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Daily Vaginal Dilator Use During Radiation for Women With Squamous Cell Carcinoma of the Anus: Vaginal Wall Dosimetry and Patient-Reported Sexual Function.
Arzola, Angelica; Chang, Enoch; Rooney, Michael K; Corrigan, Kelsey; Das, Prajnan; Ludmir, Ethan B; Koay, Eugene J; Minsky, Bruce D; Smith, Grace L; Messick, Craig; Morris, Van K; Nebgen, Denise; Crane, Christopher H; Holliday, Emma B.
Affiliation
  • Arzola A; Departments of Gastrointestinal Radiation Oncology.
  • Chang E; Departments of Gastrointestinal Radiation Oncology.
  • Rooney MK; Departments of Gastrointestinal Radiation Oncology.
  • Corrigan K; Departments of Gastrointestinal Radiation Oncology.
  • Das P; Departments of Gastrointestinal Radiation Oncology.
  • Ludmir EB; Departments of Gastrointestinal Radiation Oncology.
  • Koay EJ; Departments of Gastrointestinal Radiation Oncology.
  • Minsky BD; Departments of Gastrointestinal Radiation Oncology.
  • Smith GL; Departments of Gastrointestinal Radiation Oncology.
  • Messick C; Colorectal Surgery.
  • Morris VK; Gastrointestinal Medical Oncology.
  • Nebgen D; Gynecologic Oncology and Reproductive Medicine, University of Texas MD Anderson Cancer Center, Houston, Texas.
  • Crane CH; Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Holliday EB; Departments of Gastrointestinal Radiation Oncology. Electronic address: emmaholliday@gmail.com.
Pract Radiat Oncol ; 14(2): e105-e116, 2024.
Article in En | MEDLINE | ID: mdl-37898354
ABSTRACT

PURPOSE:

At our institution, we treat patients with a daily vaginal dilator (VD) during chemoradiation (CRT) for squamous cell carcinoma of the anus (SCCA). We evaluated compliance with daily VD use, radiation dose to the vaginal wall (VW), and anterior vaginal wall (AVW), and patient-reported long-term sexual function. METHODS AND MATERIALS We included women with SCCA who received definitive, intensity-modulated radiation therapy-based CRT. Women who were alive without evidence of disease received a patient-reported outcome survey, which included the Female Sexual Function Index (FSFI). We identified factors associated with FSFI, such as radiation dose to the VW and AVW using linear regression models and used Youden index analysis to estimate a dose cutoff to predict sexual dysfunction.

RESULTS:

Three hundred thirty-nine consecutively treated women were included in the analysis; 285 (84.1%) were treated with a daily VD. Of 184 women alive without disease, 90 patients (49%) completed the FSFI, and 51 (56.7%) were sexually active with valid FSFI scores. All received therapy with a daily VD. Forty-one women (80%) had sexual dysfunction. Univariate analysis showed higher dose to 50% (D50%) of the AVW correlated with worse FSFI (ß -.262; P = .043), worse desire FSFI subscore (ß -.056; P = .003), and worse pain FSFI subscore (ß -.084; P = .009). Younger age correlated with worse pain FSFI subscale (ß .067; P = .026). Age (ß .070; P = .013) and AVW D50% (ß -.087; P = .009) were significant on multivariable analysis. AVW D50% >48 Gy predicted increased risk of sexual dysfunction.

CONCLUSIONS:

Daily VD use is safe and well tolerated during CRT for SCCA. Using a VD during treatment to displace the AVW may reduce the risk for sexual dysfunction. Limiting the AVW D50% <48 Gy may further reduce the risk but additional data are needed to validate this constraint.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sexual Dysfunction, Physiological / Carcinoma, Squamous Cell Limits: Female / Humans Language: En Journal: Pract Radiat Oncol Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sexual Dysfunction, Physiological / Carcinoma, Squamous Cell Limits: Female / Humans Language: En Journal: Pract Radiat Oncol Year: 2024 Document type: Article