Hostname: page-component-78c5997874-v9fdk Total loading time: 0 Render date: 2024-11-19T10:37:11.848Z Has data issue: false hasContentIssue false

Comparison of three-dimensional conformal irradiation techniques for prostate cancer using a low-energy (6 MV) photon beam

Published online by Cambridge University Press:  12 November 2010

Christina Armpilia*
Affiliation:
Department of Radiotherapy, Aretaieion Hospital, Medical School, University of Athens, 76 Vas Sophias av., 11528, Athens, Greece
Christos Antypas
Affiliation:
Department of Radiotherapy, Aretaieion Hospital, Medical School, University of Athens, 76 Vas Sophias av., 11528, Athens, Greece
Anna Zygogianni
Affiliation:
Department of Radiotherapy, Aretaieion Hospital, Medical School, University of Athens, 76 Vas Sophias av., 11528, Athens, Greece
Myrsini Balafouta
Affiliation:
Department of Radiotherapy, Aretaieion Hospital, Medical School, University of Athens, 76 Vas Sophias av., 11528, Athens, Greece
John Kouvaris
Affiliation:
Department of Radiotherapy, Aretaieion Hospital, Medical School, University of Athens, 76 Vas Sophias av., 11528, Athens, Greece
Panagiotis Sandilos
Affiliation:
Department of Radiotherapy, Aretaieion Hospital, Medical School, University of Athens, 76 Vas Sophias av., 11528, Athens, Greece
*
Correspondence to: Christina Armpilia, Department of Radiotherapy, Aretaieion Hospital, Medical School, University of Athens, 76 Vas Sophias av., 11528, Athens, Greece. E-mail: [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Purpose: To evaluate composite coplanar and non-coplanar three-dimensional conformal techniques (3D-CRT) for external-beam prostate radiotherapy using a low-energy (6 MV) photon beam.

Methods and Materials: For treatment-planning purposes, three different planning target volumes (PTV) were defined for ten patients with prostate cancer and as follows: PTV1 (pelvis), PTV2 (prostate + seminal vesicles + 1 cm margin) and PTV3 (prostate + 1 cm margin). Conformal techniques of 2, 3, 4, 5 (coplanar) and 6 (non-coplanar) field techniques have been considered and combined to produce five different plan combinations (i.e. techniques A, B, C, D and E). Treatment plans were generated with a prescription dose of 75 Gy to PTV3, 65 Gy to PTV2 and 45 Gy to PTV1 and were assessed on the basis of 3D dose distributions and dose-volume histograms (DVHs). Normal tissue-dose constraints for the relevant organs at risk (OARs), that is, rectum, bladder and femoral heads, were also considered.

Results: Findings show that all five treatment-plan combinations result in adequate PTV coverage and acceptable OAR irradiated volumes. The greatest rectal spacing in the high-dose region is achieved by technique C; all techniques achieve this, except for technique A, and give approximately the same fraction of volume (of rectum) that receives a dose of 50 Gy (V50) and 60 Gy (V60). When considering the bladder, techniques B, D and E give the best bladder sparing with small absolute differences, whereas technique A results in the lowest dose for femoral heads. Technique E appears to give the best compromise for all three considered OARs, provided the PTV is adequately covered.

Conclusions: Even though the optimum photon-beam energy for conformal prostate radiotherapy is greater than 10 MV, our study shows that a good sparing of OAR can be achieved even with a lower-energy beam (6 MV) and the appropriate plan combination and that the dose to prostate can be as high as 75 Gy.

Type
Original Article
Copyright
Copyright © Cambridge University Press 2010

INTRODUCTION

External beam radiation therapy is an effective treatment of localised and locally advanced stages of prostate cancer.Reference Geinitz, Zimmermann, Thamm, Schumertl, Bushch and Molls1,Reference Nguyen, Poortmans, van der Hulst, Studer, Pigois, Collen, Belkacemi, Beckendorf, Miralbell, Scandolaro, Soete, Villa, Gez, Thomas, Krengli and Jovenin2 In clinical practice, depending on the irradiation techniques and facilities, the need for high-radiation dose to be given to the tumour is often limited by the inevitable irradiation of the surrounding critical organs and the subsequent side-effects to them. Late side-effects are defined as those that develop and persist for more than 3 months after completion of treatment. In case of prostate radiation treatment, late rectal bleeding and bladder complications are more “dose-limiting” effects than acute effects because they are generally permanent and may be progressive in severity.Reference Hanks, Hanlon, Schultheiss, Pinover, Movsas, Epstein and Hunt3,Reference Dearnaley, Khoo, Norman, Meyer, Nahum, Tait, Yarnold and Horwich4 Toxicity of late effects depends on the volume of normal tissues irradiated.Reference Hanks, Hanlon, Schultheiss, Pinover, Movsas, Epstein and Hunt3,Reference Mesina, Sharma, Rissman, Geering, He and Forman5,Reference Pollack, Zagars, Starkschall, Childress, Kopplin, Boyer and Rosen6

Dose levels in the range of 65 Gy to 70 Gy have been proved to be effective for the external beam radiation therapy of locally advanced prostate cancer patients.Reference Pollack, Zagars, Starkschall, Childress, Kopplin, Boyer and Rosen6–Reference Zietman, DeSilvio, Slater, Rossi, Miller, Adams and Shipley10 However, studies with data from patients treated with conventional (non-3D) techniques (administered dose levels ≤70 Gy) have shown 7- to 10-year prostate-specific antigen (PSA) relapse-free survival rates of 65% in T1-T2 diseaseReference Shipley, Verhey, Munzenrider, Suit, Urie, McManus, Young, Shipley, Zietman and Biggs11 and 24% in more locally advanced T3 tumours.Reference Pollack, Zagars, Starkschall, Childress, Kopplin, Boyer and Rosen6,Reference Zagars, Eschenbach, Johnson and Oswald8,Reference Zietman, DeSilvio, Slater, Rossi, Miller, Adams and Shipley10 Higher doses have shown to improve the outcome, but rectal and bladder complications rates at 6.9%Reference Hanks, Hanlon, Schultheiss, Pinover, Movsas, Epstein and Hunt3,Reference Leibel, Heimann, Kutcher, Zelefsky, Burman, Melian, Orazem, Mohan, LoSasso and Lo12 have limited the ability to deliver higher doses with conventional techniques.

Three-dimensional conformal techniques (3D-CRT) are based on advanced 3D imaging and tumour visualisation techniques, 3D dose calculations algorithms and advanced beam-shaping technologies. The combined effect enables better conformation of dose distribution to the tumour area and improved sparing of critical organs. Safe administration of higher doses with lower rates of late side-effects may be achieved with 3D-CRT, compared to conventional RT. Several studies in the literatureReference Pollack, Zagars, Starkschall, Childress, Kopplin, Boyer and Rosen6,Reference Leibel, Heimann, Kutcher, Zelefsky, Burman, Melian, Orazem, Mohan, LoSasso and Lo12,Reference Sandler, McLaughlin, Ten Haken, Addison, Forman and Lichter13 have shown fewer acute toxic effects and an acceptable degree of late side-effects when the treatment dose to prostate cancer was increased from 65 Gy to 75 Gy or more. Other studiesReference Hanks, Hanlon, Schultheiss, Pinover, Movsas, Epstein and Hunt3,Reference Dearnaley, Khoo, Norman, Meyer, Nahum, Tait, Yarnold and Horwich4,Reference Zelefsky, Cowen, Fuks, Shike, Burman, Jackson, Venkatramen and Leibel14 indicate that a 10% increase in treatment dose may improve the local tumour control by 20% in radiosensitive tumours such as prostate. Intensity-modulated radiotherapy (IMRT) has been used to make possible more dose escalation – up to 85 Gy.Reference Pickett, Vigneault, Kurhanewicz, Verhey and Roach15,Reference Fraass, Kessler, McShan, Marsh, Watson, Dusseau, Eisbruch, Sandler and Lichter16 Although IMRT techniques offer more advantages in dose delivery compared to non-modulated 3D-CRT treatments, the latter remain a predominant method of treatment delivery for many radiotherapy centres around the world.

The optimum photon-beam energy used for 3D conformal prostate radiotherapy is greater than 10 MV. Beam arrangement in conformal techniques varies between centres. The choice of technique is often based on the departmental previous experience and on a preventive balancing of possible side-effects on the critical organs (rectum, bladder and femoral heads). A number of studies have been performed comparing different 3D coplanar and non-coplanar techniques used in prostate radiotherapy with differing results.Reference Khoo, Bedford, Webb and Dearnaley17–Reference Neal, Oldham and Dearnaley21

Our study was initiated mainly for the reason that many radiotherapy centres in our country are equipped with a single, low-energy (e.g. 6 MV), linear accelerator. The question that arises in such a case is, whether a radiotherapy department equipped with a single, low-energy linac is able to provide radical external-beam radiotherapy in prostate cancer patients or a high-energy linac is a prerequisite for such a treatment?

Therefore, the aim of the current study is to compare, in terms of final dose distribution and treatment-planning outcome and evaluation, different combinations of 3D conformal coplanar and non-coplanar techniques using a 6-MV linac beam. Radical radiotherapy of the prostate cancer with 3D-CRT techniques is considered adequate only if the given total dose to the prostate gland is at least 70 Gy; the main challenge for this study is whether or not a total dose of 75 Gy can be applied to the prostate while keeping the dose to the surrounding critical organs at levels considered safe.

METHODS AND MATERIALS

Ten randomly chosen patients with locally advanced prostate cancer histologically staged from T1c to T3b22 were retrospectively studied. All patients were aligned in supine position and marked for treatment positioning in the department’s simulator unit. Standard bilateral leg and knee immobilisation positioners were utilised for all patients. Prior to CT scan and treatment, all patients were advised to have full bladder and empty bowel. An axial CT scan of the pelvic region was used for treatment planning. Acquisition parameters were as follows: 120 kV tube voltage, 256 × 256 pixel matrix size, max 80 slices, 5 mm slice thickness, no interslice gap, field of view 250 × 250 mmReference Nguyen, Poortmans, van der Hulst, Studer, Pigois, Collen, Belkacemi, Beckendorf, Miralbell, Scandolaro, Soete, Villa, Gez, Thomas, Krengli and Jovenin2. CT images were DICOM imported into the Treatment Planning System (TPS; PLATO Sunrise™ v1.8, Nucletron Veenedal, Netherlands).

PTV and OAR contouring

Planning target volume (PTV) and the relevant organs at risk (OARs), that is, rectum, bladder and femoral heads, were contoured according to the recommendations of ICRU.23,24 Rectum was contoured from anal verge to recto-sigmoid flexure as a solid organ. Bladder was contoured as a whole organ, including the cavity.

The prostate gland was considered as the gross tumour volume (GTV), whereas three clinical target volumes (CTV) were identified for treatment planning purposes. CTV1 included the whole pelvis (prostate, bilateral seminal vesicles, internal iliac lymph nodes and inferior part of common iliac lymph nodes). CTV2 included the prostate, bilateral seminal vesicles, periprostatic tissues and all known areas of tumour extension. CTV3 included the prostate gland alone.

A 3D margin was added to define the corresponding PTVs – PTV1, PTV2 and PTV3 – to account for internal organ motion, patient movement and daily set-up errors. In all phases, except towards the rectum, where 0.5-cm margin was used, 1 cm was added isotropically from CTVi to PTVi.

Treatment techniques

Treatment was delivered in an ELEKTA SL-75-5 linear accelerator (Elekta Hellas EPE, Athens, Greece) with 6-MV photon beam. Treatment plans for each technique were generated in the PLATO TPS. Phase I prescription dose was 45 Gy to PTV1, phase II dose was 65 Gy to PTV2 and phase III dose was 75 Gy to PTV3. PTV contouring and respective phase doses are shown analytically in Table 1.

Table 1. CTV and PTV prescription doses

Five different combinations of treatment techniques have been considered in order to reveal the most efficient one in terms of overall dose distribution while keeping dose constraints to OARs. The considered planning-technique combinations are presented in Table 2. Analytically, in phase I, two techniques were considered: (1) 2-field (AP/PA) and (2) 4-field box. In phase II, three different techniques were considered: (1) 4-field box, (2) 3-field coplanar and (3) 5-field coplanar. In phase III, the 6-field non-coplanar technique was chosen for all combinations. This choice was made for the reason that, in phase III, the PTV3 is expected to be the smallest volume, compared to the PTV1 and PTV2. Moreover, this technique uses a larger number of beams aiming to better target conformity and greater sparing to OARs. In Figure 1 the observer’ eye view shows the patient body, the 3D PTV, and the rectum and the beam entries of the 6-field non-coplanar technique. Furthermore, 3D dose distributions were computed using a pencil-beam-based algorithm for the 6 MV photon beam. As the linac is not equipped with a multi-leaf collimator, custom-shaped blocks were used to conform the dose distribution to the PTV. Beam weights and wedge angles were adjusted to achieve dose homogeneity within the PTV, where the minimum requirement for dose homogeneity is defined in such measures as to23,24 allow for a 12% dose variation. Thus, coverage of the PTV was designed to be between -5% and +7% of the prescribed (isocentric) dose. To compare the plans, the dose distributions were normalised to the isocentre, and a reference dose equal to 95% of the isocentre dose was assessed.

Figure 1. Observer’s eye view (OEV) of the 6-field non-coplanar technique.

Table 2. 3D conformal treatment techniques

In accordance with minimum dose recommended in refs. 23 and 24, maximum dose and mean doses were recorded for the PTV and the OARs. Treatment plans were compared using 3D dose distributions and cumulative dose-volume histograms (cDVH).

Dose constraints to OARs

Dose constraints for the bladder, the rectum and the femoral heads were adopted using ICRU guidelines. Normal tissue limits (dose constraints) for plan generation are outlined in Table 3. The dose constraints for the OARs are assessed as figures of merit, in order to quantitatively compare the DVHs of the rectum, the bladder and the femoral heads.Reference Khoo, Bedford, Webb and Dearnaley17–Reference Fiorino, Reni, Cattaneo, Bolognesi and Calandrino19,Reference Emami, Lyman, Brown, Coia, Goitein, Munzenrider, Shank, Solin and Wesson25,Reference Kouloulias, Giraud, Davis, Dusserre, Zurlo and Bolla26

Table 3. Normal tissue dose constraints

(V70); fraction of the OAR volumes that receives a dose of 70 Gy.

RESULTS

Treatment plans were evaluated in terms of 3D-dose-distribution comparison and DVH values. Comparable results are summarised in Table 4, using mean statistics. Figures 2 and 3, respectively, illustrate comparisons between different DVH curves for rectum and bladder resulting from all the five techniques applied to a single patient. In Figures 4 and 5, a representative DVH (PTV and OARs) and dose distribution for technique E are presented respectively.

Table 4. Summary of DVH data for PTV and all OARs averaged over all ten patients for each of the five treatment-plan combinations

Mean (±1 SD) statistics are quoted.

V70: percentage of volume (%) irradiated to 70 Gy

Figure 2. Dose-volume histograms for rectum in a single patient for all five treatment-plan combinations.

Figure 3. Dose-volume histograms for bladder in a single patient for all five treatment-plan combinations.

Figure 4. Dose-volume histogram (PTV, rectum, bladder and fem heads) for technique E in a single patient.

Figure 5. Axial, sagittal and coronal dose distribution through the isocentre in a single patient for technique E. The isodoses (centre outwards) are 100, 95, 80 and 50% of the prescribed dose (75 Gy).

All five treatment-plan combinations satisfied normal tissue dose limits and resulted in adequate PTV coverage. In all cases, more than 95% of the PTV receives 95% of the prescribed dose (0.95 DPTV). The mean PTV were 1150 ± 162 cmReference Hanks, Hanlon, Schultheiss, Pinover, Movsas, Epstein and Hunt3 (phase I), 269 ± 94.2 cmReference Hanks, Hanlon, Schultheiss, Pinover, Movsas, Epstein and Hunt3 (phase II) and 149 ± 50.9 cmReference Hanks, Hanlon, Schultheiss, Pinover, Movsas, Epstein and Hunt3 (phase III), respectively.

In our study, as it can be seen in Table 4, all treatment techniques achieve the goal of rectal-dose constraint, that is, V70 < 30%. Among all techniques, technique C is giving the best rectal sparing, V70 = 21.5 ± 5.9% in the high-dose region. This is due to the relative higher weight of the lateral fields which better spare the rectum. In the lower-dose region, except for technique A all techniques present similar behaviour. In techniques B to E, V50 ranges from 64 to 67% and V60 ranges from 51 to 53% approximately, whereas in technique A the result was as follows: V50 = 98.5 ± 9.7%. It is evident that technique A and B deliver the highest dose to the rectum because they use a posterior field (180o) in all phases (I, II and III).

Regarding bladder sparing, technique A seems to give the best-possible V70 value (V70 = 34.5 ± 10.5%). However, when considering the comparative cDVHs in Figure 3, technique A elicited the poorest efficacy compared to all other techniques. In technique A, much greater volume of bladder receives dosages up to 60 Gy. For technique A, the proportion of the bladder receiving greater than 50 Gy (V50) of the isocentric dose was V50 = 90.2 ± 15.3%, whereas for all other techniques, it was V50 < 77%. Among techniques B, D and E, technique E gives the best bladder sparing: V50 = 75.5 ± 15.8 %. The higher SD values of bladder V70 and V50, corresponding to their respective rectum volumes, are due to the greater variation of bladder filling between patients.

In all cases, the whole femoral head dose does not exceed the 52-Gy threshold. It is evident (Table 4) that technique A, as it is the only technique that does not use lateral fields for phase I, gives the lowest mean dose, Dm = 27 Gy, to the entire femoral head. Techniques B to E give similar results, with technique E showing the best performance (Dm = 45 Gy).

DISCUSSION

Rectal toxicity appears to be the most clinical relevant and dose-limiting organ for prostate radiotherapy.Reference Michalski, Purdy, Winter, Roach, Vijayakumar, Sandler, Markoe, Ritter, Russell, Sailer, Harms, Perez, Wilder, Hanks and Cox9,Reference Lebesque, Bruce, Kroes, Touw, Shouman and van Herk27,Reference Jackson28 The probability of late rectal complications has been reported to increase with larger volumes irradiated to target dose levels. Reports in current literature concerning the radiation-induced toxicity to the rectum note that the percentage of rectal volume exposed to doses higher than 70 Gy is correlated with rectal bleeding.Reference Hanks, Hanlon, Schultheiss, Pinover, Movsas, Epstein and Hunt3,Reference Dearnaley, Khoo, Norman, Meyer, Nahum, Tait, Yarnold and Horwich4,Reference Pollack, Zagars, Starkschall, Childress, Kopplin, Boyer and Rosen6,Reference Zelefsky, Leibel, Gaudin, Kutcher, Fleshner, Venkatramen, Reuter, Fair, Ling and Fuks29,Reference Jackson, Skwarchuk, Zelefsky, Cowen, Venkatraman, Levegrun, Burman, Kutcher, Fuks, Liebel and Ling30 Several groups have investigated the risks of rectal toxicity on the basis of dose-volume assessments. For example, Zagars et al.Reference Zagars, Eschenbach, Johnson and Oswald8 noted a 3% incidence of major recto-sigmoid complications in patients receiving more than 70 Gy in rectal wall. Furthermore, Fiorino et al.Reference Fiorino, Reni, Cattaneo, Bolognesi and Calandrino19 noted that V50 below 60 to 65%, V60 below 45 to 50% and V70 below 25 to 30% should keep the rate of late bleeding (grades 2–3) between 5 and 10% for an ICRU dose between 70 and 78 Gy.

Regarding the use of non-coplanar treatment technique, reports in the literatureReference Bedford, Henrys, Dearnaley and Khoo20,Reference Neal, Oldham and Dearnaley21,,Reference Marsh, Ten Haken and Sandler31 suggest that such technique provides increase in rectal sparing—a finding which is also confirmed in our study. In fact, when comparing technique B, where all technique combinations are coplanar, with techniques C to E (in phase III, the non-coplanar technique is used) our data show that rectum V70 is reduced by 10 to 20%. In refs. 21,31 a technique involving left and right opposed fields together with two anterior inferior oblique fields is reported and was found to reduce the irradiated volume of rectum and bladder to a level comparable to that provided by opposed lateral fields alone. However, no consistent comparison of non-coplanar techniques has been mentioned in literature.

Bladder toxicity is not as common as rectal toxicity but can be a very late phenomenon, surfacing even several years after therapy. Predictors of late bladder injuries are more elusive due to the longer onset of injury and the more severe volume changes during therapy. The influence of the shape of the bladder on DVHs when considering the filling from one fraction to another is an important problem. This results in a more arbitrary determination of bladder dose constraints. Michalski et al.Reference Michalski, Purdy, Winter, Roach, Vijayakumar, Sandler, Markoe, Ritter, Russell, Sailer, Harms, Perez, Wilder, Hanks and Cox9 in 9406 RTOG trial for prostate cancer reported that the relative risk of developing acute or late bladder toxicity increased as the percentage of the bladder receiving more than 65 Gy increased. For doses more than 70 Gy Hanks et al.Reference Hanks, Leibel, Krall and Kramer7 and Lawton et al.Reference Lawton, Won, Pilepich, Asbell, Shipley, Hanks, Cox, Perez, Sause and Doggett32 observed a significantly increased incidence of grade 3 and grade 4 urinary toxicity. In general terms, fewer than 5% of patients develop chronic cystitis, but, occasionally, with doses higher than 75 Gy, approximately 5% of patients require cystectomy due to hemorrhagic cystitis.Reference Michalski, Purdy, Winter, Roach, Vijayakumar, Sandler, Markoe, Ritter, Russell, Sailer, Harms, Perez, Wilder, Hanks and Cox9 Our results are consistent with the reported bladder constraints as mean V70 was less than 40%.

When considering the femoral heads very little data are available on the dose–effect relationship. Using doses of approximately 60 to 64 Gy, a TD5/5 = 52 Gy for the entire femoral head has been suggested.Reference Khoo, Bedford, Webb and Dearnaley17,Reference Khoo, Bedford, Webb and Dearnaley18,Reference van Herk, Bruce, Kroes, Shouman, Touw and Lebesque33 In ref. 19 there is a suggestion from clinical experience that small fractions of femoral heads should tolerate relatively high doses (70 Gy). Thus, our data showing a maximum dose of 48.5 Gy to femoral heads (technique D) are consistent with the 52-Gy threshold mentioned in literature.

Overall, provided PTV is adequately covered, techniques B to E achieve the goal of dose constraints to the relevant OAR, whereas technique A proved to be the worst in bladder and rectum sparing in dosages approximately in the region of 40 Gy and 60 Gy (Figures 2 and 3). The influence of the shape and volume of the bladder and the rectum on DVHs becomes an important problem when considering the intrafraction filling and variation of both organs.Reference Mesina, Sharma, Rissman, Geering, He and Forman5,Reference Lebesque, Bruce, Kroes, Touw, Shouman and van Herk27,Reference Balter, Sandler, Lam, Bree, Lichter and ten Haken34 Controlling the filling of the bladder would result in significant improvement in the bladder sparing. Moreover, special diet could be advised to patients, in order that regular function of the rectum is maintained throughout the treatment course.

This study suggests that using 6-field non-coplanar treatment-planning techniques in phase III would result in better sparing of both the bladder and the rectum. These techniques are applied using a 6-MV linear accelerator without a multi-leaf collimator. Hence, the large number of beams associated with non-coplanar techniques increase the time taken to generate a plan, to produce custom-shaped blocks for each field and, finally, to deliver the treatment. All these lead to greater cost- and time-related constraints for patient. In routine use, technique B is more preferable to technique E for two reasons: (1) it satisfies adequately the pre-set planning constraints for all three OAR, and (2) it has the advantage of being less expensive in terms of preparation, execution and verification of the treatment.

It is clear that pelvic anatomy varies greatly from patient to patient; perhaps the best way to ensure an optimal treatment technique for a given patient is to evaluate a variety of plans, but this could delay planning.

CONCLUSIONS

In this study, five different combinations of 3D-conformal coplanar and non-coplanar techniques using a 6 MV linac beam have been compared. Provided that the PTV is adequately covered, the choice of the optimal plan arrangement for prostate cancer is always a compromise between dose to all three OAR—rectum, bladder and femoral heads. Although it is desirable to use photon beams of higher energy at 10 MV and higher for conformal prostate radiotherapy, our study shows that even with a lower-energy beam (6 MV) and the appropriate plan combination a good sparing of OAR can be achieved while the dose to prostate can be as high as 75 Gy.

References

Geinitz, H, Zimmermann, FB, Thamm, R, Schumertl, A, Bushch, R, Molls, M. 3D conformal radiation therapy for prostate cancer patients treated with radiotherapy. Int J Radiat Oncol Biol Phys 2005; 61:10111018Google Scholar
Nguyen, TD, Poortmans, PM, van der Hulst, M, Studer, G, Pigois, E, Collen, TD, Belkacemi, Y, Beckendorf, V, Miralbell, R, Scandolaro, L, Soete, G, Villa, S, Gez, E, Thomas, O, Krengli, M, Jovenin, N. The curative role of radiotherapy in adenocarcinoma of the prostate in patients under 55 years of age: a rare cancer network retrospective study. Radiother Oncol 2005; 77:286289.CrossRefGoogle ScholarPubMed
Hanks, GE, Hanlon, AL, Schultheiss, TE, Pinover, WH, Movsas, B, Epstein, BE, Hunt, MA. Dose escalation with 3D conformal treatment: five year outcomes, treatment optimization, and future directions. Int J Radiat Oncol Biol Phys 1998; 41:501510.CrossRefGoogle ScholarPubMed
Dearnaley, DP, Khoo, VS, Norman, AR, Meyer, L, Nahum, A, Tait, D, Yarnold, J, Horwich, A. Comparison of radiation side-effects of conformal and conventional radiotherapy in prostate cancer: a randomised trial. Lancet 1999; 353:267272.CrossRefGoogle ScholarPubMed
Mesina, CF, Sharma, R, Rissman, LS, Geering, L, He, T, Forman, JD. Comparison of a conformal nonaxial boost with a four-field boost technique in the treatment of adenocarcinoma of the prostate. Int J Radiat Oncol Biol Phys 1994; 30:427430.Google Scholar
Pollack, A, Zagars, GK, Starkschall, G, Childress, CH, Kopplin, S, Boyer, AL, Rosen, II. Conventional vs. conformal radiotherapy for prostate cancer: preliminary results of dosimetry and acute toxicity. Int J Radiat Oncol Biol Phys 1996; 34:555564.Google Scholar
Hanks, GE, Leibel, SA, Krall, JM, Kramer, S. Patterns of care studies: dose-response observations for local control of adenocarcinoma of the prostate. Int J Radiat Oncol Biol Phys 1985; 11:153157.CrossRefGoogle ScholarPubMed
Zagars, GK, von Eschenbach, AC, Johnson, DE, Oswald, MJ. Stage C adenocarcinoma of the prostate. An analysis of 551 patients treated with external beam radiation. Cancer 1987; 60:14891499.Google Scholar
Michalski, JM, Purdy, JA, Winter, K, Roach, M 3rd, Vijayakumar, S, Sandler, HM, Markoe, AM, Ritter, MA, Russell, KJ, Sailer, S, Harms, WB, Perez, CA, Wilder, RB, Hanks, GE, Cox, JD. Preliminary report of toxicity following 3D radiation therapy for prostate cancer on 3DOG/RTOG 9406. Int J Radiat Oncol Biol Phys 2000; 46:391402.Google Scholar
Zietman, AL, DeSilvio, ML, Slater, JD, Rossi, CJ Jr, Miller, DW, Adams, JA, Shipley, WU. Comparison of conventional-dose vs high-dose conformal radiation therapy in clinically localized adenocarcinoma of the prostate: a randomized controlled trial. JAMA 2005; 294:12331239.Google Scholar
Shipley, WU, Verhey, LJ, Munzenrider, JE, Suit, HD, Urie, MM, McManus, PL, Young, RH, Shipley, JW, Zietman, AL, Biggs, PJ. Advanced prostate cancer: the results of a randomized comparative trial of high dose irradiation boosting with conformal protons compared with conventional dose irradiation using photons alone. Int J Radiat Oncol Biol Phys 1995; 32:312.Google Scholar
Leibel, SA, Heimann, R, Kutcher, GJ, Zelefsky, MJ, Burman, CM, Melian, E, Orazem, JP, Mohan, R, LoSasso, TJ, Lo, YC. Three-dimensional conformal radiation therapy in locally advanced carcinoma of the prostate: preliminary results of a phase I dose-escalation study. Int J Radiat Oncol Biol Phys 1994; 28:5565.CrossRefGoogle ScholarPubMed
Sandler, HM, McLaughlin, PW, Ten Haken, RK, Addison, H, Forman, J, Lichter, A. Three dimensional conformal radiotherapy for the treatment of prostate cancer: low risk of chronic rectal morbidity observed in a large series of patients. Int J Radiat Oncol Biol Phys 1995; 33:797801.CrossRefGoogle Scholar
Zelefsky, MJ, Cowen, D, Fuks, Z, Shike, M, Burman, C, Jackson, A, Venkatramen, ES, Leibel, SA. Long term tolerance of high dose three-dimensional conformal radiotherapy in patients with localized prostate carcinoma. Cancer 1999; 85:24602468.3.0.CO;2-N>CrossRefGoogle ScholarPubMed
Pickett, B, Vigneault, E, Kurhanewicz, J, Verhey, L, Roach, M. Static field intensity modulation to treat a dominant intra-prostatic lesion to 90 Gy compared to seven field 3-dimensional radiotherapy. Int J Radiat Oncol Biol Phys 1999; 44:921929.CrossRefGoogle Scholar
Fraass, BA, Kessler, ML, McShan, DL, Marsh, LH, Watson, BA, Dusseau, WJ, Eisbruch, A, Sandler, HM, Lichter, AS. Optimization and clinical use of multisegment intensity-modulated radiation therapy for high-dose conformal therapy. Semin Radiat Oncol 1999; 9:6077.CrossRefGoogle ScholarPubMed
Khoo, VS, Bedford, JL, Webb, S, Dearnaley, DP. An evaluation of three-field coplanar plans for conformal radiotherapy of prostate cancer. Radiother Oncol 2000; 55:3140.CrossRefGoogle ScholarPubMed
Khoo, VS, Bedford, JL, Webb, S, Dearnaley, DP. Class solutions for conformal external beam prostate radiotherapy. Int J Radiat Oncol Biol Phys 2003; 55:11091120.CrossRefGoogle ScholarPubMed
Fiorino, C, Reni, M, Cattaneo, GM, Bolognesi, A, Calandrino, R. Comparing 3-, 4- and 6-fields techniques for conformal irradiation of prostate and seminal vesicles using dose-volume histograms. Radiother Oncol 1997; 44:251257.CrossRefGoogle ScholarPubMed
Bedford, JL, Henrys, AJ, Dearnaley, DP, Khoo, VS. Treatment planning evaluation of non-coplanar techniques for conformal radiotherapy of the prostate. Radiother Oncol 2005; 75:287292.CrossRefGoogle ScholarPubMed
Neal, AJ, Oldham, M, Dearnaley, DP. Comparison of treatment techniques for conformal radiotherapy of the prostate using dose-volume histograms and normal tissue complication probabilities. Radiother Oncol 1995; 37:2934.CrossRefGoogle ScholarPubMed
International Union Against Cancer (UICC). TNM classification of malignant tumours. 4th edn. Berlin, Heidelberg, New York: Springer-Verlag, 1999.Google Scholar
International Commission on Radiation Units and Measurements. Prescribing, recording and reporting photon beam therapy, ICRU report 50. Bethesda, MD: International Commission on Radiation Units and Measurements, 1993, pp. 3–16.Google Scholar
International Commission on Radiation Units and Measurements. Prescribing, recording and reporting photon beam therapy, ICRU report 62. Bethesda, MD: International Commission on Radiation Units and Measurements, 1999.Google Scholar
Emami, B, Lyman, J, Brown, A, Coia, L, Goitein, M, Munzenrider, JE, Shank, B, Solin, LJ, Wesson, M. Tolerance of normal tissue to therapeutic irradiation. Int J Radiat Oncol Biol Phys 1991; 21:109122.CrossRefGoogle ScholarPubMed
Kouloulias, VE, Giraud, JY, Davis, BJ, Dusserre, A, Zurlo, A, Bolla, M. Quality assurance of the 22961 EORTC trial. A phase III study of the optimal combination of hormonal adjuvant treatment by LHRH analogue and radiation therapy for the management of locally advanced prostate cancer: the dummy run. Radiother Oncol 2004; 73:1120.Google Scholar
Lebesque, JV, Bruce, AM, Kroes, AP, Touw, A, Shouman, RT, van Herk, M. Variation in volumes, dose-volume histograms, and estimated normal tissue complication probabilities of rectum and bladder during conformal radiotherapy of T3 prostate cancer. Int J Radiat Oncol Biol Phys 1995; 33:11091119.Google Scholar
Jackson, A. Partial irradiation of the rectum. Semin Radiat Oncol 2001; 11:215223.Google Scholar
Zelefsky, MJ, Leibel, SA, Gaudin, PB, Kutcher, GJ, Fleshner, NE, Venkatramen, ES, Reuter, VE, Fair, WR, Ling, CC, Fuks, Z. Dose escalation with three-dimensional conformal radiation therapy affects the outcome in prostate cancer. Int J Radiat Oncol Biol Phys 1998; 41:491500.Google Scholar
Jackson, A, Skwarchuk, MW, Zelefsky, MJ, Cowen, DM, Venkatraman, ES, Levegrun, S, Burman, CM, Kutcher, GJ, Fuks, Z, Liebel, SA, Ling, CC. Late rectal bleeding after conformal radiotherapy of prostate cancer. II. Volume effects and dose-volume histograms. Int J Radiat Oncol Biol Phys 2001; 49:685698.Google Scholar
Marsh, LH, Ten Haken, RK, Sandler, HM. A customized non-axial external beam technique for treatment of prostate carcinomas. Med Dosim 1992; 17:123127.CrossRefGoogle ScholarPubMed
Lawton, CA, Won, M, Pilepich, MV, Asbell, SO, Shipley, WU, Hanks, GE, Cox, JD, Perez, CA, Sause, WT, Doggett, SR. Long-term treatment sequelae following external beam irradiation for adenocarcinoma of the prostate: analysis of RTOG studies 7506 and 7706. Int J Radiat Oncol Biol Phys 1991; 21:935939.CrossRefGoogle ScholarPubMed
van Herk, M, Bruce, A, Kroes, AP, Shouman, T, Touw, A, Lebesque, JV. Quantification of organ motion during conformal radiotherapy of the prostate by three dimensional image registration. Int J Radiat Oncol Biol Phys 1995; 33:13111320.CrossRefGoogle ScholarPubMed
Balter, JM, Sandler, HM, Lam, K, Bree, RL, Lichter, AS, ten Haken, RK. Measurement of prostate movement over the course of routine radiotherapy using implanted markers. Int J Radiat Oncol Biol Phys 1995; 31:113118.Google Scholar
Figure 0

Table 1. CTV and PTV prescription doses

Figure 1

Figure 1. Observer’s eye view (OEV) of the 6-field non-coplanar technique.

Figure 2

Table 2. 3D conformal treatment techniques

Figure 3

Table 3. Normal tissue dose constraints

Figure 4

Table 4. Summary of DVH data for PTV and all OARs averaged over all ten patients for each of the five treatment-plan combinations

Figure 5

Figure 2. Dose-volume histograms for rectum in a single patient for all five treatment-plan combinations.

Figure 6

Figure 3. Dose-volume histograms for bladder in a single patient for all five treatment-plan combinations.

Figure 7

Figure 4. Dose-volume histogram (PTV, rectum, bladder and fem heads) for technique E in a single patient.

Figure 8

Figure 5. Axial, sagittal and coronal dose distribution through the isocentre in a single patient for technique E. The isodoses (centre outwards) are 100, 95, 80 and 50% of the prescribed dose (75 Gy).