- Open Access
A comparison of dosimetric parameters between tomotherapy and three-dimensional conformal radiotherapy in rectal cancer
Radiation Oncologyvolume 8, Article number: 181 (2013)
Tomotherapy for intensity-modulated radiation has been demonstrated to reduce unnecessary irradiations to adjacent organs at risk (OARs). The purpose of this study was to compare the dosimetric parameters between Tomotherapy and three-dimensional conformal radiotherapy (3D-CRT) in rectal cancer patients.
Materials and methods
We redesigned three-dimensional conformal plans for 20 rectal cancer patients who had received short-course preoperative radiotherapy with Tomotherapy. The target coverage for 3D-CRT and Tomotherapy was evaluated with the following including the mean dose, VnGy, Dmin, Dmax, radiation conformality index (RCI), and radical dose homogeneity index (rDHI).
The mean PTV dose for Tomotherapy is significantly higher than that observed for the 3D-CRT (p = 0.043). However, there is no significant difference in the V23.25Gy, V26.25Gy, V27.5Gy, and RCI values between Tomotherapy and 3D-CRT. However, the average rDHI (p < 0.001) value for Tomotherapy was significantly lower than that reported for the 3D-CRT. Tomotherapy significantly lowered the mean level of irradiation doses to the bladder, small bowel, and femur heads as compared to 3D-CRT.
Tomotherapy could produce a favorable target coverage and significant dose reduction for the OARs at the expense of acceptable dose inhomogeneity of the PTV compared with 3D-CRT in rectal cancer patients.
According to the Korean National Cancer Screening Survey, the incidence of colorectal cancer has been increasing gradually in Korea. In addition, colorectal cancer is the third most common diagnosed malignancy, with an estimated 22,000 new cases per year . Conventional treatment with fractionated radiation of 50.4 Gy per 28 fractions for six weeks is a standard regimen that has been widely accepted for positive therapeutic outcomes of locally advanced rectal cancer, which is based on results from prospective randomized trials [2, 3]. Compared with postoperative radiotherapy, preoperative radiotherapy demonstrated an improvement in locoregional tumor control and resectability . In European countries, a short-course radiation treatment regimen of 25 Gy per five fractions for a week has frequently been used due to the decreased expense and increased convenience of a five-day irradiation for rectal cancer patients as compared to a five-week schedule of conventionally fractionated irradiation [4, 5]. A prospective randomized study has proven that there were no significant differences in survival and local tumor control between conventionally fractionated and short-course irradiation for locally advanced rectal cancer patients . However, there have been several reports that short-course irradiation has negative side effects including the increased risk of late small bowel obstruction, necessitating hospital admission, and sexual dysfunction [7, 8]. Therefore, clinicians have made considerable efforts to minimize the dose of irradiation to adjacent organs at risk (OARs) including the small bowel and bladder to avoid the long-term toxicity observed in rectal cancer patients.
Recently, techniques to improve the accuracy of radiation delivery to the target have advanced dramatically. Helical Tomotherapy (Accuary Inc., Sunnyvale, CA) which can involve image-guided radiation therapy using a megavoltage CT scan just prior to radiation treatment is one specific example of these advancements. Tomotherapy can also yield intensity-modulated radiation therapy (IMRT), which allows for highly conformal distributions of the dose of radiation to the target and minimizes the irradiation to the adjacent dose-limiting organs. Use of the IMRT technique to decrease an unnecessary irradiation to the bowel has been widely reported for the treatment of gynecologic cancers . However, dosimetric studies comparing IMRT and three-dimensional conformal radiation therapy (3D-CRT) in rectal cancer patients are scarce and assessed only in a small series . Thus, we compared the dosimetric parameters between Tomotherapy and 3D-CRT in rectal cancer patients who received preoperative radiotherapy.
Patients and simulation
Twenty consecutive patients with rectal cancer who had received short-course preoperative radiotherapy at Seoul St. Mary’s Hospital, Seoul, Korea from July 2010 to May 2011 were evaluated for the present study. They had locally advanced resectable disease (cT3 or cT4) with the inferior tumor margin located no further than 8 cm from the anal verge. The study participants included 14 men and 6 women, with a median age of 61 years (range, 39–77 years). This study was approved by the institutional review board of the Catholic University of Korea (KC10EIMS0025).
During treatment, patients were immobilized in the prone position using a foam cushion which covered the whole body. A contrast-enhanced CT was scanned for the treatment plan. Patients were instructed to have an empty bladder before the planning CT scan. The CT imaging ranged from the L1 vertebral body to 5 cm below the perineum, and axial images were obtained at 3-mm thickness and imported to the Pinnacle3 treatment planning system (Philips Radiation Oncology Systems, Fitchburg, WI).
Target volumes were defined according to the recommendation of the ICRU report 62 . The clinical target volume included the gross tumor volume and the presacral, mesorectal, common and internal iliac lymph nodes. The planning target volume (PTV) was symmetrically generated with 3 to 5-mm margins around the clinical target volume. The OARs such as bladder, small bowel, and femur heads were contoured. The small bowel was outlined 3 cm above and below the PTV, and the bladder and femur heads were fully outlined.
For the IMRT plan with Tomotherapy, the raw dosimetric data set of each patient was transferred from the Pinnacle3 treatment planning system to the Tomotherapy work-station (Figure 1A). For the 3D-CRT plan, a three-field technique (one anterior portal and two bilateral portals with wedge) was used (Figure 1B). Twenty-five Gy in five fractions delivered with 6 to 15 MV photon was prescribed for the PTV. Dose constraints for the PTV were as follows; (1) ≥ 98% of the PTV receives ≥ 95% of the prescribed dose, (2) ≤ 10% of the PTV receives ≥ 105% of the prescribed dose, (3) ≤ 5% of the PTV receives ≥ 110% of the prescribed dose. (4) None of the PTV receives ≥ 115% of the prescribed dose. No specific dose constraints for the OARs were used.
Dosimetric parameters to analyze target coverage and dose distribution in the PTV are as follows; (1) mean dose, (2) VnGy, percentage of the volume receiving radiation ≥ n Gy, (3) Dmin, minimum dose irradiated to the PTV, (4) Dmax, maximum dose irradiated to the PTV, (5) Radiation conformality index (RCI), PTV / V95% (volume enclosed by the 95% of isodose line), and (6) Radical dose homogeneity index (rDHI): Dmin / Dmax in the PTV. The avoidance of irradiation to the bladder, small bowel, and femur heads was evaluated using the values such as mean dose and VnGy.
The dosimetric parameters of Tomotherapy and 3D-CRT were compared using the t-test and the difference was considered statistically significant at the p < 0.05 level.
Written informed consent was obtained from the patient for publication of this report and any accompanying images.
Dose distribution of the planning target volume (PTV)
The median of the PTV outlined in the 20 patients was 1076 cc (range, 796 to 1435 cc). The Tomotherapy and 3D-CRT plan met the prescription requirements for the PTV in all cases. Dose parameters for the PTV in the Tomtherapy and 3D-CRT plan were listed and compared in Table 1. The mean PTV dose for Tomotherapy is significantly higher than that for the 3D-CRT (25.58 ± 0.35 vs. 25.19 ± 0.74 Gy, p = 0.043). However, there were no significant differences in the V23.25Gy, V26.25Gy, and V27.5Gy values between the Tomotherapy and 3D-CRT. Average Dmax values for the Tomotherapy and 3D-CRT were not significantly different. However, the average Dmin value for the Tomotherpay was significantly lower than that for the 3D-CRT (17.97 ± 1.93 vs. 22.05 ± 2.76 Gy, p < 0.001), and average rDHI value for the Tomotherapy is significantly lower than that for the 3D-CRT plan (0.70 ± 0.01 vs. 0.83 ± 0.04, p < 0.001). The average RCI values for the Tomotherapy and 3D-CRT were 1.01 and 1.00, respectively, and there is no significant difference in the average RCI value between the two modalities.
Avoidance of organs at risk (OARs)
Table 2 shows the mean irradiation doses of the OARs including the bladder, small bowel, and femur heads. The mean doses for the bladder, small bowel, and femur heads with the Tomotherapy were significantly lower than those reported for the 3D-CRT.
We investigated the dosimetric parameters of the small bowel, which is the most critical organ in the rectal cancer patients who received the preoperative pelvic irradiation. Table 3 summarizes the V25Gy, V22.5Gy, V20Gy, V17.5Gy , V15Gy, V10Gy, and V5Gy values of the small bowel with Tomotherapy and 3D-CRT. Tomotherapy produced significantly lower V25Gy, V22.5Gy, V20Gy, V17.5Gy , V15Gy, and V10Gy values for the small bowel as compared to the 3D-CRT. However, the V5Gy value, which reflected the low irradiation range of the normal tissue, was not significantly different between Tomotherapy and 3D-CRT (Figure 2).
IMRT modulates the beam intensity in several portals and has been demonstrated to achieve an effective coverage of the target tissue while avoiding damage to the normal tissue during treatment. Recently, IMRT has established an important role for the treatment of several malignancies through the promise of excellent local control of disease and reducing the potential complications inherent to external irradiation. Luxton G et al. reported that the accurate delivery of IMRT for prostate cancer could limit the dose to normal tissues and allow for a reduction in the rate of complication while maintaining the probability of tumor control . A report by Bazan JG et al. indicated that IMRT was associated with less gastrointestinal, dermatologic, and hematologic toxicities, reduced need for treatment breaks, and excellent tumor control, compared with 3D-CRT in patients with anal cancer . The National Comprehensive Consensus Network guidelines also recommend IMRT for the treatment of anal cancer patients in addition to 3D-CRT .
In rectal cancer patients, the preoperative short-course pelvic irradiation has demonstrated a definitive efficacy in reducing the local failure rate, compared with the rates reported for surgery alone [4, 5]. However, it has given rise to the incidence of late small bowel morbidities such as intestinal obstruction and chronic diarrhea that could alter the therapeutic ratio [7, 8]. Prognostic factors that increase the risk of late small bowel complications include extended fields out of the pelvis, irradiation dose, inappropriate irradiation technique, and increased small bowel irradiated volumes . The irradiation dose and volume of the small bowel in rectal cancer patients are of major concern to clinicians . Thus, we evaluated the dosimetric parameters of IMRT with Tomotherapy in rectal cancer patients. We hypothesized that Tomotherpay could reduce the overall dose to the normal tissue while maintaining the dose to the target, as compared to treatment with 3D-CRT.
In our study, the mean PTV dose for Tomotherapy is significantly higher than that for the 3D-CRT (25.58 ± 0.35 vs. 25.19 ± 0.74 Gy, p = 0.043) while Tomotherapy maintaining ≥ 98% of the PTV receives ≥ 95% of the prescribed dose and ≤ 10% of the PTV receives ≥ 105% of the prescribed dose. However, the rDHI for Tomotherapy is significantly lower than that for the 3D-CRT (0.70 ± 0.01 vs. 0.83 ± 0.04, p < 0.001) since the average Dmin value for the Tomotherpay was significantly lower than that for the 3D-CRT (17.97 ± 1.93 vs. 22.05 ± 2.76 Gy, p < 0.001). Local tumor control is related to the mean dose rather than to the minimum dose in the target . Moreover, a modest number of cold spots are not related to the reduced tumor control, and it is important to know the location and volume of the cold spots . When we have checked our Tomotherapy plans to identify the location of cold spots, they were very small and were predominantly located in the small bowel region adjacent to the PTV, which had a low probability of tumor involvement.
In our analysis, Tomotherapy significantly reduced the mean dose irradiated to the OARs such as bladder, small bowel, and femur heads as compared to 3D-CRT. Specifically, Tomotherapy significantly reduced the high to intermediate irradiation range (V25Gy, V22.5Gy, V20Gy, V17.5Gy, V15Gy, and V10Gy) to the small bowel compared to 3D-CRT. However, the V5Gy values which meant by low irradiation range of the radiation dose were similar between the Tomotherapy and 3D-CRT.
The result of the IMRT plans was associated with a trade-off between the coverage of the target and avoidance of the OSRs. We could attain optimal Tomotherapy plans, which significantly reduced the mean irradiation dose to the OARs at the expense of acceptable dose inhomogeneity of the PTV, because the goal of our IMRT plans was sparing of the OARs rather than full coverage of the target. Even though our study had inherent limitations including the retrospective nature and small patient number, our results support further investigation of IMRT for the treatment of rectal cancer patients [19–22].
In conclusion, our study shows that the use of Tomtherapy could produce favorable coverage for the target and decrease the mean dose for the OARs as compared to 3D-CRT for treatment of patients with rectal cancer. For a definitive conclusion, the Tomotherapy technique should be tested and compared with conventional radiation in a prospective series.
Lee EH, Lee HY, Choi KS, Jun JK, Park EC, Lee JS: Trends in cancer screening rates among Korean men and women: results from the Korean National Cancer Screening Survey (KNCSS), 2004–2010. Cancer Res Treat 2011,43(3):141-7. 10.4143/crt.2011.43.3.141
Sauer R, Becker H, Hohenberger W, Rödel C, Wittekind C, Fietkau R, et al.: Preoperative versus postoperative chemoradiotherapy for rectal cancer. N Engl J Med 2004,351(17):1731-1740. 10.1056/NEJMoa040694
Bosset JF, Collette L, Calais G, Mineur L, Maingon P, Radosevic-Jelic L, et al.: Chemotherapy with preoperative radiotherapy in rectal cancer. N Engl J Med 2006,355(11):1114-23. 10.1056/NEJMoa060829
Improved survival with preoperative radiotherapy in resectable rectal cancer. Swedish rectal cancer trial N Engl J Med 1997,336(14):980-987.
Kapiteijn E, Marijnen CAM, Nagtegaal ID, Putter H, Steup WH, Wiggers T, et al.: Preoperative radiotherapy combined with total mesorectal excision for resectable rectal cancer. N Engl JMed 2001,345(9):638-646. 10.1056/NEJMoa010580
Bujko K, Nowacki MP, Nasierowska-Guttmejer A, Michalski W, Bebenek M, Kryj M: Long-term results of a randomized trial comparing preoperative short-course radiotherapy with preoperative conventionally fractionated chemoradiation for rectal cancer. Br J Surg 2006,93(10):1215-23. 10.1002/bjs.5506
Birgisson H, Pahlman L, Gunnarsson U, Glimelius B: Late gastrointestinal disorders after rectal cancer surgery with and without preoperative radiation therap y . Br J Surg 2008,95(2):206-13.
Marijnen CA, van de Velde CJ, Putter H, van den Brink M, Maas CP, Martijn H, et al.: Impact of short-term preoperative radiotherapy on health-related quality of life and sexual functioning in primary rectal cancer: report of a multicenter randomized trial. J Clin Oncol 2005,23(9):1847-58. 10.1200/JCO.2005.05.256
Heron DE, Gerszten K, Selvaraj RN, King GC, Sonnik D, Gallion H, et al.: Conventional 3D conformal versus intensity-modulated radiotherapy for the adjuvant treatment of gynecologic malignancies: a comparative dosimetric study of dose-volume histograms small star, filled. Gynecol Oncol 2003,91(1):39-45. 10.1016/S0090-8258(03)00461-X
Arbea L, Ramos LI, Martínez-Monge R, Moreno M, Aristu J: Intensity-modulated radiation therapy (IMRT) vs. 3D conformal radiotherapy (3DCRT) in locally advanced rectal cancer (LARC): dosimetric comparison and clinical implications. Radiat Oncol 2010, 5: 17. 10.1186/1748-717X-5-17
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. 2010
Luxton G, Hancock SL, Boyer AL: Dosimetry and radiobiologic model comparison of IMRT and 3D conformal radiotherapy in treatment of carcinoma of the prostate. Int J Radiat Oncol Biol Phys 2004,59(1):267-284. 10.1016/j.ijrobp.2004.01.024
Bazan JG, Hara W, Hsu A, Kunz PA, Ford J, Fisher GA, et al.: Intensity-modulated radiation therapy versus conventional radiation therapy for squamous cell carcinoma of the anal canal. Cancer 2011,117(15):3342-51. 10.1002/cncr.25901
National Comprehensive Cancer Network (NCCN) clinical practice guidelines in oncology: anal cancer. NCCN ANAL-B 2011.
Bosset JF, Meneveau N, Pavy JJ: Late intestinal complications of adjuvant radiotherapy of rectal cancers. Cancer Radiother 1997,1(16):770-4.
Lee JH, Lee JH, Jang HS, Lee HC, Lee JW, Kang DG, et al.: Hypofractionated radiotherapy with tomotherapy for patients with hepatic oligometastases: retrospective analysis of two institutions. Clin Exp Metastasis 2013,30(5):643-50. 10.1007/s10585-013-9568-7
Nuyttens JJ, Robertson JM, Yan D, Martinez A: The variability of the clinical target volume for rectal cancer due to internal organ motion during adjuvant treatment. Int J Radiat Oncol Biol Phys 2002,53(2):497-503. 10.1016/S0360-3016(02)02753-0
Niemierko A, Goitein M: Implementation of a model for estimating tumor control probability for an inhomogeneously irradiated tumor. Radiother Oncol 1993,29(2):140-147. 10.1016/0167-8140(93)90239-5
Lee JH, Kim SH, Kim JG, Cho HM, Shim BY: Preoperative Chemoradiotherapy (CRT) followed by laparoscopic surgery for rectal cancer: predictors of the tumor response and the long-term oncologic outcomes. Int J Radiat Oncol Biol Phys 2011,81(2):431-8. 10.1016/j.ijrobp.2010.05.019
Lee JH, Jang HS, Kim JG, Cho HM, Shim BY, Oh ST, et al.: Lymphovascular invasion is a significant prognosticator in rectal cancer patients Who receive preoperative chemoradiotherapy followed by total mesorectal excision. Ann Surg Oncol 2012,19(4):1213-1221. 10.1245/s10434-011-2062-z
Lee JH, Kim DY, Nam TK, Yoon SC, Lee DS, Park JW, et al.: Long-term follow-up of preoperative pelvic radiotherapy and concomitant boost irradiation in locally advanced rectal cancer patients: a multi-institutional phase II study (KROG 04–01). Int J Radiat Oncol Biol Phys 2012,84(4):955-61. 10.1016/j.ijrobp.2012.01.045
Lee JH, Jo IY, Lee JH, Yoon SC, Kim YS, Choi BO, et al.: The role of postoperative pelvic radiation in stage IV rectal cancer after resection of primary tumor. Radiat Oncol J 2012,30(4):205-12. 10.3857/roj.2012.30.4.205
The authors wish to acknowledge the financial support of the Catholic Medical Center Research Foundation made in the program year of 2013 (5-2013-B0001-00050). Mina Yu and Joo Hwan Lee were equally contributed to this work.
All authors declare that they have no competing interests.
JHL: idea and concept. DMJ, JSC, and HSJ: design and development of Study. JHL, HCL, and HSJ: statistical analysis. JHL and MY: writing of manuscript and study coordinator. JHL and HSJ: final revision of manuscript. All authors read and approved the final manuscript.