Subgroup analysis of patients with localized prostate cancer treated within the Dutch-randomized dose escalation trial
Purpose: To investigate the effect of dose escalation within prognostic risk groups in prostate cancer. Patients and methods: Between 1997 and 2003, 664 patients with localized prostate cancer were randomly assigned to receive 68- or 78-Gy of radiotherapy. Two prognostic models were examined: a risk group model (low-, intermediate-, and high-risk) and PSA-level groupings. High-risk patients with hormonal therapy (HT) were analyzed separately. Outcome variable was freedom from failure (FFF) (clinical failure or PSA nadir + 2 μg/L). Results: In relation to the advantage of high-dose radiotherapy, intermediate-risk patients benefited most from dose escalation. However no significant heterogeneity could be demonstrated between the risk groups. For two types of PSA-level groupings: PSA < 10 and ≥10 μg/L, and <8, 8-18 and >8 μg/L, the test for heterogeneity was significant (p = 0.03 and 0.05, respectively). Patients with PSA 8-18 μg/L (n = 297, HR = 0.59) derived the greatest benefit from dose escalation. No heterogeneity could be demonstrated for high-risk patients with and without HT. Conclusion: Intermediate-risk group derived the greatest benefit for dose escalation. However, from this trial no indication was found to exclude low-risk or high-risk patients from high-dose radiotherapy. Patients could be selected for high-dose radiotherapy based on PSA-level groupings: for patients with a PSA < 8 μg/L high-dose radiotherapy is probably not indicated, but should be confirmed in other randomized studies.
|Keywords||Dose escalation, Prostate cancer, Radiotherapy, Randomized trial, Subgroup analysis|
|Persistent URL||dx.doi.org/10.1016/j.radonc.2010.02.022, hdl.handle.net/1765/20264|
|Journal||Radiotherapy & Oncology|
Al-Mamgani, A, Heemsbergen, W.D, Levendag, P.C, & Lebesque, J.V. (2010). Subgroup analysis of patients with localized prostate cancer treated within the Dutch-randomized dose escalation trial. Radiotherapy & Oncology, 96(1), 13–18. doi:10.1016/j.radonc.2010.02.022