Evaluation of efficacy and optimal therapeutic parameters of ALA-PDT in the management of HPV-associated cervical intraepithelial neoplasia grade I - Summary - MDSpire

Evaluation of efficacy and optimal therapeutic parameters of ALA-PDT in the management of HPV-associated cervical intraepithelial neoplasia grade I

  • By

  • Qian Yu

  • Ling Wei

  • Lirui Wu

  • Suning Chen

  • Bo Liu

  • Lianlian Gao

  • July 10, 2026

  • 0 min

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Objective:

To evaluate the effectiveness and safety of aminolevulinic acid photodynamic therapy (ALA-PDT) for HPV-associated cervical intraepithelial neoplasia grade I (CIN I) and to determine optimal treatment parameters.

Approach:
  • Study Design: 240 patients diagnosed with CIN I were divided into four groups based on ALA application time and light exposure duration, receiving treatment every 2 weeks for four sessions.
  • Treatment Groups: Group A1: 3-hour application, 30-minute light exposure; Group A2: 3-hour application, 40-minute light exposure; Group B1: 5-hour application, 30-minute light exposure; Group B2: 5-hour application, 40-minute light exposure.
  • Follow-Up: Patients were followed for 12 months post-treatment, with assessments at 3 and 6 months for HPV testing, TCT, and colposcopy.
Key Findings:
  • Significant decrease in HPV positivity rates and increase in negative conversion rates at 3 and 6 months across all groups.
  • Group B2 showed the greatest improvements in treatment outcomes.
  • Group B2 had the highest cure rate and lowest recurrence rate.
  • HPV16 and HPV18 were positively correlated with the cure rate.
Interpretation:

ALA-PDT is reported to be effective for treating HPV-associated CIN I, with identified treatment parameters of a 5-hour ALA application and 40-minute light exposure.

Limitations:
  • The study did not assess long-term outcomes beyond 12 months.
  • The sample size for each group may limit the generalizability of the findings.
Conclusion:

ALA-PDT demonstrates efficacy in treating HPV-related CIN I.

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