Screening for gonadal malignancy in androgen insensitivity syndrome: A systematic review

Najva Mazhari1, Andrew Freedman1, Caroline Marshall2

  • 1Departments of Urology and Pediatrics, Cedars Sinai Medical Center, Los Angeles, CA, USA.

PubMed
Abstract

Insights

Standardized screening for malignancy in Androgen Insensitivity Syndrome (AIS) is lacking. Current methods, often expert-based, show limitations in detecting early-stage tumors, necessitating informed patient consent regarding gonadal retention risks.

Area of Science:

  • Endocrinology
  • Oncology
  • Genetics

Background:

  • Gonadectomy was historically standard for Androgen Insensitivity Syndrome (AIS) due to malignancy concerns.
  • This practice is debated due to the benefits of endogenous hormone production and low prepubertal tumor risk.
  • Uncertainty remains regarding long-term malignancy risks in AIS patients.

Purpose of the Study:

  • To review existing screening protocols for gonadal malignancy in AIS.
  • To evaluate the evidence supporting the effectiveness of current screening strategies.
  • To identify ideal screening methods for early detection of premalignant/malignant changes.

Main Methods:

  • Systematic review following PRISMA-P guidelines.
  • Searched multiple databases (PubMed, Scopus, etc.) for studies on AIS, gonadal tumors, and screening.
  • Analyzed data on screening modalities, frequencies, sensitivity, specificity, and protocol effectiveness.

Main Results:

  • 28 studies met inclusion criteria; most recommendations were expert opinion-based.
  • Frequently cited modalities included biopsy and ultrasound, but protocols varied significantly.
  • Limited evidence exists for screening effectiveness; imaging showed limitations in detecting pre-malignant lesions.

Conclusions:

  • A standardized screening strategy for AIS-associated malignancy is absent.
  • Current screening methods lack robust clinical evidence and are largely based on expert consensus.
  • Patients retaining gonads require counseling on risks due to insufficient evidence supporting current screening protocols.

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