Journal article
Phase I dose-escalation study of stereotactic body radiation therapy for low- and intermediate-risk prostate cancer
Journal of clinical oncology, Vol.29(15), pp.2020-2026
05/20/2011
DOI: 10.1200/JCO.2010.31.4377
PMCID: PMC3138546
PMID: 21464418
Abstract
To evaluate the tolerability of escalating doses of stereotactic body radiation therapy in the treatment of localized prostate cancer. Eligible patients included those with Gleason score 2 to 6 with prostate-specific antigen (PSA) ≤ 20, Gleason score 7 with PSA ≤ 15, ≤ T2b, prostate size ≤ 60 cm(3), and American Urological Association (AUA) score ≤ 15. Pretreatment preparation required an enema and placement of a rectal balloon. Dose-limiting toxicity (DLT) was defined as grade 3 or worse GI/genitourinary (GU) toxicity by Common Terminology Criteria of Adverse Events (version 3). Patients completed quality-of-life questionnaires at defined intervals. Groups of 15 patients received 45 Gy, 47.5 Gy, and 50 Gy in five fractions (45 total patients). The median follow-up is 30 months (range, 3 to 36 months), 18 months (range, 0 to 30 months), and 12 months (range, 3 to 18 months) for the 45 Gy, 47.5 Gy, and 50 Gy groups, respectively. For all patients, GI grade ≥ 2 and grade ≥ 3 toxicity occurred in 18% and 2%, respectively, and GU grade ≥ 2 and grade ≥ 3 toxicity occurred in 31% and 4%, respectively. Mean AUA scores increased significantly from baseline in the 47.5-Gy dose level (P = .002) as compared with the other dose levels, where mean values returned to baseline. Rectal quality-of-life scores (Expanded Prostate Cancer Index Composite) fell from baseline up to 12 months but trended back at 18 months. In all patients, PSA control is 100% by the nadir + 2 ng/mL failure definition. Dose escalation to 50 Gy has been completed without DLT. A multicenter phase II trial is underway treating patients to 50 Gy in five fractions to further evaluate this experimental therapy.
Details
- Title: Subtitle
- Phase I dose-escalation study of stereotactic body radiation therapy for low- and intermediate-risk prostate cancer
- Creators
- Thomas P Boike - University of Texas Southwestern, Dallas, TX 75390, USAYair LotanL Chinsoo ChoJeffrey BrindlePaul DeRoseXian-Jin XieJingsheng YanRyan FosterDavid PistenmaaAlida PerkinsSusan CooleyRobert Timmerman
- Resource Type
- Journal article
- Publication Details
- Journal of clinical oncology, Vol.29(15), pp.2020-2026
- DOI
- 10.1200/JCO.2010.31.4377
- PMID
- 21464418
- PMCID
- PMC3138546
- NLM abbreviation
- J Clin Oncol
- ISSN
- 0732-183X
- eISSN
- 1527-7755
- Publisher
- United States
- Grant note
- PC061629 / NCI NIH HHS
- Language
- English
- Date published
- 05/20/2011
- Academic Unit
- Preventive and Community Dentistry; Biostatistics; Dental Research
- Record Identifier
- 9983917765902771
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