RESEARCH ARTICLE | VOLUME 5, ISSUE 1 | OPEN ACCESS DOI: 10.23937/2378-3419/1410091

Which Has Better Dosimetry in Retroperitoneal Sarcoma: Rapid Arc or 3D Conformal Radiotherapy Techniques?

MW Hegazy1,2*, B Moftah3 and O Hassad3

1Section of Radiation Oncology, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia

2Department of Clinical Oncology & Nuclear Medicine, Zagazig College of Medicine, Egypt

3Department of Biomedical Physics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia

*Corresponding author: Mohamed W Hegazy, Section of Radiation Oncology, King Faisal Specialist Hospital & Research Center, KSA, PO Box 3354, Riyadh 11211 MBC 64, Saudi Arabia, Tel: +966-550-742-859.

Accepted: April 24, 2018 | Published: April 26, 2018

Citation: Hegazy MW, Moftah B, Hassad O (2018) Which Has Better Dosimetry in Retroperitoneal Sarcoma: Rapid Arc or 3D Conformal Radiotherapy Techniques?. Int J Cancer Clin Res 5:091.doi.org/10.23937/2378-3419/1410091

Copyright: © 2018 Hegazy MW, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Abstract


Aim

To compare which radiotherapy technique is better in retroperitoneal sarcoma (RPS) rapid Arc (RA) or 3D-Conformal Radiation Therapy (3D-CRT).

Methods and materials

Our study was on 10 patients with RPS diagnosed and treated at king Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia, planned for pre or postoperative radiation therapy with prescribed dose of 45Gy in 25 fractions. In both techniques, we looked at planning target volume (PTV) coverage, dose homogeneity and organs at risk dose (stomach, bowel, liver, kidneys and spinal cord).

Results

The PTV coverage, liver and stomach doses were similar in both plans however; RA significantly had better dose conformity (0.8 vs. 0.4, p = 0.034), dose homogeneity (1.08 vs. 1.3, p = 0.026), less bowel volume (V45 140cc vs. 243cc, p = 0.03) and lower Spinal cord dose (61% vs. 80%, p = 0.043).

Conclusion

Both plans achieved similar target coverage and organs at risk sparing however; RA showed statistically significant better dose homogeneity, bowel sparing volume and lower spinal cord dose in treating RPS by pre or postoperative radiation therapy.

Keywords


Retroperitoneal sarcoma, Pre or postoperative, Conformal, Rapid arc

Background


Retroperitoneal sarcoma (RPS) accounts to nearly 15% of all soft tissue sarcoma cases. The most common types are liposarcoma followed by leiomyosarcoma [1]. At time of presentation, RPS has a large size due to late diagnosis. The most common symptoms are vague abdominal pain, weight loss and anorexia. The liver and lungs may represent the most common sites of metastasis [2].

Surgery is the mainstay treatment of RPS, however achieving a gross total resection is critical [3-8]. The incidence of local recurrence is high, so radiation therapy has a potential important role for RPS. There is no answer to the better timing of radiation therapy either pre or postoperative. Pre and intraoperative radiation are done by Pawlik, et al. [9] and Gronchi, et al. [10] who added concurrent chemotherapy. Other studies applied the same regimen with encouraging RT results [11-13].

Aim


To compare which radiotherapy technique is better in RPS, RA or 3D-CRT.

Methods and Materials


Study design

Our study was on 10 patients with RPS diagnosed and treated at king Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia, 5 planned for preoperative and another 5 for postoperative radiation therapy with prescribed dose of 45Gy in 25 fractions. Dose constraints are shown in Table 1.

Table 1: Dose constraints. View Table 1

CT simulation and contouring

Planning CT scan was 4D performed with our departmental scanner (Philips Medical Systems, Cleveland, OH); with a slice thickness of 2 mm. Patients were placed supine with fully abducted arms with scanning from the upper thoracic to mid sacral spines. Fusion with preoperative CT, PET/CT or MRI scans was done to aid the delineation of gross target volume (GTV). GTV was expanded by 1.5 cm to create the clinical target volume (CTV), however in postoperative cases we have included the surgical clips as part of CTV then editing of organs at risk from CTV which then expanded by 1 cm to create the planning target volume (PTV). In both techniques, we looked at planning target volume coverage, dose homogeneity and organs at risk dose (stomach, bowel, liver, kidney, spinal cord).

Conventional 3D planning

Eclipse treatment planning system (Varian Medical Systems, Inc., Palo Alto, CA) was used along with the analytical anisotropic algorithm (AAA, Version 11.031) dose calculation algorithm. The plans were created with mixed 6 and 10 MV using 3-4 anterior, posterior and/or oblique fields.

Rapid arc

Eclipse treatment planning system was used with optimization using progressive resolution optimizer (PRO) Version11.031. All plans generated using True Beam linacs with 120 leaf millennium MLC and KV imaging, 2 arcs (full and/or partial), Arc mode, 6 and 10 MV. Arcs had the same isocenter at the center of the PTV.

Treatment plan evaluation

Dose-volume histogram statistics, dose conformity and dose homogeneity were analyzed to compare treatment plans. Both homogeneity (HI) [14-16] and conformity indices (CI) [17] were evaluated and calculated.

Statistical analysis

The planning target volumes, organs at risk, HI and CI endpoints were analyzed using non-parametric Wilcoxon signed rank test due to small sample size (SPSS, V19, USA), a probability value of < 0.05 considered to be statistically significant (two tailed).

Results


Target volume coverage

PTV coverage was achieved and comparable in both plans, (Table 2).

Table 2: Preoperative cases. View Table 2

Comparison of dosimetric parameters

The CI and HI of RA were better and statistically significant than 3D plan (CI 0.8 vs. 0.4, p = 0.034) and (HI 1.08 vs. 1.3, p = 0.026).

Normal tissue sparing

We analyzed the dose parameters (mean and maximum doses) of the liver, stomach and duodenum, kidneys, spinal cord and bowels (V45, mean and maximum doses) for all patients (Table 2). All parameters were comparable in both plans especially liver, stomach and duodenum, and bowel doses; however, RA has statistically significant less bowel volume (V45 140cc vs. 243cc, p = 0.03) and lower Spinal cord doses (mean 36% vs. 55% and maximum 61% vs. 80% with p value = 0.03 & 0.043 consequently) (Table 2, Table 3 and Table 4).

Table 3: Postoperative cases. View Table 3

Table 4: Statistical results. View Table 4

Discussion


The role of radiation therapy using both external beam and intraoperative radiation techniques for higher dose escalation to target volume either in naïve or recurrent RPS is still controversial with some studies achieved encouraging results [11-13,17-19]. Preoperative radiotherapy is preferred over postoperative one due to displacement of organs at risk especially bowel by the tumor itself with also better target coverage [20-22]. In our study we tried to look at which technique is better RA or 3D-CRT in RPS.

Using the same concept Paumier, et al. [23], Koshy, et al. [24] and Bossi, et al. [25] have been compared between 3D-CRT and IMRT of RPS, the first one [23] was for postoperative while the latter [24,25] was in the preoperative setting.

Regarding to the target coverage, it was identical in all the previous studies including our study except Koshy, et al. [24] who noticed increase of V95 (98.6% vs. 95.3%), PTV maximum and minimum doses (6% & 22%, P = 0.011 & P = 0.055) with IMRT arm.

Regarding to dose homogeneity, Paumier, et al. [23], Koshy, et al. [24] and Bossi, et al. [25] showed that CI was better in IMRT arm, similar to our results (CI 0.8 vs. 0.4, p = 0.034, HI 1.08 vs. 1.3, p = 0.026).

Regarding to organs at risk, Paumier, et al. [23] reported reduced bowel V50 and V40 five- and twofold, respectively with IMRT as in our study (V45 was 140cc vs. 243cc, p = 0.03), while Koshy, et al. [24] noted the lower small bowel volume receiving > 30Gy (63.5 to 43.1%, P = 0.043) with IMRT which was the same as by Bossi, et al. [25].

Paumier, et al. [23] reported the mean contralateral kidney dose increased from 1.5 (3D-CRT) to 4-4.4 Gy with IMRT, contrary to Bossi, et al. [25] who noticed that IMRT allows better sparing of the ipsilateral and contralateral kidney as well as in Koshy, et al. [24] while our results showed relative sparing of both kidneys by RA which was statistically insignificant, however bigger volume of the contralateral kidney received more doses in the RA arm.

Conclusion


Both plans achieved similar target coverage and organs at risk sparing however; RA showed statistically significant better dose homogeneity, dose conformity, bowel sparing volume and lower spinal cord dose in treating RPS by pre or postoperative radiation therapy.

Compliance with Ethical Standards


All authors declare that there is no conflict of interest. For retrospective review of data with less than minimal risk to the patients, no consent was required by the ethics committee.

References


  1. Tseng W, Martinez SR, Tamurian RM, Borys D, Canter RJ (2012) Histologic type predicts survival in patients with retroperitoneal soft tissue sarcoma. J Surg Res 172: 123-130.

  2. Lewis JJ, Leung D, Woodruff JM, MF Brennan (1998) Retroperitoneal soft-tissue sarcoma: Analysis of 500 patients treated and followed at a single institution. Ann Surg 228: 355-365.

  3. Anaya DA, Lahat G, Wang X, Xiao L, Tuvin D, et al. (2009) Establishing prognosis in retroperitoneal sarcoma: A new histology-based paradigm. Ann Surg Oncol 16: 667-675.

  4. Anaya DA, Lev DC, Pollock RE (2008) The role of surgical margin status in retroperitoneal sarcoma. J Surg Oncol 98: 607-610

  5. Lahat G, Anaya DA, Wang X, Tuvin D, Lev D, et al. (2008) Resectable well-differentiated versus dedifferentiated liposarcomas: Two different diseases possibly requiring different treatment approaches. Ann Surg Oncol 15: 1585-1593.

  6. Gronchi A, Lo Vullo S, Fiore M, Mussi C, Stacchiotti S, et al. (2009) Aggressive surgical policies in a retrospectively reviewed single-institution case series of retroperitoneal soft tissue sarcoma patients. J Clin Oncol 27: 24-30.

  7. Bonvalot S, Rivoire M, Castaing M, Stoeckle E, Le Cesne A, et al. (2009) Primary retroperitoneal sarcomas. A multivariate analysis of surgical factors associated with local control. J Clin Oncol 27: 31-37.

  8. Bonvalot S, Miceli R, Berselli M, Causeret S, Colombo C, et al. (2010) Aggressive surgery in retroperitoneal soft tissue sarcoma carried out at high-volume centers is safe and is associated with improved local control. Ann Surg Oncol 17: 1507-1514.

  9. Pawlik TM, Pisters PW, Mikula L, Feig BW, Hunt KK, et al. (2006) Long-term results of two prospective trials of preoperative external beam radiotherapy for localized intermediate- or high-grade retroperitoneal soft tissue sarcoma. Ann Surg Oncol 13: 508-517.

  10. Gronchi A, De Paoli A, Dani C, Merlo DF, Quagliuolo V, et al. (2014) Preoperative chemo-radiation therapy for localised retroperitoneal sarcoma: A phase I-II study from the Italian Sarcoma Group. Eur J Cancer 50: 784-792.

  11. Gieschen HL, Spiro IJ, Suit HD, Ott MJ, Rattner DW, et al. (2001) Long-term results of intraoperative electron beam radiotherapy for primary and recurrent retroperitoneal soft tissue sarcoma. Int J Radiat Oncol Biol Phys 50: 127-131.

  12. Petersen IA, Haddock MG, Donohue JH, Nagorney DM, Grill JP, et al. (2002) Use of intraoperative electron beam radiotherapy in the management of retroperitoneal soft tissue sarcomas. Int J Radiat Oncol Biol Phys 52: 469-475.

  13. Alektiar KM, Hu K, Anderson L, Brennan MF, Harrison LB, et al. (2000) High-dose-rate intraoperative radiation therapy (HDR-IORT) for retroperitoneal sarcomas. Int J Radiat Oncol Biol Phys 47: 157-163.

  14. Iori M, Cattaneo GM, Cagni E, Fiorino C, Borasi G, et al. (2008) Dose-volume and biological-model based comparison between helical tomotherapy and (inverse-planned) IMAT for prostate tumours. Radiother Oncol 88: 34-45.

  15. Whitelaw GL, Blasiak-Wal I, Cooke K, Usher C, Macdougall ND, et al. (2008) A dosimetric comparison between two intensity- modulated radiotherapy techniques: Tomotherapy vs dynamic linear accelerator. Br J Radiol 81: 333-340.

  16. Van't Riet A, Mak AC, Moerland MA, Elders LH, van der Zee (1997) A conformation number to quantify the degree of conformality in brachytherapy and external beam irradiation: Application to the prostate. Int J Radiat Oncol Biol Phys 37: 731-736.

  17. Sindelar WF, Kinsella TJ, Chen PW, DeLaney TF, Tepper JE, et al. (1993) Intraoperative radiotherapy in retroperitoneal sarcomas. Final results of a prospective, randomized, clinical trial. Arch Surg 128: 402-410.

  18. Gilbeau L, Kantor G, Stoeckle E, Lagarde P, Thomas L, et al. (2002) Surgical resection and radiotherapy for primary retroperitoneal soft tissue sarcoma. Radiother Oncol 65: 137-143.

  19. Trovik LH, Ovrebo K, Almquist M, Haugland HK, Rissler P, et al. (2014) Adjuvant radiotherapy in retroperitoneal sarcomas. A Scandinavian Sarcoma Group study of 97 patients. Acta Oncol 53: 1165-1172.

  20. Smith MJ, Ridgway PF, Catton CN, Cannell AJ, O'Sullivan B, et al. (2014) Combined management of retroperitoneal sarcoma with dose intensification radiotherapy and resection: Long-term results of a prospective trial. Radiother Oncol 110: 165-171.

  21. Nussbaum DP, Speicher PJ, Gulack BC, Ganapathi AM, Englum BR, et al. (2015) Long-term oncologic outcomes after neoadjuvant radiation therapy for retroperitoneal sarcomas. Ann Surg 262: 163-170.

  22. Nussbaum DP, Rushing CN, Lane WO, Cardona DM, Kirsch DG, et al. (2016) Preoperative or postoperative radiotherapy versus surgery alone for retroperitoneal sarcoma: A case-control, propensity score-matched analysis of a nationwide clinical oncology database. Lancet Oncol 17: 966-975.

  23. Paumier A, Le Pechoux C, Beaudre A, Negretti L, Ferreira I, et al. (2011) IMRT or conformal radiotherapy for adjuvant treatment of retroperitoneal sarcoma? Radiother Oncol 99: 73-78.

  24. Koshy M, Landry JC, Lawson JD, Esiashvili N, Staley CA, et al. (2003) Potential for toxicity reduction using intensity modulated radiation therapy (IMRT) for retroperitoneal sarcoma. Int J Radiat Oncol Biol Phys 57: S448-S449.

  25. Bossi A, De Wever I, Van Limbergen E, Vanstraelen B (2007) Intensity-modulated radiation therapy for preoperative posterior abdominal wall irradiation of retroperitoneal liposarcomas. Int J Radiat Oncol Biol Phys 67: 164-170.