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



Status:Recruiting
Conditions:Breast Cancer, Cancer, Lymphoma
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:3/28/2019
Start Date:February 2013
End Date:February 2020
Contact:Shari Goldfarb, MD
Phone:646-888-5080

Use our guide to learn which trials are right for you!

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.


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
We found this trial at
7
sites
1275 York Ave
New York, New York 10021
(212) 639-2000
Phone: 646-888-5080
Memorial Sloan Kettering Cancer Center Memorial Sloan Kettering Cancer Center — the world's oldest and...
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Basking Ridge, New Jersey 07920
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Commack, New York 11725
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500 Westchester Avenue
Harrison, New York 10604
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Middletown, New Jersey 07748
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225 Summit Avenue
Montvale, New Jersey 07645
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Rockville Centre, New York 11570
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Rockville Centre, NY
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