# Novel Functional Anatomic and Biomarker Indices of Radiation-Induced Female Sexual Toxicities in a Multi-Center Cohort

> **NIH NIH DP5** · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · 2022 · $413,946

## Abstract

Project Summary Abstract
In 2020, about 1 million female patients in the US will be living with pelvic cancers, and roughly half of them will
have received radiation during their course of treatment. The importance of optimizing cancer-directed and
supportive therapies to minimize the adverse effects of radiation and improve quality of life is increasingly
recognized. Among the many aspects of quality of life adversely impacted by cancer treatment is the ability to
continue engaging in pleasurable sexual behaviors, an essential human function throughout the lifespan, and a
clinical problem long overlooked in female cancer survivors. Current classifications of toxicity and normal tissues
in radiation oncology account only poorly for the anatomy and critical function of female erectile tissues (arousal
and orgasm) with respect to such patients' capacities to engage in pleasurable sexual behaviors. In addition, it
has yet to be tested whether observed alterations of vaginal and stool microbiome ecology after radiotherapy
contribute to increased susceptibility to radiation-induced vaginal toxicity and sexual dysfunction, as has been
explored recently in the context of radiation-induced gastrointestinal toxicity. Because roughly 70% of women
with pelvic malignancies now survive at least 5 years, it is imperative to identify predictors and mechanisms of
long-term female sexual dysfunction to improve quality of life given the significant role of sexual activity in overall
well-being. To accelerate advances in mitigating or preventing pelvic radiotherapy-associated female sexual
dysfunction, my proposed research aims to 1) establish a functional anatomic-domain (dermatologic, vaginal,
erectile) classification of long-term radiation-related sexual dysfunction in a multi-center, longitudinal cohort of
female patients undergoing pelvic radiotherapy; 2) define and/or validate novel dosimetric predictors of sexual
dysfunction in each anatomic domain; and, 3) identify quantitative imaging and microbiome biomarker indices of
radiation damage to specific sexual organs. My proposed study will be the first to analyze the effects of
radiotherapy on the erectile anatomic organs in females, and will thereby both elucidate the anatomic bases of
adverse sexual function outcomes, especially those related to arousal and orgasm, and advance overall
understanding of radiation effects for all female sexual anatomic domains. These advances will enable redesign
of radiotherapy protocols to improve such outcomes and identification of imaging biomarkers to assess dose-
volume response and the effectiveness of such interventions. In addition, we will be the first to test the
hypothesis that observed alterations of vaginal and stool microbiome ecology contribute to increased
susceptibility to radiation-induced vaginal toxicity and sexual dysfunction. I aim to pioneer key discoveries in
these underrepresented scientific areas to provide an innovative, tailored approaches to preven...

## Key facts

- **NIH application ID:** 10488662
- **Project number:** 5DP5OD031876-02
- **Recipient organization:** ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
- **Principal Investigator:** Deborah Catherine Marshall
- **Activity code:** DP5 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2022
- **Award amount:** $413,946
- **Award type:** 5
- **Project period:** 2021-09-14 → 2026-08-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10488662

## Citation

> US National Institutes of Health, RePORTER application 10488662, Novel Functional Anatomic and Biomarker Indices of Radiation-Induced Female Sexual Toxicities in a Multi-Center Cohort (5DP5OD031876-02). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10488662. Licensed CC0.

---

*[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*
