Stereotactic Body Radiation Therapy for Early Stage Prostate Cancer: Outcomes from a Single Institution Study Stereotactic Body Radiation Therapy for Early Stage Prostate Cancer: Outcomes from a Single Institution Study Debra Freeman, MD Jay Friedland, MD Naples Radiation Oncology, PA
The Balancing Act ConvenienceInvasiveToxicityEfficacy IMRTLowNoLowHigh LDRBrachyTxHigh Yes X 1 ModHigh HDRBrachyTxModerate Yes X 2 Low/Mod Very High SBRTHighNo Very Low TBD
Experience to Date Experience to Date First patient treated in Jan First patient treated in Jan Initiated Monotherapy protocol in Feb Initiated Monotherapy protocol in Feb Total patients treated: 334 Monotherapy: 276 Boost: 58 (Jan Apr. 2008) (Jan Apr. 2008)
(n=201) Monotherapy Group (n=201) At least 6 months follow-up At least 6 months follow-up Stage T1cN0M0 to T2cN0M0 Stage T1cN0M0 to T2cN0M0 Mean age = 69.3 (49-87) Mean age = 69.3 (49-87) Mean prostate volume = 46.3cc Mean prostate volume = 46.3cc Mean initial PSA = 6.0 ng/ml Mean initial PSA = 6.0 ng/ml Gleason score (3+3) = 150 pts Gleason score (3+3) = 150 pts (3+4) = 39 pts (3+4) = 39 pts (4+3) = 8 pts (4+3) = 8 pts
Hormonal Therapy 174 Patients treated without hormonal therapy: 22% with Gleason score >7 mean prostate volume = 45cc 27 Patients treated with neoadjuvant hormonal therapy: 42% with Gleason score >7 mean prostate volume = 57cc
CyberKnife MonoTx Dose Feb 2005-Dec 2006: 7.0Gy X 5 fractions (35Gy) Feb 2005-Dec 2006: 7.0Gy X 5 fractions (35Gy) Jan 2007-present: 7.25Gy X 5 fractions (36.25Gy) Jan 2007-present: 7.25Gy X 5 fractions (36.25Gy)
BED for Prostate Monotherapy Treatment Regimens 81Gy IMRT/ 45fx / 9 weeks BED 1.5 = 178 BED 3 = 130 HDR 9.5Gy X 4fx BED 1.5 = 279 BED 3 = 158 HDR 8.55Gy X 4fx BED 1.5 = 229 BED 3 = 132 CK 7Gy X 5fx BED 1.5 = 198 BED 3 = 117 CK 7.25Gy X 5fx BED 1.5 = 212 BED 3 = 124 CK 9.5Gy X 4fx BED 1.5 = 279 BED 3 = 158
Patient Prep
Fiducial Placement CyberKnife fiducials CyberKnife fiducials Stainless steel screws Stainless steel screws Gold seeds Gold seeds Our Prostate Fiducial Placement Our Prostate Fiducial Placement Use stranded gold seeds (2 seeds per needle, 2 cm spacing) Use stranded gold seeds (2 seeds per needle, 2 cm spacing) Patient in dorsal lithotomy position Patient in dorsal lithotomy position Place fiducials transperineally using TRUS and standard implant template Place fiducials transperineally using TRUS and standard implant template 2 needle sticks, drop off 4 seeds 2 needle sticks, drop off 4 seeds
Patient Prep Low residue diet before imaging and during treatment week (bowel gas) Low residue diet before imaging and during treatment week (bowel gas) Fleet enema 1 to 2 hours before imaging and treatment Fleet enema 1 to 2 hours before imaging and treatment Empty bladder 1 to 2 hours before treatment, then drink specified volume of water Empty bladder 1 to 2 hours before treatment, then drink specified volume of water
Clinical Example Treatment Planning CT CT at Time of Treatment
Contouring
PTV: gland expanded 5 mm in each direction except posteriorly where it is expanded 3 mm
Collimator Selection 12 collimators 12 collimators May use one or more collimators during a treatment session May use one or more collimators during a treatment session This study used 2 collimators for all prostate treatments This study used 2 collimators for all prostate treatments Large collimator to minimize tmt time Large collimator to minimize tmt time Small collimator to paint dose conformally at interfaces Small collimator to paint dose conformally at interfaces Dia. (mm) The IRIS is here! Can change collimator size for every beam
130 – 160 beams 35,000 – 45,000 mu’s prescribe to 85% isodose Max / Min dose = 1.20 (mean) PTV coverage > 95% CI = Treatment time: minutes Typical Prostate Plan: This Study
Criteria of Acceptability: Rectum % RectumSuggested Dose Limit (Gy) (2 Gy/fx) Calculated Dose Limit (Gy) (7.25 Gy/fx, 5 fx, King) (50 RTOG) 60 (1) (2) (1) (2) (1) (2) (1) (2) Huang et al., Late Rectal Toxicity: Dose-Volume Effects of Conformal Radiotherapy for Prostate Cancer, IJROBP, Vol. 54, No. 5, , RTOG P-0126
Results
PSA Response to CyberKnife
% achieving given PSA level by duration of follow-up PSA level1 Year (62 pts) 2 Years (54 pts) 3 Years (19 pts) ≤ 1.0 ng/ml56%84%95% ≤ 0.6 ng/ml39%54%68% ≤ 0.4 ng/ml19%43%53% ≤ 0.2 ng/ml6%14%32% PSA Response to CyberKnife
Acute Toxicity Urinary hesitancy, urgency, frequency (Day 3-10) Urinary hesitancy, urgency, frequency (Day 3-10) Tenesmus/ rectal discomfort (Day 5-8) Tenesmus/ rectal discomfort (Day 5-8) Mild diarrhea (Day 5-8) Mild diarrhea (Day 5-8) Rx: Flomax Rx: Flomax Lomotil Lomotil Decadron Decadron Anusol-HC supp. Anusol-HC supp. Activia yogurt Activia yogurt
AUA Scores after CyberKnife SBRT
GI Toxicity RAS scores show pattern similar to AUA (minimal acute change with return to baseline by 4 months) Two pts. with documented radiation proctitis/rectal bleeding Developed <1yr post-tx Both pts. diabetic, on chronic Coumadin Treated with argon laser therapy; bleeding resolved
SHIM Scores After CyberKnife SBRT
E.D.(?) 82% of pts. maintained “erections sufficient for intercourse” at 3 yrs. (based on question #2 of SHIM)
Summary CyberKnife monotherapy appears to produce a reasonable early decline of PSA in low risk patients. CyberKnife monotherapy appears to produce a reasonable early decline of PSA in low risk patients. The acute toxicity of CyberKnife monotherapy is acceptable. Late toxicity is thus far extremely low. The acute toxicity of CyberKnife monotherapy is acceptable. Late toxicity is thus far extremely low. CyberKnife is a noninvasive and convenient treatment option for patients with early stage prostate cancer. CyberKnife is a noninvasive and convenient treatment option for patients with early stage prostate cancer. Prostate cancer patients treated with CyberKnife should optimally be enrolled on clinical research protocols. Funded protocols are currently available. Prostate cancer patients treated with CyberKnife should optimally be enrolled on clinical research protocols. Funded protocols are currently available.