|Year : 2006 | Volume
| Issue : 4 | Page : 239-241
Prostate brachytherapy: HDR or seed implant
Peter MacCallum Cancer Centre, Melbourne 3002, Australia
K R Das
Peter MacCallum Cancer Centre, Melbourne 3002
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Das K R. Prostate brachytherapy: HDR or seed implant. J Med Phys 2006;31:239-41
" I crave the forgiveness of the learned for giving an interpretation different from the orthodox commentarians in regard to these two verses".
Incidence of prostate cancer among men has been on the increase in India and as per many cancer registries it is sixth in incidence rate. This may be due to the increase in longevity among the population, increased awareness and the early detection with PSA testing. A number of treatment options are now available, which include watchful waiting, radical prostatectomy, external beam irradiation and brachytherapy. Of all these modalities, brachytherapy seems to be very promising for localised prostate cancer in terms of local control, patient convenience, morbidity and cost-effectiveness.
Prostate brachytherapy involves the technique of implanting discrete radiation source either permanently or temporarily in the prostate. Both techniques are used either in conjunction with external beam radiotherapy or as monotherapy. However, 192 Ir HDR brachytherapy is usually used to deliver a boost to external beam radiotherapy while 125 I seed implants are more commonly used as single modality treatment, restricting its application to early stage prostate cancer. It is notable that different groups in India are working on both these techniques and dosimetry., With the technological advancement in ultrasound equipment, fixing devices, US probe carriers, treatment planning systems and the availability of a variety of source configurations, brachytherapy is the choice of many physicians and even more importantly patients.
However, the success of any chosen modality depends upon accurate patient selection using, PSA level, Gleason Score, pathological staging and Partin's Table.
Initial trials of implanting radioactive seeds of 125 I through open retropubic route had resulted in poor results in localised prostate cancer. Transperineal percutaneous implants were introduced by Kumar for 125 I seeds and by Miller for 192 Ir wire. Since then the transperineal approach with trans-rectal ultrasound guidance has vastly improved the results. In the late 1980s Martinez in USA and Bertermann in the Netherlands started to use the same technique for HDR brachytherapy with 192 Ir source. Currently HDR monotherapy and seed implants with 125 I, 103 Pd and 131 Cs are extensively used in management of prostate cancer.
There are extensive discussions on the merits and demerits of seed implant therapy and HDR monotherapy. It is generally accepted that seed implant will not be suitable for prostate of volume more than 40 cm and for clinical staging beyond T2b, whereas prostate of larger volumes and staging up to T3c can be treated with HDR monotherapy. Another restriction in seed therapy is the interference of the pubic arch, which does not allow the placing of the seeds beyond the arch. It is also generally accepted that seeds should not be implanted in patients who had TURP done less than 6 months prior.
The single stepping source with variable dwell times used in HDR monotherapy has the greater potential of creating an optimised treatment plan after placement of the needles. Further, any needle movements could be accounted for in modifying the plan before subsequent fractions. However with seed implants seed migration might be a problem seed migration within the prostate and its periphery, both of which alter the planned dose distribution. There have been reports of seeds embolized in lung., This problem has been greatly reduced with the use RAPID Strands® and similar approaches where multiple seeds are embedded in a plastic strand reducing the risk of movement. RAPID Strand® also has helped improve the target coverage compared to use of individual seeds as seed implantation without migration outside of the prostate capsule is possible.
Currently in the management of prostate cancer the whole prostate with any extracapsular extension is treated though mostly the cancer is confined to the peripheral zones. Hence the prescription is typically to a minimum peripheral dose on the target volume for both techniques. The dose is 145 Gy for 125 I seed implants and 115 Gy for 103 Pd seed implants as per the recommendations of the American Association of Physicists in Medicine (AAPM) task group (TG 43) and guidelines of the American Brachytherapy Society (ABS)., However, no such recommendations exist for HDR brachytherapy yet. The number of HDR fractions and the fraction sizes are still debatable and vary widely from institution to institution. Clinical trials by various groups employ various fraction schedules. The William Beaumont group employs a total dose of 38 Gy delivered in four fractions over two days. The Osaka group uses 48 Gy in 8 fractions or 54 Gy in nine fractions, with two fractions per day. In dose escalation studies, Martinez and colleagues have used two fractions with 11.5 Gy per fraction. Most fractionation schedules are worked out to give an effective dose of more than 90 Gy @ 2 Gy fractions with the assumption that the a/b ratio is about 2.3 and the repair half time is 1.5 h. These values are still being debated as to their validity for irradiation with low dose rate for months compared to multiple fractions at high dose rate delivered within a couple of days. However it is generally accepted that prostate cancer with an a/b ratio less than 3 is more responsive to hypofractionated HDR treatment.
The dosimetry of seed implants may be a little questionable. Generally a preplan is generated based on ultrasound volume study performed 3-4 weeks prior to the implant. The DVH for D 90 (the dose delivered to 90% of the target volume) 30 days after the implant, is the golden parameter. It is assumed that by then the swelling of the gland due to the trauma of the implant has ceded and no more seed movement will take place. However since only about 30% of the prescription dose is delivered by 30th day (for 125 I implants) and the possibility of seed movements still later, it is surprising that the D 90 on Day 30 is accepted as a standard for the implant. Worse still, if one assumes that prostate cancer is slow growing, theoretically the delivery of the prescription dose over about 10 months, as with 125 I and 103 Pd may have an adverse effect on tumor control since the dose rate falls well below 0.2Gy per day, the sterilizing dose for slow growing tumors.
However, there is no doubt that considerable clinical experience has accumulated within the last 15 years with 125 I seed therapy whereas 103 Pd or 131 Cs seed therapy is relatively new. On the other side it is only within the last 5 years that HDR monotherapy has been initiated. Hence it is still too early for a comparison of clinical outcomes. Both the techniques are similar with regards to the use of trans rectal ultrasound. However with post implant dosimetry and optimization methods with a single source, HDR dosimetry is more flexible and accurate. Battermann and colleagues have summarised the clinical results of 125 I seed implant. With a mean follow-up of 50 months
(24-123 months) of 351 patients, they report an actuarial survival of 85% at 5 years and 76% at 7 years while actuarial bNED estimated freedom at 5 years was 64% and at 7 years 51%. With HDR monotherapy, a 3-year local control, overall survival and PSA failure free rates have been reported as 100, 97 and 83% with 111 patients with a media FU of 27 months, range 5-119 months. The corresponding 5 year rates are 97, 92 and 70%. A randomized prospective trial with a head to head comparison is still outstanding.
But local control is not the whole story. Generally the urinary complications reported are higher with seed implants. Grills reported decreased acute rates of grade 1-3 dysuria with HDR monotherapy (36%) against 67% ( P <0.001) for 103 Pd seed implant.. They also noted a reduction in urinary frequency 92% vs . 54% for HDR and LDR techniques ( P <0.001). Though urethral stricture of 8% was reported for the HDR group against 3% for LDR group ( P =0.177), 3-year actuarial impotence rate was only 16% in the HDR group, against 45% for the LDR group. The clinical results cannot be reliably compared as the HDR patients are generally in the higher risk group with increased PSA and advanced staging.
Finally, considerations must be given to resource requirements. Once the HDR unit is installed, the total cost including source changes can be shared with all HDR treatments. However, the cost of seeds varying in number from 80 to 120, will have to be charged to individual patients. Financial studies have shown that if more than 20-30 patients are treated annually, HDR monotherapy is more economical than seed therapy. Since the HDR treatments are given only in appropriately shielded rooms the patient does not harbour any radioactivity outside the room. However, with permanent implants, the seeds are left in the patient allowing to decay with their inherent half-life. Though the dose levels around the patient are low, this may still be of concern for children and pregnant women at home. When comparing these two modalities, the clinical outcome depends upon the selection of patients, conformal dosimetry, correct fractionation and total dose, local control, toxicities, patient comfort and acceptability and cost. A comparison of these parameters is given in [Table - 1].
In conclusion, HDR brachytherapy for prostate cancer can be delivered more conformally and safely with reduction in overall cost. Patients tolerate the technique very well. Results of long-term follow-up need to be awaited, however, one can expect them to be quite favorable for this modality. In fact, the trend in USA indicates an increased rate in the use of HDR brachytherapy relative to seed implants (Nissar Syed, Personal communication 2006).
| References|| |
|1.||Ravindran P, Lewis C, Van Dyk J, D'Souza D. Intraoperative dosimetry of trans-rectal ultrasound guided 125I prostate implants using fluoroscopic images. J Med Phys 2006;31:61-6. |
|2.||Jamena SV, Saju S, Shetty UM, Pallad S, Deshpande DD, Shrivastava SK. Dosimetric comparison of inverse optimization in combination with graphical optimization for HDR prostatic implants. J Med Phys 2006;31:89-94. |
|3.||Battermann JJ, Boon TA, de Voogt HJ. Preliminary results with iodine-125 seeds for permanent implantation in patients with localized prostatic cancer. Radiother Oncol 1987;10:91-5. [PUBMED] |
|4.||Kumar PP, Bartone FF. Transperineal percutaneous I-125 implant of the prostate. Urology 1980;17:238-40. |
|5.||Miller LS. After-loading transperineal iridium-192 wire implantation of the prostate. Radiology 1979;131:527-8. [PUBMED] |
|6.||Vicini FA, Horwitz EM, Kini VR, Stromberg JS, Martinez AA. Radiotherapy options for localized prostate cancer based upon pretreatment serum prostate-specific antigen levels and biochemical control: A comprehensive review of the literature. Int J Radiat Oncol Biol Phys 1998;40:1101-10. [PUBMED] [FULLTEXT]|
|7.|| Eshleman JS, Davis BJ, Pisansky TM, Wilson TM, Haddock MG, King BF, et al . Radioactive seed migration to the chest after transperineal interstitial prostate brachytherapy: Extraprostatic seed placement correlates with migration. Int J Radiat Oncol Biol Phys 2004;59:419-25. |
|8.||Nag S, Vivekanandam S, Martinez-Monge R. Pulmonary embolization of permanently implanted radioactive palladium-103 seeds for carcinoma of the prostate. Int J Radiat Oncol Biol Phys 1997 ; 39:667-70. |
|9.||Ankem MK, DeCarvalho VS, Harangozo AM, Hartanto VH, Perrotti M, Han K, et al . Implications of radioactive seed migration to the lungs after prostate brachytherapy. Urology 2002;59:555-9. |
|10.||Spadinger I, Hilts M, Keyes M, Smith C, Sidhu S, Morris WJ. Prostate brachytherapy post implant dosimetry: A comparison of suture-embedded and loose seed implants. Brachytherapy 2006;5:165-73. |
|11.||Battermann JJ. I-125 implantation for localized prostate cancer: The Utrecht University experience. Radiother Oncol 2000;57:269-72. [PUBMED] [FULLTEXT]|
|12.||Nath R, Anderson LL, Luxton G, Weaver KA, Williamson JF, Meigooni AS. Dosimetry of interstitial brachytherapy sources: Recommendations of the AAPM Radiation Therapy Committee Task Group No. 43. American Association of Physicists in Medicine. Med Phys 1995;22:209-34. |
|13.||Nag S, Beyer D, Friedland J, Grimm P, Nath R. American Brachytherapy Society (ABS) recommendations for transperineal permanent brachytherapy of prostate cancer. Int J Radiat Oncol Biol Phys 1999,44:789-99. |
|14.||Grills IS, Martinez AA, Hollander M, Huang R, Goldman K, Chen PY, et al . High dose rate brachytherapy as prostate cancer monotherapy reduces toxicity compared to low dose rate palladium seeds. J Urol 2004;171:1098-104. |
|15.||Yoshioka Y, Konishi K, Oh RJ, Sumida I, Yamazaki H, Nakamura S, et al . High-dose-rate brachytherapy without external beam irradiation for locally advanced prostate cancer. Radiother Oncol 2006;80:62-8. |
|16.||Martinez AA, Gustafson G, Gonzalez J, Armour E, Mitchell C, Edmundson G, et al . Dose escalation using conformal high-dose-rate brachytherapy improves outcome in unfavourable prostate cancer. Int J Radiat Oncol Biol Phys 2002;53:316-27. |
|17.||Bentzen SM, Ritter MA. The a/b ratio for prostate cancer: What is it, really? Radiat Oncol 2005;76:1-3. [PUBMED] [FULLTEXT]|
|18.||Duchesne GM, Peters LJ. What is alpha/beta ratio for prostatecancer? Rationale for hypofractionated high dose rate brachytherapy. Int J Radiat Oncol Biol Phys 1999;44:747-8. |
|19.||Martinez AA, Gustafson G, Gonzalez J, Armour E, Mitchell C, Edmundson G, et al . Dose escalation using conformal high-dose-rate brachytherapy improves outcome in unfavourable prostate cancer. Int J Radiat Oncol Biol Phys 2002,53:316-27. |
|20.||Dale RG. Radiobiological assessment of permanent implants using tumour repopulation factors in the linear-quadratic model. Br J Radiol 1989;62:241-4. [PUBMED] |
|21.||Battermann JJ, Boon TA, Moerland MA. Radiat Oncol 2004;71:23-8. |
|22.||Cosset JM, Haie-Meder C. Brachytherapy for prostate cancer: High dose rate or low dose rate? Cancer Radiother 2005;9:610-9. [PUBMED] [FULLTEXT]|
[Table - 1]