- Open Access
Statistical analysis of IMRT dosimetry quality assurance measurements for local delivery guideline
© Chung et al; licensee BioMed Central Ltd. 2011
Received: 26 October 2010
Accepted: 28 March 2011
Published: 28 March 2011
To establish our institutional guideline for IMRT delivery, we statistically evaluated the results of dosimetry quality assurance (DQA) measurements and derived local confidence limits using the concept confidence limit of |mean|+1.96σ.
Materials and methods
From June 2006 to March 2009, 206 patients with head and neck cancer, prostate cancer, liver cancer, or brain tumor were treated using LINAC-based IMRT technique. In order to determine site specific DQA tolerances at a later stage, a hybrid plan with the same fluence maps as in the treatment plan was generated on CT images of a cylindrical phantom of acryl. Points of measurement using a 0.125 cm3 ion-chamber were typically located in the region of high and uniform doses. The planar dose distributions perpendicular to the central axis were measured by using a diode array in solid water with all fields delivered, and assessed using gamma criteria of 3%/3 mm. The mean values and standard deviations were used to develop the local confidence and tolerance limits. The dose differences and gamma pass rates for the different treatment sites were also evaluated in terms of total monitor uints (MU), MU/cGy, and the number of PTV's pieces.
The mean values and standard deviations of ion-chamber dosimetry differences between calculated and measured doses were -1.6 ± 1.2% for H&N cancer, -0.4 ± 1.2% for prostate and abdominal cancer, and -0.6 ± 1.5% for brain tumor. Most of measured doses (92.2%) agreed with the calculated doses within a tolerance limit of ±3% recommended in the literature. However, we found some systematic under-dosage for all treatment sites. The percentage of points passing the gamma criteria, averaged over all treatment sites was 97.3 ± 3.7%. The gamma pass rate and the agreement of ion-chamber dosimetry generally decreased with increasing the number of PTV's pieces, the degree of modulation (MU/cGy), and the total MU beyond 700. Our local confidence limits were comparable to those of AAPM TG 119 and ESTRO guidelines that were provided as a practical baseline for center-to-center commissioning comparison. Thus, our institutional confidence and action limits for IMRT delivery were set into the same levels of those guidelines.
Discussion and Conclusions
The systematic under-dosage were corrected by tuning up the MLC-related factors (dosimetric gap and transmission) in treatment planning system (TPS) and further by incorporating the tongue-and groove effect into TPS. Institutions that have performed IMRT DQA measurements over a certain period of time need to analyze their accrued DQA data. We confirmed the overall integrity of our IMRT system and established the IMRT delivery guideline during this procedure. Dosimetric corrections for the treatment plans outside of the action level can be suggested only with such rigorous DQA and statistical analysis.
Beamlet-based intensity modulated radiation therapy (IMRT) represents a significant advance in conformal radiation therapy in terms of target dose conformity and normal tissue saving. The dosimetric advantage of IMRT over conventional techniques has been well documented in the literature [1–7]. Due to the inherent complexity in planning and delivery, a comprehensive quality assurance (QA) that ensures the whole process of IMRT should be carried out prior to the treatment [8–11]. Many of the justification, philosophy, and requirements for the IMRT QA program were given in the AAPM and ESTRO guidance document and others [10, 12, 13]. Patient-specific IMRT quality assurance is one of essential tasks to ensure accurate dose delivery to the patient [14–17]. It often consists of measuring point doses and 2D dose distributions in a phantom. Ion-chambers and 2D arrays of ion-chambers or diodes have been used for this purpose.
Dong et al.  extensively analyzed IMRT QA results and found that accuracy in QA of up to ±7% and spatial accuracy of ±5 mm could be achieved. Pawlicki and co-workers [19, 20] have reported on the use of control charts for radiotherapy quality assurance of linear accelerators using both hypothetical and clinical data. Breen et al.  proposed statistical process control (SPC) concepts for IMRT dosimetric verification. The purpose of SPC was to monitor performance continuously, by testing that the mean and dispersion of the measured data was stable over time. Recently the AAPM TG 119 suggested that the confidence limit for ion-chamber measurements in the target region was 4.5% . For 2D dose comparison, 94% passing rate in gamma criteria  of ±3%/3 mm for individual fields and 75% in gamma criteria of ±4%/3 mm for combined fields were proposed in multi-center head and neck IMRT trials . The confidence limit does provide a mechanism for determining reasonable action levels for per-patient IMRT verification studies . The consistency and confidence in advance technology multi-institutional clinical trials was emphasized in the literature [24, 25].
We have performed patient-specific IMRT DQA measurements for 206 patients with head and neck (H&N) cancer, brain tumor, abdominal or prostate cancer. Most of point dose measurements (92.2%) agreed with calculated values within ±3%. The average gamma pass rate for criteria of ±3%/3 mm was 97.3 ± 3.7%. However, as reported by international recommendations, treatment planning and delivery in radiation therapy will be never perfect. Thus, we are always engaged to answer the practical question of "how good is good enough or especially what is a reasonable and achievable standard for IMRT commissioning and delivery?" As an institution that has implemented IMRT we statistically analyzed the IMRT DQA results to address this question. Our local values resulted from this study were compared with the tables of AAPM TG 119 report that were provided as a practical baseline for center-to-center comparison. In addition we investigated the agreement of point dose measurements and gamma pass rate for different tumor sites, the number of PTV's pieces, degree of modulation, and the total MU. Based on this rigorous approach, we established our institutional guideline for IMRT delivery.
Materials and methods
Planning and Optimization Procedure
From June 2006 to March 2009, 206 patients were treated with IMRT using a Varian Clinac™ 6EX or 21EX Linac equipped with a 120 Millennium™ MLC (Varian Medical Systems, Palo Alto, CA). Patients were grouped into 89 (43.2%) patients with H&N cancer, 42 (20.3%) patients with brain tumor, and 75 (36.4%) patients with abdominal or prostate cancer. IMRT treatment plans consisted of 5 - 11 fields with 6 or 15 MV x-ray beam. Treatment plans were optimized with the Eclipse™ RTP system (version 7.0, Varian, Palo Alto, USA). The optimization process, based on physical constraints in terms of an objective function that describes the limits of acceptance and the goals desired for the dose distribution, created optimized fluence distributions for a number of pre-selected beams, and then transformed them into dynamic MLC movements . The calculation grid used for the final dose distributions was 2.5 mm × 2.5 mm. Especially in H&N cases, the simultaneous integrated boost (SIB) technique was used for concave dose distributions that included the primary tumor and lymph nodes on both sides of the neck . A dose of 2.25 Gy per fraction was delivered to the primary tumor site and involved lymph nodes, and 1.8 Gy per fraction to elective lymph node groups.
We paid special attention to any individual field with dose differences larger than 10%. In such cases, another verification plans on CT images of solid water slabs (30 × 30 × 20 cm3) were generated to compare calculated and measured 2D dose distributions. All parameters of the treatment plans were identically applied, except for changing the gantry angle to 0 degree. The dose distribution at 5 cm depth from the slab surface was calculated in the TPS and exported for comparison with the measured distribution. Measurements were performed by using a 2D diode array (MapCheck, Sun Nuclear, USA) located at the same 5 cm depth. The evaluation of discrepancy between measured and calculated dose distributions was carried out by using γ-index method [17, 22–24] with criteria of 3 mm DTA (distance to agreement) and 3% dose difference. The gamma analysis was restricted to regions to avoid those of very low dose. This was done by defining the region of interest using a threshold dose that was set to 10% of the maximum dose.
Statistical analysis of high dose point in the PTV measured with ion-chamber: [(measured dose)-(calculated dose)]/calculated dose, with associated confidence limit
Standard deviation (σ)
I/C1 or near I/C
I/C or near I/C
Head and Neck
I/C or near I/C
Confidence limit = (|mean|+1.96σ)
Percentage of points passing gamma criteria of 3%/3 mm, with associated confidence limits
Standard deviation (σ)
Head and Neck
Confidence Limit = (100-mean)+1.96σ
10.0% (i.e., 90% passing)
The sources of discrepancy between calculated and measured doses are positioning errors of dynamic MLC, insufficient dosimetric data of dynamic MLC in TPS, inaccurate handling of small field dosimetry, and some user's errors and inaccurate measurement devices for setting IMRT QA procedures [29–33]. The accuracy of IMRT DQA results was significantly attributed to dosimetric data of dynamic MLC in TPS such as dosimetric gap, interleaf and mid-leaf leakage, whether tongue-and-groove effect was appropriately handling or not in TPS. The dosimetric gap and leakage of MLC inserted into our TPS were 1.8 mm for 6 MV and 1.875 mm for 15 MV, and 1.6% for 6 MV and 1.8% for 15 MV, respectively, which were consistent with the data used in the other institutions with the same machine and TPS.
The other source of errors in TPS can be the tongue-and-groove effect that often results in under-dosage [34, 35]. The tongue-and-groove effect wasn't incorporated into the TPS used in this study. This could more or less contribute to the systematic under-dosage revealed in this study. Recent upgrade of our IMRT system included (1) an advanced dose calculation algorithm that accounts for the tongue-and-groove effect (Eclipse™ 8.6) and (2) the MLC control software (7.2.1 version) that can improve MLC-positioning accuracy. Owing to such improvement, recent results of our DQA measurements don't reveal any noticeable systematic bias. Highly-modulated plans seemed to be more sensitive to accuracies of the above sources of errors than mildly-modulated plans. About 7.8% of highly-modulated H&N plans didn't satisfy ±3% criteria, while the abdominal or prostate IMRT DQA results showed a better agreement (97.3%) than the H&N cases. However, systematic under-dosage was shown in all treatment sites examined in this study. Even considering a large daily dose (225 cGy) of H&N plans compared to a daily dose (200 cGy) of prostate and brain plans, total MU of H&N was much higher that other sites shown in figure 1. This implies the under-dosage trend as increasing the degree of modulation. The complexity of highly-modulated plans most likely exacerbated such a trend of under-dosage. In addition, per-field measurements (see figure 3) showed a broader deviation in H&N than in prostate. This was related to high dose gradients near a point of measurement in highly-modulated H&N plans. With such high dose gradients, a setup error of even less than 1 mm can attribute to a large deviation of per-field measurements.
Recently, IMRT has evolved toward the use of many small radiation fields. Therefore, small ion-chambers with sensitive volumes of ~0.1 cc were often employed for IMRT verification [36, 37]. We used an ion-chamber with a 0.125 cc sensitive volume that was the same type of detectors used in most of institutions involved in the AAPM TG 119 study. We believed that the absolute dose error for the IMRT verification measurement within a uniform and high dose region of PTV was minuscule .
Our local confidence limits for both measurements using the ion-chamber and 2D array of diodes were on the same order or less than AAPM TG 119 data  and/or ESTRO guidelines . 7.8% of our ion-chamber DQA data were out of ±3% criteria but none of them were on the action level of ±5% recommended in reference 12 and 13. The systematic under-dosage could be corrected by tuning up the MLC-related factors (dosimetric gap, tongue-and-groove effect, and transmission) in the TPS. Institutions that have implemented IMRT in the clinic and performed DQA measurements over a certain period of time need to analyze their DQA data. We confirmed the overall integrity of our IMRT system and established the IMRT delivery guideline during this procedure. Dosimetric corrections for the treatment plans outside of the action levels can be suggested only with such rigorous DQA and statistical analysis.
This work was in part supported by the National Research Foundation of Korea (NRF) grant (2010-0029589) funded by the Korea government (MEST).
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