Cancer Treatment Effects for Breast Cancer and Lymphoma
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to understand how cancer treatments affect sexual and reproductive health in women with breast cancer and lymphoma. Participants will answer surveys about their sexual health and may choose to have blood draws and transvaginal ultrasounds to assess fertility. Women recently diagnosed with breast cancer or lymphoma, who are starting treatment soon, and who have either had a period or been pregnant in the last year, might be suitable candidates. This study is open to both premenopausal and postmenopausal women. As an unphased trial, it offers participants the opportunity to contribute to important research that could improve future care for women facing similar health challenges.
Do I have to stop taking my current medications for this trial?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
Why are researchers excited about this trial?
Researchers are excited about this trial because it aims to shed light on the sexual and reproductive health of women with breast cancer and lymphoma, areas that are often overlooked in standard care. Unlike typical treatments that focus primarily on cancer eradication, this observational study dives into understanding sexual dysfunction and distress, which are significant quality of life issues for many women. By using detailed surveys and medical assessments like blood draws and transvaginal ultrasounds, the trial seeks to identify the prevalence, severity, and predictors of these issues, potentially guiding future interventions to improve overall patient well-being.
Who Is on the Research Team?
Shari Goldfarb, MD
Principal Investigator
Memorial Sloan Kettering Cancer Center
Are You a Good Fit for This Trial?
Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Observational Study
Participants complete comprehensive questionnaires related to sexual and reproductive function
Follow-up
Participants are monitored for changes in sexual and reproductive health, with follow-up questionnaires administered
What Are the Treatments Tested in This Trial?
Interventions
- Blood draw
- Surveys
- Transvaginal ultrasounds
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
This study is a prospective, observational, longitudinal study assessing the prevalence of sexual dysfunction and distress in premenopausal and postmenopausal women with Diffuse Large B-cell Lymphoma or Hodgkin's Lymphoma. This study will also evaluate the severity, time course, and predictors of sexual dysfunction. Lymphoma patients and survivors will be administered surveys of comprehensive questionnaires related to sexual function. In the case that participants miss the follow up questionnaires, study staff may contact the patient by phone to request and record the patients" responses. The study staff may also mail the missed questionnaires to each patient.
This study is a prospective, observational, longitudinal study assessing the prevalence of sexual dysfunction and distress in premenopausal and postmenopausal women with breast cancer. This study will also evaluate the severity, time course, and predictors of sexual dysfunction. Breast cancer patients and survivors will be administered surveys of comprehensive questionnaires related to sexual function. In the case that participants miss the follow up questionnaires, study staff may contact the patient by phone to request and record the patients" responses. The study staff may also mail the missed questionnaires to each patient.
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Who Is Running the Clinical Trial?
Memorial Sloan Kettering Cancer Center
Lead Sponsor
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