Equivalence of Gyn GEC-ESTRO guidelines for image guided cervical brachytherapy with EUD-based dose prescription
- William Shaw^{1}Email author,
- William ID Rae^{1} and
- Markus L Alber^{2}
https://doi.org/10.1186/1748-717X-8-266
© Shaw et al.; licensee BioMed Central Ltd. 2013
Received: 27 September 2013
Accepted: 8 November 2013
Published: 13 November 2013
Abstract
Background
To establish a generalized equivalent uniform dose (gEUD) -based prescription method for Image Guided Brachytherapy (IGBT) that reproduces the Gyn GEC-ESTRO WG (GGE) prescription for cervix carcinoma patients on CT images with limited soft tissue resolution.
Methods
The equivalence of two IGBT planning approaches was investigated in 20 patients who received external beam radiotherapy (EBT) and 5 concomitant high dose rate IGBT treatments. The GGE planning strategy based on dose to the most exposed 2 cm^{3} (D2cc) was used to derive criteria for the gEUD-based planning of the bladder and rectum. The safety of gEUD constraints in terms of GGE criteria was tested by maximizing dose to the gEUD constraints for individual fractions.
Results
The gEUD constraints of 3.55 Gy for the rectum and 5.19 Gy for the bladder were derived. Rectum and bladder gEUD-maximized plans resulted in D2cc averages very similar to the initial GGE criteria. Average D2ccs and EUDs from the full treatment course were comparable for the two techniques within both sets of normal tissue constraints. The same was found for the tumor doses.
Conclusions
The derived gEUD criteria for normal organs result in GGE-equivalent IGBT treatment plans. The gEUD-based planning considers the entire dose distribution of organs in contrast to a single dose-volume-histogram point.
Keywords
Background
Recently, the treatment of cervical cancer has been advanced through the use of image guided brachytherapy (IGBT) [1–4]. The Groupe Européen de Curiethérapie (GEC) and the European SocieTy for Radiotherapy & Oncology (ESTRO) working group (Gyn GEC-ESTRO WG, GGE) presented guidelines that comprise imaging and organ segmentation for planning of every treatment fraction [5, 6]; subsequently, limited imaging approaches have been derived [7, 8]. Such an approach adapts for organ motion and tumor shape changes by conforming the prescribed dose to the target volume of the day, and thereby increases the chance of applying effective IGBT doses in successive fractions. This image- and volume-based planning strategy allows for a per-fraction analysis of dose distributions and dose volume histograms (DVHs). Further, the total delivered dose up to and including the last treatment fraction can be estimated for clinical target volumes (CTV) and organs at risk (OAR). This constitutes a risk-controlled dose prescription method with DVH criteria for tumor and normal tissue volumes. The relevance of these criteria has been demonstrated by linking them to toxicity [9–11] and local control [11–14]. However, contouring and organ motion are the major contributors of uncertainties in IGBT [15].
The GGE technique requires MRI for tumor and OAR delineation with applicators in-situ. Unfortunately many clinics have limited availability of MRI. One alternative is CT imaging, but due to the lower contrast, CT based planning results in increased OAR volumes, CTV delineation uncertainty and consequently unnecessarily large CTVs, as one tends to plan conservatively [16–19]. These uncertainties can produce lower CTV doses [3, 16] if normal tissue DVH criteria are adhered to. At the same time, contour uncertainty leads to uncertainty of derived DVH criteria for toxicity scoring or tumor control and an uncertainty in the addition of OAR and tumor DVHs for obtaining worst-case estimates of the accumulated dose [6, 15, 20, 21]. Furthermore, with the increased use of more conformal external beam radiotherapy (EBT) techniques such as intensity modulated radiotherapy (IMRT), the addition of DVH parameters for such worst case estimates can become unreliable.
This raises the question whether a volume-based treatment plan metric such as the equivalent uniform dose (EUD) [22] could be more robust against contouring and imaging uncertainties than DVH. In EBT planning, the generalized EUD (gEUD) is well established [23–25] and is mathematically equivalent to the DVH reduction scheme of the Lyman-Kutcher-Burman (LKB) normal tissue complication probability (NTCP) model [26–29]. It is our intention to establish a gEUD-based prescription method for IGBT that can replace the original GGE prescription in terms of dose-volume criteria, but offers advantages in terms of safety and robustness against uncertainties. Further, EUD sports favorable mathematical properties that allow a reliable worst-case estimate of the accumulated dose.
We investigate this question with a three-stage planning study of fractionated IGBT. In stage 1, we record the EUD values of OARs achieved with plans obtained from the dose-volume constrained GGE guidelines. From this, we establish corresponding EUD criteria. In stage 2, the treatments are planned according to these EUD constraints, and their safety is assessed according to the GGE DVH criteria. Finally, in stage 3, the full treatments (EBT + 5 fractions IGBT) of both strategies are compared by both metrics.
Methods
Patient selection, imaging and contouring
Patient, volume and treatment characteristics
Characteristic | No of patients and/or value(s) |
---|---|
Total nr of patients | 20 |
Total EBT dose | 50 Gy |
Total nr of EBT fractions | 25 |
Total nr of IGBT fractions | 5 |
Total IGBT dose (Mean ± SD) | 4.7 ± 0.8 Gy |
Total nr of CT datasets in study | 100 |
FIGO stage (n) | |
II | 5 |
III | 12 |
IVa | 3 |
Volume in cc (Mean ± SD) | |
HR-CTV @ 1 ^{ st } IGBT treatment | 49.0 ± 21.0 |
IR-CTV @ 1 ^{ st } IGBT treatment | 119.0 ± 43.0 |
Rectum | 94.8 ± 32.6 |
Bladder | 108.0 ± 91.6 |
Dose objectives/constraints | |
HR-CTV D90 | ≥ 85 Gy |
IR-CTV D90 | ≥ 60 Gy |
Rectum D2cc | ≤ 70 Gy |
Bladder D2cc | ≤ 80 Gy |
Contouring was based on clinical examination and CT images, using the GGE guidelines for the HR-CTV, Intermediate Risk CTV (IR-CTV) and the rectum and bladder walls. The GTV had to be omitted as it cannot be identified on CT images. The HR-CTV consisted of the whole cervix and macroscopic extent of the disease at the time of imaging for IGBT. The IR-CTV encompassed the HR-CTV plus a variable margin depending on the initial extent of the disease, considering tumor regression in response to treatment. The OAR walls and outline with content were delineated according to the same set of recommendations.
Fractionation and dose evaluation parameters
According to the GGE recommendations we recorded the following parameters for purposes of comparison: Minimal dose received in 0.1, 1, and 2 cc of the maximal dose regions of the OARs (D0.1, 1, 2 cc; outer wall plus content), dose to 90% (D_{90}) of the HR- and IR-CTVs, as well as the EUDs of OAR walls and CTVs.
Full DVHs of each treatment fraction were available in the Flexiplan (Nucletron®) treatment planning system and dose was converted to a 2 Gy equivalent dose (EQD2) [30]. According to GGE, the linear quadratic (LQ) model parameters of α/β being 3 Gy for OARs and 10 Gy for tumors (α being 0.3 Gy^{-1}) were applied. Since the treatment was concomitant HDR brachytherapy, repair half-times and repopulation were neglected.
S is calculated from D_{ k }, the dose bin for the v_{k-th} fractional tumor volume.
where D_{k} is the EQD2 for the v_{k-th} fractional OAR volume and a is the volume effect parameter. The gEUD for rectum and bladder walls was calculated using volume effect parameters (a) of 12 for the rectum and 8 for the bladder [23, 32, 33].
For simplicity we refer to the EUD based, adaptive IGBT planning strategy as the comprehensive volume technique (CV), emphasizing the fact that EUD considers the entire organ volume.
Study 1: prescription constraints
One possibility to establish the gEUD prescription constraints for IGBT treatment planning is to collect them from literature, another by a planning study. From Söhn et al. (2007), we can choose the gEUD upper limit for the rectum to be 67.8 Gy (3.55 Gy EUD per IGBT fraction), at approximately 10% NTCP for grade II (G2) rectal bleeding. However, in the following this gEUD is verified against a rectum D2cc constraint of 70 Gy EQD2 [9, 10] by the planning study. Bladder NTCP model data are scarce and uncertain [34] due to unaccounted variations in filling. Consequently, the bladder gEUD constraint is determined by the planning study. There are bladder dose guidelines based on the GGE work that show more than 5 - 10% late complication rates when the D2cc is in the order of 70–100 Gy EQD2 [9, 10, 19, 35, 36].
To derive the bladder wall gEUD dose constraints, the GGE planning strategy was followed to achieve at least 7.0 Gy per fraction (85 Gy EQD2 from EBT and IGBT) to the HR-CTV D90. Treatment plans were produced for each treatment fraction on the 100 CT datasets. Each plan started from the standard loading pattern and was manually or graphically optimized until the HR-CTV dose objective was reached, or until one of the two OAR constraints in question prevented any further CTV dose escalation (Table 1). Bladder EUD constraints: HR-CTV dose was further increased beyond the CTV objective until the bladder D2cc criterion was reached. This constraint was chosen as 80 Gy total dose from EBT and IGBT, resulting in 6 Gy EQD2 per IGBT fraction. The procedure was repeated on all plans and for each the associated bladder wall gEUD was computed. Consequently, the bladder wall gEUD is solely determined by the D2cc of the bladder and is not influenced by any other OAR criterion or the CTV doses. Rectum EUD constraints: To verify the chosen gEUD of 67.8 Gy for an upper rectal limit, we repeated this constraint derivation procedure for the rectal wall by limiting the total rectum D2cc EQD2 to 70 Gy (4.0 Gy EQD2 per fraction).
All 100 “bladder-limited” plans are maximized to the bladder constraint of 6.0 Gy D2cc per fraction and the corresponding bladder wall gEUDs were recorded and all 100 “rectum-limited” plans are maximized to the rectum dose constraint of 4.0 Gy D2cc and the associated rectum wall gEUDs were recorded. From these data, the variation in bladder and rectal wall gEUD at fixed DVH criteria could be found and the EUD criteria could be derived or verified from these gEUD frequency distributions.
Study 2: safety of EUD constraints in terms of GGE constraints
To test the safety of the CV technique, we investigated the appropriateness of the bladder- and rectum wall EUD constraints in terms of the GGE dose volume criteria. Here we maximized the same dose distribution as in study 1 for each treatment plan, but to the point where the bladder wall gEUD constraint was reached instead of the D2cc constraint. At this point we recorded the corresponding D2cc (and other DVH parameters). This procedure was repeated for the rectal wall by maximizing dose to the rectum gEUD constraint. Thus a single plan was optimized against each of the organs at risk separately.
Study 3: comparison of GGE and CV planning strategies for the entire treatment
Once the robustness of the CV technique in each fraction has been established, the two planning strategies can be compared in terms of OAR and CTV dose for a full treatment. The GGE based plans for each patient and each fraction adhered to the two OAR D2cc constraints (Table 1) per fraction, whichever was met first. The HR-CTV D90 was targeted to be at least 85 Gy in total. No upper CTV constraints were set and dose was maximized until an OAR D2cc constraint was reached. The total dose from IGBT and EBT was calculated. For the CV technique the OAR EUD constraints were employed that were found earlier. Finally, the two strategies could be compared in terms of D90, D2cc and EUD.
Results
Prescription constraints
Summary of the statistical parameters of the gEUD variations with D2cc and EUD criteria
Statistical measure | Dose (Gy) GGE strategy | Dose (Gy) CV strategy |
---|---|---|
Bladder D2cc/gEUD constraint (planning) | 6.00 | 5.19 |
Bladder Wall gEUD/D2cc | ||
Mean | 5.19/6.00 | 5.19/6.25 |
SD | 1.25/0.00 | 0.00/1.01 |
Bladder D0.1 cc | ||
Mean | 9.97 | |
SD | 0.85 | |
Bladder D1cc | ||
Mean | 7.21 | |
SD | 0.98 | |
Rectum D2cc/gEUD constraint (planning) | 4.00 | 3.55 |
Rectum Wall gEUD/D2cc | ||
Mean | 3.67/4.00 | 3.55/3.96 |
SD | 0.53/0.00 | 0.00/0.49 |
Rectum D0.1 cc | ||
Mean | 5.80 | |
SD | 0.29 | |
Rectum D1cc | ||
Mean | 4.46 | |
SD | 0.44 |
The average gEUD of the rectal wall at a D2cc constraint of 4.0 Gy was 3.67 Gy (±0.53 Gy) which is comparable to the 3.55 Gy from our external beam rectum EUD constraint choice. If this average gEUD was reached in all of the 5 fractions, the NTCP would be ranking at approximately 11%. The average bladder gEUD at a D2cc constraint of 6.0 Gy was 5.19 Gy (±1.25 Gy). The values: rectum wall gEUD ≤ 3.55 Gy and bladder wall gEUD ≤ 5.19 Gy were established as the upper limits for the CV technique. Thus, the total EUD constraint for the bladder wall equals 75.95 Gy.
Safety of EUD criteria in terms of GGE criteria
Different gEUD(x) levels resulting in percentage x of treatment fractions with D2cc larger than the GGE constraint and mean and standard deviations of the resulting distributions
x % of treatment fractions | Rectum gEUD(x) (Gy) | Rectum mean D2cc ± SD (Gy) | Bladder gEUD(x) (Gy) | Bladder mean D2cc ± SD (Gy) |
---|---|---|---|---|
10 | 3.12 | 3.49 ± 0.43 | 4.22 | 5.11 ± 0.81 |
25 | 3.35 | 3.74 ± 0.46 | 4.48 | 5.42 ± 0.86 |
48 | 3.55 | 3.96 ± 0.49 | ||
50 | 3.58 | 3.99 ± 0.50 | 4.86 | 5.87 ± 0.94 |
70 | 5.19 | 6.25 ± 1.01 |
We have also found very good correlations between D0.1 cc and D2cc for the rectum (R^{2} = 0.84), as well as excellent correlation between D1cc and D2cc for the rectum (R^{2} = 0.96). This means that if D2cc can be controlled via the use of the EUD, ulcerations, fistulas and rectal bleeding will also be controlled. Similarly, we have found excellent correlation between bladder D1cc and D5cc with D2cc (R^{2} = 0.95 and R^{2} = 0.93 respectively), and a worse correlation between D0.1 cc and D2cc (R^{2} = 0.63).
Comparison of GGE and CV planning strategies
Summary of the statistical variations of the DVH parameters and EUD variations over the full treatment course
Statistical measure | Technique | Rectum | Bladder | HR-CTV | IR-CTV |
---|---|---|---|---|---|
D2cc | D2cc | D90 | D90 | ||
Mean (Gy) | GGE | 64.85 | 78.29 | 108.49 | 75.85 |
SD | 3.10 | 2.29 | 20.59 | 5.22 | |
Mean (Gy) | CV | 64.51 | 77.87 | 107.77 | 75.36 |
SD | 3.20 | 3.70 | 21.95 | 6.16 | |
gEUD | gEUD | EUD | EUD | ||
Mean (Gy) | GGE | 63.66 | 74.53 | 114.28 | 81.51 |
SD | 3.42 | 4.58 | 16.40 | 4.12 | |
Mean (Gy) | CV | 63.18 | 73.32 | 113.58 | 81.19 |
SD | 3.07 | 3.31 | 17.90 | 5.07 |
Discussion
We have established OAR gEUD criteria for IGBT treatments that are very comparable to those obtained from the GEC-ESTRO guidelines. EUD constraints can thus be considered a safe and efficient alternative to D2cc criteria.
Compared to a D2cc constraint, which considers an isolated small volume, gEUD has the advantage to consider the dose distribution in the OAR comprehensively and still give high doses a large weight, especially if the volume effect parameter a is significantly greater than 1. For the same reason, it is also less sensitive to contouring and may therefore be a more robust choice if MRI is not available for IGBT planning. To see this, assume that contouring errors lead to errors in the volume of the dose bins of the DVH. Applying the laws of error propagation, we find that the error in D2cc is proportional to the inverse slope of the DVH at D2cc (which tends to be shallow in BT) and proportional to the volume error at that dose bin. In contrast, the error in gEUD is both proportional to the weighted root-mean-square of the volume errors in the dose bins (thus less dependent on a single bin) and smaller by a factor 1/a. This ties in with the intuition, that any kind of average over a number of uncertain quantities (such as EUD) is less uncertain than any single one of these quantities.
The derived EUD criteria depend on the reference D2cc criteria and the volume effect parameter a. Since gEUD is a power-law function of dose, it scales with the same factor as D2cc. Small deviations from this law are caused by the EQD2 correction. Within reason, our criteria can therefore be calibrated to different fractionation schemes, i.e. scaled by the ratio of the desired D2cc versus the value used here.
Variation of gEUD and D2cc for different values of the gEUD volume parameter
Volume parameter (a) | Rectum gEUD constraint (Gy)* | Rectum D2cc (Gy) ^{ # } | Bladder gEUD constraint (Gy)** | Bladder D2cc (Gy) ^{ ## } |
---|---|---|---|---|
8 | 3.09 ± 0.37 | 4.66 ± 0.52 | 5.19 ± 1.25 | 6.25 ± 1.01 |
9 | 3.26 ± 0.42 | 4.43 ± 0.51 | 5.56 ± 1.44 | 5.89 ± 1.00 |
10 | 3.41 ± 0.46 | 4.24 ± 0.50 | 5.89 ± 1.61 | 5.60 ± 0.99 |
11 | 3.54 ± 0.50 | 4.09 ± 0.50 | 6.19 ± 1.77 | 5.35 ± 0.97 |
12 | 3.67 ± 0.53 | 3.96 ± 0.49 | 6.46 ± 1.91 | 5.15 ± 0.96 |
13 | 3.78 ± 0.56 | 3.85 ± 0.49 | 6.72 ± 2.04 | 4.98 ± 0.95 |
14 | 3.88 ± 0.59 | 3.75 ± 0.48 | 6.95 ± 2.16 | 4.83 ± 0.93 |
15 | 3.97 ± 0.61 | 3.67 ± 0.48 | 7.17 ± 2.26 | 4.70 ± 0.92 |
16 | 4.06 ± 0.63 | 3.60 ± 0.47 | 7.36 ± 2.36 | 4.59 ± 0.91 |
Occasionally, the use of EUD criteria for IGBT is safer than D2cc. Observe the outliers in Figure 1 which are caused by rare unfavorable organ geometries that bring a lot of the organ volume close to the high dose region. In contrast, EUD criteria do not produce excessive D2cc values because of their mathematical construction, which gives very high weights to sub-volumes with a high dose. From Table 2, the average D2cc for the OARs, when dose is maximized to each OAR’s gEUD constraint, is virtually the same as the GGE-D2cc that was used to derive the EUD criteria. Although there is some dispersion of D2ccs around this average, none of the D2ccs were found to be unacceptably high. If the EUD constraints are reduced, as shown in Table 3, to decrease D2cc constraint violations, small changes in EUD result in large reductions in D2cc and a smaller variance of D2cc. Our results suggests that a 6 to 8% reduction in OAR gEUDs produce more than 25% fewer treatment plans that could violate a D2cc constraint. Since we know that D0.1 cc and D1cc also correlates well with D2cc, CV plans that control D2cc would subsequently control the resultant D0.1 cc and D1cc DVH parameters as well.
Summary of the average DVH parameters in total dose (Gy) of the CV treatment technique, compared to other published values
DVH parameter | CV | Georg et al.[9] | Georg et al.[10] | Levitchi et al.[33] | Jürgenliemk-Schulz et al.[38] | Jürgenliemk-Schulz et al.[39] | Nesvacil et al.[40] | Lindegaard et al.[41] |
---|---|---|---|---|---|---|---|---|
Method | HDR | HDR | HDR | PDR | PDR | HDR/PDR | HDR | PDR |
Rectum | ||||||||
D0.1 cc | 79 ± 1 | 88 ± 10* | 83 - 132 ^{ a } | 83 ^{ b } | ||||
81 ± 13** | 86 ± 27** | 65 ± 15** | 74 ± 9** | |||||
D1cc | 72 ± 2 | 76 ± 7* | 71 - 87 ^{ a } | |||||
70 ± 9** | 69 ± 14** | 69 ± 6** | ||||||
D2cc | 70 ± 2 | 72 ± 6* | 67 - 78 ^{ a } | 68 ^{ b } | ||||
66 ± 8** | 65 ± 12** | 57 ± 8** | 66 ± 6** | 54 ± 2** ^{ c } | 57 ± 6** | 67 ± 6** | ||
69 ± 2** ^{ d } | ||||||||
Bladder | ||||||||
D0.1 cc | 100 ± 3 | 61 - 178 ^{ a } | 109 ^{ b } | |||||
162 ± 75** | 78 ± 22** | 86 ± 12** | ||||||
D1cc | 86 ± 3 | 71 - 116 ^{ a } | ||||||
108 ± 31** | 77 ± 8** | |||||||
D2cc | 81 ± 3 | 70 – 101 ^{ a } | 72 ^{ b } | 81 ± 6** | 53 ± 2** ^{ c } | 76 ± 9** | ||
95 ± 22** | 64 ± 11** | 101 ± 11** ^{ d } | 73 ± 6** |
These dose endpoints are also very comparable with studies where large HR-CTV volumes were investigated and no interstitial needles were used. As shown in the study of Jürgenliemk-Schulz et al. [36], we expect that interstitial needles would decrease the EUD of OARs in large tumor volume cases as well. For bladder, we found good correspondence with the results of Levitchi et al. [37], Jürgenliemk-Schulz et al. [36, 38], Nesvacil et al. [39] and Lindegaard et al. [40]. Since there were no upper dose boundaries for the CTV, the CTV dose is expected to spread widely, driven solely by the OAR geometries and relative positions. From Figures 3 and 4 it is clear that the CV technique does not result in under-dosage of the CTVs.
where E[] is the sum over all fractions, $\stackrel{\u0303}{D}$ is the dose of each fraction, warped to reference geometry, and D the dose as computed for the patient geometry of the particular fraction. Hence, the left hand side is the EUD of the properly accumulated total dose, while the right hand side is the sum of the EUDs as computed for each fraction individually. For target volumes, the inequality reverses. This estimate is of particular importance for pelvic radiotherapy, where deformable registration of images is difficult to perform reliably. Hence, EUD addition gives a worst case scenario for OARs and CTV without the need for deformable image registration and dose warping [42].
D2cc is not a convex function of dose and is not additive in a strict sense, so that further assumptions about the dose distribution have to be made. Jensen’s inequality also applies to maximum and minimum dose, so that, if D2cc and D90 have a strong correlation to the former, the inequality holds for the latter approximately “by proxy”. The versatility of EUD summation as worst case estimate extends to the addition of very heterogeneous OAR EBT doses, for example lymph node boosts. Finally, because there is a variability in reported dose-volume cut-offs for OARs in IGBT [9, 35, 37, 43] and these also differ from cut-offs in EBT, EUD is helpful in combining the experience in both areas and relating it to the LKB model [44]. Conversely, documented brachytherapy toxicity rates can be useful for focused dose escalation in EBT, for example dose painting.
Conclusions
Concluding, a GEC-ESTRO-like IGBT plan adaption is feasible with EUD criteria, instead of D2cc criteria. Because of the mathematical construction of gEUD, and the fact that it considers the organ volume comprehensively, it is inherently more robust against contouring uncertainties. This could make gEUD a better choice than D2cc if IGBT has to be performed on CT, instead of MR, images. The summation of EUDs per treatment fraction gives a reliable worst case estimate of the total treatment dose, which opens possibilities for safe dose escalation in IGBT or simultaneous integrated boost in EBT.
Declarations
Acknowledgements
The University of the Free State was supported by research grants from the Medical Research Foundation (MRC) of South Africa and the Aarhus University Hospital was supported by CIRRO - The Lundbeck Foundation Center for Interventional Research in Radiation Oncology and The Danish Council for Strategic Research.
Authors’ Affiliations
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