International Journal of Radiation Oncology * Biology * Physics
Volume 57, Issue 5 , Pages 1260-1268, 1 December 2003

Hazards of dose escalation in prostate cancer radiotherapy

Presented at the 44th Annual Meeting of the American Society for Therapeutic Radiology and Oncology, New Orleans, LA, October 9, 2002.

  • Deborah Kuban, M.D.

      Affiliations

    • Department of Radiation Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA
    • Corresponding Author InformationReprint requests to: Deborah Kuban, M.D., Department of Radiation Oncology, Box 97, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030, USA. Tel: 713-792-5862; Fax: 713-794-5573;
  • ,
  • Alan Pollack, M.D., Ph.D.

      Affiliations

    • Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA, USA
  • ,
  • Eugene Huang, M.D.

      Affiliations

    • Department of Radiation Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA
  • ,
  • Larry Levy, M.S.

      Affiliations

    • Department of Biomathematics, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA
  • ,
  • Lei Dong, Ph.D.

      Affiliations

    • Department of Radiation Physics, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA
  • ,
  • George Starkschall, Ph.D.

      Affiliations

    • Department of Radiation Physics, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA
  • ,
  • Isaac Rosen, Ph.D.

      Affiliations

    • Department of Radiation Physics, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA

Received 24 February 2003; received in revised form 30 May 2003; accepted 10 June 2003.

Abstract 

Purpose

To assess the benefit of escalating the dose in definitive prostate cancer radiotherapy vs. the associated risk of complications.

Methods and materials

Between 1987 and 1999, 1087 patients with clinical Stage T1b–T3 adenocarcinoma of the prostate were definitively irradiated without hormonal therapy and had a pretreatment serum prostate-specific antigen (PSA) and Gleason score recorded. The median follow-up was 65 months. Doses ranged from 64 to 78 Gy, with the treatment techniques corresponding to the year of therapy and the prescribed dose. A total of 301 patients were treated on a randomized protocol to either 70 or 78 Gy. Also, 163 patients were treated with three-dimensional conformal therapy and had dose–volume histograms available for review.

Results

Tumor stage, grade, pretreatment PSA level, and radiation dose were all independent predictors of PSA disease-free survival (PSA-DFS) in multivariate analysis. The hazard rate for biochemical failure peaked at 1.5–3 years after radiotherapy. Although a statistically significant dose effect on PSA-DFS was found in the pretreatment PSA levels of those with both ≤10 ng/mL and >10 ng/mL, in those with a pretreatment PSA ≤10 ng/mL, the improvement in outcome was only seen going from a dose level of 64–66 Gy to 68–70 Gy with a 5-year PSA-DFS rate of 66% vs. 81% (p <0.0001). This was also confirmed by the data from the randomized patients who showed no difference in outcome whether treated to 70 Gy or 78 Gy. In patients with a pretreatment PSA level >10 ng/mL, a statistically significant improvement was found in disease-free outcome among the 64–66-Gy, 68–70-Gy, and 78-Gy levels. PSA-DFS was approximately 50% better at each higher dose level at 5 and 8 years after treatment. The dose had a statistically significant impact in both intermediate- and high-risk groups. Rectal morbidity was both dose and volume related. Although at 5 years after therapy, the Grade 2-3 rectal complication rate was twice as high for patients treated to 78 Gy than to 70 Gy, 26% vs. 12%, this risk could be markedly diminished by adhering to dose–volume constraints.

Conclusion

In intermediate- and high-risk prostate cancer patients, although it appears that radiation-dose escalation may improve PSA-DF outcome, the price paid in treatment morbidity can be high without adequate attention to dose–volume constraints of normal tissue. Care must be taken to consider not only the hazard of tumor recurrence but also that of complications.

Keywords:  Prostate cancer, Dose escalation, PSA-DFS, Complications

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PII: S0360-3016(03)00772-7

doi:10.1016/S0360-3016(03)00772-7

International Journal of Radiation Oncology * Biology * Physics
Volume 57, Issue 5 , Pages 1260-1268, 1 December 2003