Abstract
Objective
The objective of the study is to demonstrate the feasibility of using [11C]-choline positron-emission tomography (PET)/CT to deliver helical tomotherapy (HT) to the prostate with a simultaneous integrated boost to dominant intraprostatic lesions as a biological target volume for dose escalation.
Methods
Eleven patients with intermediate-risk prostate cancer were included in this virtual planning study. Pretreatment baseline [11C]-choline PET/CT scans were acquired with a PET/CT scanner dynamically in 2-min frames from injection to 40 min post injection. PET data was reconstructed using the RAMLA 3D algorithm and analyzed to identify dominant intraprostatic lesion(s). Dominant lesions were defined as biological target volume(s) (BTV) including all voxels with a standardized uptake value of 75 % or above relative to the maximum standard uptake value (SUV) within the prostate gland. Three target volumes for optimization included the following: PTV78 (BTV + 5 mm margin), PTV68 (prostate + 5 mm posteriorly and 10 mm in all other dimensions), and PTV50 (prostate gland and proximal seminal vesicles + 7 mm margin posteriorly and 10 mm in all other dimensions). Dose constraints on organs at risk were implemented based on a published data using hypofractionated IMRT with long-term follow-up. Helical tomotherapy plans were generated to deliver hypofractionated radiation therapy to these volumes using simultaneous integrated boost in 25 fractions.
Results
Eight patients had one identifiable contiguous BTV, and the other three patients had two noncontiguous BTVs. The mean BTV ratio to prostate volume ratio was 6.03 % (minimum 0.80 %, maximum 13.44 %). Target volume and normal tissue constraints were met in seven of the 11 patients enrolled in the study. Targets and structures in the four patients that did not meet constraints were the bladder (3 patients), peritoneal cavity (2 patients), rectum (1 patient), PTV68 (1 patient), and PTV50 (1 patient).
Conclusion
It is feasible in selected patients to use [11C]-choline PET/CT to deliver hypofractionated dose-escalated helical tomotherapy to dominant intraprostatic lesions with simultaneous integrated boost using clinically established normal tissue constraints.
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References
Brenner DJ, Hall EJ (1999) Fractionation and protraction of radiotherapy of prostate carcinoma. Int J Radiat Oncol Biol Phys 43:1095–1101
Kuban DA, Tucker SL, Dong L et al (2008) Long-term results of the M.D. Anderson randomized dose escalation trial for prostate cancer. Int J Radiat Oncol Biol Phys 70(1):67–74
Zietman AL, DeSilvio ML, Slater JD et al (2005) Comparison of conventional-dose vs. high-dose conformal radiation therapy in clinically localized adenocarcinoma of the prostate: a randomized controlled trial. JAMA 294(10):1233–1239
Peeters S, Heemsbergen WD, Koper P et al (2006) Dose-response in radiotherapy for localized prostate cancer: results of the Dutch multicenter randomized phase III trial comparing 68 Gy of radiotherapy with 78 Gy. J Clin Oncol 24(13):1990–1996
Zelefsky MJ, Yamada Y, Fuks Z et al (2008) Long-term results of conformal radiotherapy for prostate cancer: impact of dose escalation on biochemical tumor control and distant metastases-free survival outcomes. Int J Radiat Oncol Biol Phys
Lucignani G, Paganelli G, Bombardieri E (2004) The use of standardized uptake values for assessing FDG uptake with PET in oncology: a clinical perspective. Nucl Med Commun 25:651–656
Effert PJ, Bares R, Handt S, Wolf JM et al (1996) Metabolic imaging of untreated prostate cancer by positron emission tomography with 18fluorine-labeled deoxyglucose. J Urol 155:994–998
Liu IJ, Zafar MB, Lai YH et al (2001) Fluorodeoxyglucose positron emission tomography studies in diagnosis and staging of clinically organ-confined prostate cancer. Urology 57:108–111
Sanz G, Robles JE, Gimenez M et al (1999) Positron emission tomography with 18fluorine-labelled deoxyglucose: utility in localized and advanced prostate cancer. BJU Int 84:1028–1031
Kao PF, Chou YH, Lai CW (2008) Diffuse FDG uptake in acute prostatitis. Clin Nucl Med 33:308–310
Matthies A, Ezziddin S, Ulrich EM et al (2004) Imaging of prostate cancer metastases with 18F-fluoroacetate using PET/CT. Eur J Nucl Med Mol Imaging 31:797
Ponde DE, Dence CS, Oyama N et al (2007) 18F-fluoroacetate: a potential acetate analog for prostate tumor imaging—in vivo evaluation of 18F-fluoroacetate versus 11C-acetate. J Nucl Med 48:420–428
Fricke E, Machtens S, Hofmann M et al (2003) Positron emission tomography with 11C-acetate and 18F-FDG in prostate cancer patients. Eur J Nucl Med Mol Imaging 30:607–611
Oyama N, Miller TR, Dehdashti F et al (2003) 11C-acetate PET imaging of prostate cancer: detection of recurrent disease at PSA relapse. J Nucl Med 44:549–555
Cimitan M, Bortolus R, Morassut S et al (2006) [18F]fluorocholine PET/CT imaging for the detection of recurrent prostate cancer at PSA relapse: experience in 100 consecutive patients. Eur J Nucl Med Mol Imaging 33:1387–1398
Beheshti M, Imamovic L, Broinger G et al (2010) 18 F choline PET/CT in the preoperative staging of prostate cancer in patients with intermediate or high risk of extracapsular disease: a prospective study of 130 patients. Radiology 254:925–933
Hara T, Kosaka N, Kishi H (1998) PET imaging of prostate cancer using carbon-11-choline. J Nucl Med 39:990–995
Kotzerke J, Prang J, Neumaier B et al (2000) Experience with carbon-11 choline positron emission tomography in prostate carcinoma. Eur J Nucl Med 27:1415–1419
Reske SN, Blumstein NM, Neumaier B, Gottfried HW, Finsterbusch F, Kocot D, Möller P, Glatting G, Perner S (2006) Imaging prostate cancer with 11C-choline PET/CT. J Nucl Med 47:1249–1254
Fowler JF, Ritter MA, Chappell RJ, Brenner DJ (2003) What hypofractionated protocols should be tested for prostate cancer? Int J Radiat Oncol Biol Phys 56:1093–1104
Brenner DJ, Martinez AA, Edmundson GK, Mitchell C, Thames HD, Armour EP (2002) Direct evidence that prostate tumors show high sensitivity to fractionation (low alpha/beta ratio), similar to late-responding normal tissue. Int J Radiat Oncol Biol Phys 52:6–13
D'Souza WD, Thames HD (2001) Is the alpha/beta ratio for prostate cancer low? Int J Radiat Oncol Biol Phys 51:1–3
King CR, Fowler JF (2001) A simple analytic derivation suggests that prostate cancer alpha/beta ratio is low. Int J Radiat Oncol Biol Phys 51:213–214
Pervez N, Small C, MacKenzie M et al (2010) Acute toxicity in high-risk prostate cancer patients treated with androgen suppression and hypofractionated intensity-modulated radiotherapy. Int J Radiat Oncol Biol Phys 76(1):57–64
Kupelian PA, Willoughby TR, Reddy CA et al (2007) Hypofractionated intensity-modulated radiotherapy (70 Gy at 2.5 Gy per fraction) for localized prostate cancer: Cleveland Clinic experience. Int J Radiat Oncol Biol Phys 68(5):1424–1430
Ling CC, Humm J, Larson S et al (2000) Towards multidimensional radiotherapy (MD-CRT): biological imaging and biological conformality. Int J Radiat Oncol Biol Phys 47:551–560
Van Lin ENJ, Futterer J, Heijmink SWT et al (2006) IMRT boost planning on dominant intraprostatic lesions: gold marker-based three-dimensional fusion of CT with dynamic contrast-enhanced and 1H-spectroscopic MRI. Int J Radiat Oncol Biol Phys 65:291–303
Wilson AA, Garcia A, Jin L et al (2000) Radiotracer synthesis from [11C]-iodomethane: a remarkable simply captive solvent method. Nucl Med Biol 27:529–532
Acknowledgments
We thank Lai Schrader for her expertise and invaluable assistance in the accrual and data management of this study, Merlita Lamadrid for the data management, and Heidi Borchers for the administrative assistance in preparing this manuscript.
Conflict of interest
The authors John Amanie, M.D.; Jans Hans-Sonke, Ph.D.; Melinda Wuest, PhD; Colin Field; Nadeem Pervez, M.D.; Albert Murtha, M.D.; Nawaid Usmani, M.D.; Don Yee, M.D.; Brita Danielson, M.D.; Samir Patel, M.D.; Rob Macewan, M.D.; Don Robinson, Ph.D.; John Wilson, Ph.D.; Dyann Lewis, R.T.T.; Matthew Parliament, M.D.; and Alexander J.B. McEwan, M.D. do not have a conflict of interest with respect to this article in accordance with the standards set by the International Committee of Medical Journal Editors (ICMJE).
Ethical statement
All persons gave their informed consent prior to their inclusion in the study.
This study was approved by the appropriate ethics committee and has therefore been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments.
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Amanie, J., Hans-Sonke, J., Wuest, M. et al. [11C]-Choline PET/CT-guided simultaneous integrated boost to dominant intraprostatic lesions using intensity-modulated radiation therapy with helical tomotherapy technique for dose escalation. J Radiat Oncol 4, 87–93 (2015). https://doi.org/10.1007/s13566-014-0176-1
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DOI: https://doi.org/10.1007/s13566-014-0176-1