premenopausal women at time of diagnosis who have either been pregnant or had at least one menstrual period in the last 12 months

Note: premenopausal women at time of diagnosis who have not been pregnant or have not had at least one menstrual period in the last 12 months are able to participate only if they have had an intrauterine device (IUD) in place within the last 12 months.
Women with newly diagnosed breast cancer (stage 0-III) who have not yet started treatment and are planning to start Tamoxifen as their only form of systemic treatment within one month
Breast cancer patients with any receptor type
English speaking
Able to participate in the informed consent process

Subject Inclusion Criteria for Cohort of Postmenopausal Women with Early Stage Breast Cancer and Lymphoma

Women, 18 years of age and older.
Postmenopausal women at time of diagnosis who have been without period for ≥ 2 years.
Women with newly diagnosed breast cancer (stage 0-III) who are within 1 month of starting systemic treatment or women with any aggressive lymphoma being treated with first line therapy with curative intent.
Breast cancer patients with any receptor type
English speaking
Able to participate in the informed consent process

Exclusion Criteria:

Subject Exclusion Criteria for both Pre and Postmenopausal Women with Early Stage Breast Cancer and Lymphoma

Active secondary cancer requiring cytotoxic chemotherapy
Prior systemic treatment for a malignancy

Study is for people with:

Breast Cancer

Estimated Enrollment:

400

Study ID:

NCT01788839

Recruitment Status:

Recruiting

Sponsor:

Memorial Sloan Kettering Cancer Center

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There are 7 Locations for this study

See Locations Near You

Memorial Sloan Kettering Basking Ridge
Basking Ridge New Jersey, 07920, United States More Info
Shari Goldfarb, MD
Contact
646-888-5080
Memorial Sloan Kettering Monmouth
Middletown New Jersey, 07748, United States More Info
Shari Goldfarb, MD
Contact
646-888-5080
Memorial Sloan Kettering Bergen
Montvale New Jersey, 07645, United States More Info
Shari Goldfarb, MD
Contact
646-888-5080
Memorial Sloan Kettering Commack
Commack New York, 11725, United States More Info
Shari Goldfarb, MD
Contact
646-888-5080
Memorial Sloan Kettering Westchester
Harrison New York, 10604, United States More Info
Shari Goldfarb, MD
Contact
646-888-5080
Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States More Info
Shari Goldfarb, MD
Contact
646-888-5080
Jeanne Carter, MD
Contact
646-888-5076
Memorial Sloan Kettering Nassau
Uniondale New York, 11553, United States More Info
Shari Goldfarb, MD
Contact
646-888-5080

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

400

Study ID:

NCT01788839

Recruitment Status:

Recruiting

Sponsor:


Memorial Sloan Kettering Cancer Center

How clear is this clinincal trial information?

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