Journal of Radiotherapy

Journal of Radiotherapy / 2014 / Article

Research Article | Open Access

Volume 2014 |Article ID 325057 | https://doi.org/10.1155/2014/325057

Siji Cyriac, M. M. Musthafa, R. Ganapathi Raman, K. Abdul Haneefa, V. T. Hridya, "Pretreatment Patient Specific Quality Assurance and Gamma Index Variation Study in Gantry Dependent EPID Positions for IMRT Prostate Treatments", Journal of Radiotherapy, vol. 2014, Article ID 325057, 5 pages, 2014. https://doi.org/10.1155/2014/325057

Pretreatment Patient Specific Quality Assurance and Gamma Index Variation Study in Gantry Dependent EPID Positions for IMRT Prostate Treatments

Academic Editor: Tibor Major
Received30 Nov 2013
Accepted29 Jan 2014
Published05 Mar 2014

Abstract

Pretreatment quality assurance (QA) is a major concern in complex radiation therapy treatment plans like intensity modulated radiation therapy (IMRT). Present study considers the variations in gamma index for gantry dependent pretreatment verification and commonly practiced zero gantry angle verifications for ten prostate IMRT plans using two commercial medical linear accelerators (Varian 2300 CD, Varian Clinac iX). Two verification plans (the one with all fields at the actual treatment angles and one with all fields merged to 0 degree gantry angles) for all the patients were generated to obtain dose fluence mapping using amorphous silicon electronic portal imaging device (EPID). The gamma index was found depend on gantry angles but the difference between zero and the nonzero treatment angles is in the confidence level for clinical acceptance. The acceptance criteria of gamma method were always satisfied in both cases for two machines and are stable enough to execute the patient specific pretreatment quality assurance at 0 degree gantry angle for prostate IMRTs, where limited number of gantry angles are used.

1. Introduction

Modern cancer treatments using radiation therapy is mostly employed with multileaf optimized plans as in intensity modulated radiation therapy. Higher monitor units and continuous motion of multi-leafs during the beam on time need to be strictly monitored for beneficial outcome from IMRT treatments. Complex IMRT plans are widely used in routine clinical practice which requires pretreatment patient specific quality assurance tests [1, 2]. Pretreatment quality assurance in complex treatment techniques like intensity modulated radiation therapy is carried out using electronic portal imaging devices attached to the medical linacs. This ensures the accuracy of treatment plan generated using commercial planning systems for complex IMRT treatments.

Pretreatment quality verification is advisable in all IMRT treatment plans to compare the beam fluence maps delivered using continuous motion of multileaf collimators (MLC). Most centers execute the patient specific verification plans generated prior to the first treatment fraction, where all the fields with various gantry angles are merged to zero degree gantry angle and dose fluence generated from TPS is cross-checked using EPID outputs [3, 4]. The linacs attached with EPID make the pretreatment QA easier and faster than other commercial tools like 2D detector arrays, which is time consuming for machinery settings. EPIDs provide high resolution two-dimensional data. It requires virtually no time for patient set-up or postprocessing to obtain useful data with a fast image acquisition which is stored in digital for further analysis [58].

Apart from usual zero degree gantry angles, many studies [9, 10] investigated the fluence matching in oblique angles. Gravitational sagging of linac head and EPID tail can influence the quality assurance [11, 12]. However, if the sagging is minimal, we can achieve the actual treatment delivery positions for pretreatment verification purpose. This helps us to get the actual dose mapping in EPIDs. The MLC motion and collimator rotations can be influenced by the gravity shifts in nonzero gantry angles. This will be more severe in IMRT treatments where the critical organs are closely covered using MLCs.

This work aims to compare IMRT pretreatment verification for prostate plans, from two commercial medical linac accelerator machines where on-board EPID (PortalVision, Varian Medical Systems, Palo Alto, CA) is available. Dose fluence mapping were performed using EPIDs, to compare with the TPS generated dose maps using gamma index technique (3 mm, 3%, integrated in Eclipse TPS) with two methods: one with actual treatment gantry angles and the other with all gantry angles merged to zero degree gantry angle.

2. Materials and Methods

Measurements were taken from two commercial medical linear accelerators—Varian Clinac 2300CD and Varian Clinac iX (Varian Associates, Palo Alto, CA). Clinac 2300 CD is equipped with 80 dynamic MLC and Clinac iX is equipped with Millennium 120 dynamic MLC. Both machines are fully commissioned for treating patients using IMRT technique. Both machines have 6 and 18 MV photon beams and onboard amorphous-silicon EPID (aS500-Varian Medical Systems, Palo Alto, CA). EPID can be positioned at all gantry angles by motorized robotic, three-axis extract arms [13].

Ten prostate IMRT plans were generated for our study with gantry angles; 0° (anterior), 75° (right anterior oblique), 135° (right posterior oblique), 225° (left posterior oblique), and 285° (left anterior oblique) using 6 MV photon energies as shown in Figure 1. Varian Eclipse v.n.11.0 treatment planning system (Varian Medical Systems, Palo Alto, CA) was used to create the plans, where analytical anisotropic analytical algorithm (AAA) [14] is available for the optimization. Target and critical organ delineations were performed by the same radiation oncologist and the same medical physicist who did the dosimetric optimizations in all plans. Our linacs are precalibrated with farmer ionization chamber (0.6 cm3 PTW 30001) and associated PTW Freiburg electrometer (PTW 10008), using TRS 398 Dw protocol [15].

As per the Atomic Energy Regulatory Board of India (AERB) [16] safety rules, the leaf positions are periodically checked and documented for both machines. A mechanical front pointer made up of steel is attached to linac head to determine the distance between the target and the surface of the EPID. Pin point maker was drawn in “standard graph” and pasted on EPID using the front pointer while the gantry is at zero degree angle. The deviations from the marked position in all (, , and ) directions are noted while the gantry is rotated. The measurements are noted for standard field size of 10 × 10 cm2 for 0°, 60°, 120°, 180°, and 240° gantry angles. These measurements will give the EPID and gantry deviation while gantry on rotation.

The MLC position checks are performed in different ways during the study. Standard shapes (say “”) are imported from TPS to linac and performed the reproducibility on EPID for various gantry angles. Monthly checks on MLC leaf position is to irradiate an imported (from TPS) image using radiographic films and is done on zero degree gantry angle. No significant sagging, dislocations, or misalignments in collimator leaf positions were noticed while rotation during this study. Leaf position accuracy is studied on both machines using radiographic films in limited gantry angles. The measurement result of radiographic film on zero degree gantry angle from Clinac 2300 CD is shown in Figure 4, where alternate MLC leafs from both sides are closed to generate compatible shape for MLC position accuracy study, projecting to the isocenter. These studies give the confidence on the MLC position accuracy and are essential to make sure any misalignments of multileafs are under threshold for clinical acceptance.

Two sets of verification plans were created, one with the actual gantry angle and the other with all fields merged to zero degree gantry angle. Varian medical system has dedicated portal dosimetry software and is embedded in our Eclipse planning system [17]. This software can compare the dose fluence map using gamma index [18] method. The treatment plans generated from TPS were compared with the EPID measured dose maps. In the low gradient regions; the mean difference in dose should not be greater than 3% of prescribed dose. On the same time, in high gradient region the distance to agreement should not be greater than 3 mm. This was the default and acceptable settings for all IMRT plans in our institute, which is followed in this study as well.

Gamma index pretreatment evaluations were performed for ten patients in two machines separately for actual treatment gantry angles and for the zero degree gantry angles. The criterion of acceptability of the gamma evaluation requires that no more than 5% of the points should have a gamma value larger than one. The percentage of points satisfying the above passing criteria was found by comparing the TPS generated 2D gamma map with EPID provided 2D gamma map in zero and at actual gantry angles. The percentage difference in acceptance criteria for each field (th) was calculated by subtracting the percentage obtained with actual gantry angles () from that obtained with zero degree gantry angle (). ROOT v5-34 [19] software was used to plot these values after dependent Student’s -test for statistical acceptance ().

3. Results and Discussion

EPID shifts were found in daily quality assurance checks, for 10 × 10 cm2 open square field projections at 0°, 60°, 120°, 180°, and 240° gantry angle positions. Maximum deviations in , , and shifts range from −1.2 mm to 0.95 mm, −0.75 mm to 0.68 mm, and −0.2 mm to 0.3 mm, respectively. All the pretreatment quality assurance was carried out after checking the EPID shifts. The shifts in all directions are taken into account and corrected for all fields.

Gamma index acceptance criteria were always satisfactory in both linear accelerators for both zero degree gantry and nonzero gantry angle pretreatment quality assurance tests. The difference in two values , one obtained with gantry at zero degree and the other with individualized gantry angles (0°, 75°, 135°, 225°, and 285°) for all ten patients for Clinac iX and Clinac 2300 CD, are as shown in Figures 2 and 3, respectively.

Both linacs have independent behavior in the gantry angle dependent pretreatment verifications. Maximum differences in gamma index values were obtained for Clinac iX machine. While for both the machines maximum difference in acceptance criteria was found in 135° and 225° gantry angles, the mean values of the percentage of the points having a gamma less than one for nonzero gantry angles in Clinac 2300 CD machine are % (75°), % (135°), % (225°), and % (285°) and for Clinac iX machine are % (75°), % (135°), % (225°), and % (285°). The mean value of the percentage that satisfies the gamma points passing criteria measured at zero degree for Clinac 2300 CD and Clinac iX was (%) and (%), respectively. The student’s -test value were found to be 0.02 (0.001 0.05) for all ten IMRT patients.

It is always advisable to check the gantry sagging effects for reasonable results from individualized gantry angle pretreatment quality assurance. This improves the IMRT quality and ensures the adequacy of the complex IMRT plans. Periodic mechanical quality assurance for gantry sagging using mechanical pointer attached to collimator must be carried out before IMRT treatments.

Besides the gantry sagging, MLC position accuracy must be studied independently to ensure the MLC position tolerance limits. During this study, collimator leaf position accuracy checks using light field on EPID surface for various gantry angles show negligible deviations. The zero degree gantry angle MLC position was checked for both the machines using EPIDs and radiographic films. Clinac iX and Clinac 2300 CD had a little effect with a mean difference in various leaf positions ranging from about −0.075 to 0.06 mm. The darkening of radiographic film always results in bigger uncertainties on these measurements. Figure 4 shows typical example for Clinac 2300 CD leaf position accuracy study on EPID and radiographic film, where alternate MLC leafs are closed from both sides.

This study shows that the advantages of actual gantry pretreatment quality assurance are totally machine dependent. There is no significant difference obtained once the mechanical quality controls are performed for gantry sagging and MLC leaf positions besides other dosimetric checks. A definite number of gantry angle IMRT plans make these studies possible, while the gantry dependent quality assurance in more complex treatments and ARC therapies is practically time consuming and difficult in fluence mapping.

4. Conclusion

Patient specific pretreatment QAs should be better done at the treatment angles, if an on-board EPID is available. Pretreatment plan verifications using EPID are preferred to be in gantry angle dependent positions but it was also shown that such requirement is not strictly necessary. If the periodic quality assurances are performed, then the pretreatment IMRT QA could be executed at zero degree gantry angles as well, with considerable time reduction to perform the quality control for each patient. In fewer cases, the zero degree pretreatment analysis is even better than actual degree gantry angles. In a treatment facility where on-board EPID is not available, the time consuming gantry dependent QA using 2D arrays can be restricted to zero gantry angle pretreatment verifications. However, zero degree gantry angle pretreatment plan verifications cannot be employed in continuous arc treatments (i.e., gantry speed stability affects the dose delivery), where gantry dependent quality assurance is difficult.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The authors sincerely acknowledge the assistance provided by Mr. K. K. Shakir and Mr. A. Siddartha (Medical Physicists, AJ Cancer Institute, Mangalore, India) during the experiments. They are grateful to Professor Dr. Jayaram Shetty (Oncologist, K. S. Hegde Medical Academy, Mangalore, India) for his periodic suggestions.

References

  1. D. A. Low, S. Mutic, J. F. Dempsey et al., “Quantitative dosimetric verification of an IMRT planning and delivery system,” Radiotherapy and Oncology, vol. 49, no. 3, pp. 305–316, 1998. View at: Publisher Site | Google Scholar
  2. S. C. Vieira, M. L. P. Dirkx, B. J. M. Heijmen, and H. C. J. de Boer, “SIFT: a method to verify the IMRT fluence delivered during patient treatment using an electronic portal imaging device,” International Journal of Radiation Oncology Biology Physics, vol. 60, no. 3, pp. 981–993, 2004. View at: Publisher Site | Google Scholar
  3. M. van Zijtveld, M. Dirkx, M. Breuers, H. de Boer, and B. Heijmen, “Portal dose image prediction for in vivo treatment verification completely based on EPID measurements,” Medical Physics, vol. 36, no. 3, pp. 946–952, 2009. View at: Publisher Site | Google Scholar
  4. A. S. Ali, M. L. P. Dirkx, R. M. Cools, and B. J. M. Heijmen, “Accurate IMRT fluence verification for prostate cancer patients using “in-vivo” measured EPID images and in room acquired kilovoltage cone-beam CT scans,” Radiation Oncology, vol. 8, pp. 211–218, 2013. View at: Publisher Site | Google Scholar
  5. P. E. Engström, P. Haraldsson, T. Landberg, H. S. Hansen, S. A. Engelholm, and H. Nyström, “In vivo dose verification of IMRT treated head and neck cancer patients,” Acta Oncologica, vol. 44, no. 6, pp. 572–578, 2005. View at: Publisher Site | Google Scholar
  6. P. B. Greer and C. C. Popescu, “Dosimetric properties of an amorphous silicon electronic portal imaging device for verification of dynamic intensity modulated radiation therapy,” Medical Physics, vol. 30, no. 7, pp. 1618–1627, 2003. View at: Publisher Site | Google Scholar
  7. M. van Zijtveld, M. L. P. Dirkx, H. C. J. de Boer, and B. J. M. Heijmen, “Dosimetric pre-treatment verification of IMRT using an EPID; clinical experience,” Radiotherapy and Oncology, vol. 81, no. 2, pp. 168–175, 2006. View at: Publisher Site | Google Scholar
  8. L. N. McDermott, M. Wendling, B. van Asselen et al., “Clinical experience with EPID dosimetry for prostate IMRT pre-treatment dose verification,” Medical Physics, vol. 33, no. 10, pp. 3921–3930, 2006. View at: Publisher Site | Google Scholar
  9. P. W. Chin, D. G. Lewis, and E. Spezi, “Correction for dose-response variations in a scanning liquid ion chamber EPID as a function of linac gantry angle,” Physics in Medicine and Biology, vol. 49, no. 8, pp. N93–N103, 2004. View at: Publisher Site | Google Scholar
  10. G. Yan, C. Liu, T. A. Simon, L.-C. Peng, C. Fox, and J. G. Li, “On the sensitivity of patient-specific IMRT QA to MLC positioning errors,” Journal of Applied Clinical Medical Physics, vol. 10, no. 1, pp. 120–128, 2009. View at: Google Scholar
  11. M. Mohammadi, E. Bezak, and P. Reich, “Verification of dose delivery for a prostate sIMRT treatment using a SLIC-EPID,” Applied Radiation and Isotopes, vol. 66, no. 12, pp. 1930–1938, 2008. View at: Publisher Site | Google Scholar
  12. M. F. Clarke and G. J. Budgell, “Use of an amorphous silicon EPID for measuring MLC calibration at varying gantry angle,” Physics in Medicine and Biology, vol. 53, no. 2, pp. 473–485, 2008. View at: Publisher Site | Google Scholar
  13. A. van Esch, T. Depuydt, and D. P. Huyskens, “The use of an aSi-based EPID for routine absolute dosimetric pre-treatment verification of dynamic IMRT fields,” Radiotherapy and Oncology, vol. 71, no. 2, pp. 223–234, 2004. View at: Publisher Site | Google Scholar
  14. W. Ulmer, J. Pyyry, and W. Kaissl, “A 3D photon superposition/convolution algorithm and its foundation on results of Monte Carlo calculations,” Physics in Medicine and Biology, vol. 50, no. 8, pp. 1767–1790, 2005. View at: Publisher Site | Google Scholar
  15. International Atomic Energy Agency (IAEA), “Absorbed dose determination in external beam radiotherapy: an international code of practice for dosimetry based standards of absorbed dose to water,” Technical Reports Series 398, Vienna, Austria, 2000. View at: Google Scholar
  16. AERB Safety Guide, “Codes, standards and guides to be prepared by the regulatory body for nuclear and radiation facilities, AERB/RSD/RT/COM,” Atomic Energy Regulatory Board, Mumbai, India, 2001. View at: Google Scholar
  17. Portal Imaging and Portal Dosimetry Reference Guide, Varian Medical Systems, Palo Alto, Calif, USA, 2008.
  18. T. Depuydt, A. van Esch, and D. P. Huyskens, “A quantitative evaluation of IMRT dose distributions: refinement and clinical assessment of the gamma evaluation,” Radiotherapy and Oncology, vol. 62, no. 3, pp. 309–319, 2002. View at: Publisher Site | Google Scholar
  19. R. Brun and F. Rademakers, “ROOT—an object oriented data analysis framework,” Nuclear Instruments and Methods in Physics Research A, vol. 389, no. 1-2, pp. 81–86, 1997, Proceedings of the AIHENP '96 Workshop, Lausanne, Switzerland, September 1996. View at: Publisher Site | Google Scholar

Copyright © 2014 Siji Cyriac et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


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