Primary tumor volume delineation in head and neck cancer: missing the tip of the iceberg?
- Olgun Elicin†1Email authorView ORCID ID profile,
- Dario Terribilini†1,
- Mohamed Shelan1,
- Werner Volken1,
- Etienne Mathier1,
- Alan Dal Pra1,
- Daniel M. Aebersold1,
- Michael K. Fix1 and
- Peter Manser1
© The Author(s). 2017
Received: 26 March 2017
Accepted: 8 June 2017
Published: 20 June 2017
The aim was to evaluate the geometric and corresponding dosimetric differences between two delineation strategies for head and neck tumors neighboring air cavities.
Primary gross and clinical tumor volumes (GTV and CTV) of 14 patients with oropharynx or larynx tumors were contoured using a soft tissue window (S). In a second strategy, the same volumes were contoured with an extension to include the parts which became visible on lung window (L). For the calculation of Hausdorff-distances (HD) between contoured volumes of the two strategies, triangular meshes were exported. Two radiotherapy plans with identical goals and optimization parameters were generated for each case. Plan_S were optimized on CTV_S, and Plan_L on CTV_L. The dose coverages of CTV_L and CTV_Δ (CTV_L minus CTV_S) were evaluated in Plan_S. OAR doses were compared among Plan_S and Plan_L.
Median three-dimensional HD for GTVs and CTVs were 5.7 (±2.6) and 9.3 (±2.8) mm, respectively. The median volume differences between structures contoured using L and S windows were 9% (±5%) and 9% (±4%) for GTV and CTV, respectively. In 13 out of 14 cases, Plan_S met the plan acceptance criteria for CTV_L. In 8 cases CTV_Δ was covered insufficiently in Plan_S. Mean and median differences in OAR dose-volume histogram parameters between Plan_S and Plan_L were within 3%.
For the current practice in radiotherapy planning for head and neck cancer, the delineation of L-based volumes seems unnecessary. However, in special settings, where smaller or no PTV margins are used, this approach may play an important role for local control.
Currently, there is a well-established international consensus among radiation oncologists for the delineation of the organs at risk (OARs) and the elective lymphatic levels for the radiotherapy planning of squamous cell head and neck cancer (SCCHN) [1, 2]. Despite the heterogeneity based on the equipment and institutional protocols, image guided treatment technologies are allowing the clinicians to reduce the margins used to generate the planning treatment volumes (PTVs) around the clinical target volumes (CTVs). It is difficult to forecast, if and when the PTV can be abolished in the future (i.e. CTV = PTV). Before reaching this goal, there is another uncertainty which needs to be addressed: the uncertainty and heterogeneity in the delineation strategy of the high-risk CTV around the primary tumor .
There are different strategies to define this high-risk CTV, most of them based on tradition, data inferred from pathology results and patterns of failure. One method is based on pre-defined anatomical subsites , whereas the other approach uses an isotropic expansion around the gross tumor volume (GTV), which is later modified by anatomical barriers (e.g. air, non-infiltrated bone, fascia) . Some radiation oncologists use a combination of both strategies . It is worth to note, that the expansion margin also varies among radiation oncologists and treatment protocols. Kim et al. recently defined the CTV as the “third front” of radiotherapy as the field least investigated and methodologically most difficult to investigate among the target volumes .
For the visualization and delineation of structures situated in the lung parenchyma, lung window (L) is recommended and commonly used. It contrasts the soft-tissue structures against neighboring and surrounding air with higher fidelity over soft tissue window (S) . The majority of SCCHN tumors arise from the mucosa and thus there is an air interface with the tumor. However, to our knowledge there is no literature recommending or investigating the use of the L for the delineation of target volumes for SCCHN.
This work aims to investigate the geometric and dosimetric impact of two different contouring strategies based on S and L in a hypothetical ‘ideal future scenario’, where PTV would be tighter around, or preferably equal to the CTV, if the systematic and random errors can be minimized or eliminated somehow .
patient and disease characteristics
Mean age (range)
Triangular meshes (TMs) for all volumes were exported using the Eclipse Research Scripting API 13.6. An analysis-tool written in Python 3.5 was used to analyze the TMs and to calculate surfaces, volumes and Hausdorff-distances (HDs) between the two different contour sets. The Python scripts are available upon request to the corresponding author.
target volume objectives for dose coverage
D95% of PTV70
70 Gy (100%)
D5% of PTV70
≤74.9 Gy (107%)
≤77 Gy (110%)
>77 Gy (110%)
D98% of PTV70
≥66.5 Gy (95%)
≥63 Gy (90%)a
<63 Gy (90%)a
Maximum dose (hot spot ≤0.03 cm3) outside the PTV70
≤74.9 Gy (107%)
≤77 Gy (110%)
>77 Gy (110%)
To investigate any possible under-dose of the air-tumor surface, the dose coverage of CTV_L was assessed in Plan_S. Additionally, the dose coverage of CTV_Δ (CTV_L minus CTV_S) was determined. In order to quantify the dosimetric differences, OAR doses were compared among Plan_S and Plan_L.
In this study, the geometric and dosimetric differences between two target volume delineation strategies are evaluated. Thus, the statistical methodology was purely descriptive, because the differences in target volumes and dose coverage are unidirectional, where any “statistically significant” difference can be demonstrated anyway.
gross and clinical tumor volumes
Median Volume in cm3 (range)
dose coverages (%) of CTV_L and CTV_Δ on Plan_S
In this in silico analysis, a median increase of 9% in target volumes and a median three-dimensional HD close to 1 cm was observed. In over half of the cases, the CTV_Δ was covered with an inadequate dose. However, it is unknown whether this would reflect in a reduced tumor control probability (TCP) in reality. When looked at the dose coverage of the whole CTV_L and not just at the difference volume CTV_Δ, only one case (number 7 in Table 4) would receive an inadequate dose through the Plan_S.
It is worth to note, that the dosimetric results of this study, especially doses received by the OARs, do not reflect plan results of the current standards of practice, mainly due to two reasons. First, in this study CTVs instead of PTVs were used as mentioned before. Second, in order to purely investigate the plain impact of the L-based delineation strategy, any high risk nodal and elective volumes were ignored. Therefore, it is difficult to make an assumption in terms of TCP in this simulated scenario. However, the results provide an insight for extra caution possibly needed for target volume delineation for applications like single vocal cord irradiation  or stereotactic radiotherapy [11, 12], where one and relatively small target volume is used (either primary tumor or a single lymph node and without elective volumes).
It may be suggested, that the use of image registration techniques with other modalities (e.g. MRI or PET) may overcome the uncertainty whether to use S or L on CT-based volume delineation. However, such an approach causes additional problems. First of all, the image registration algorithms have more geometrical uncertainty than the difference between S and L in CT, on which the radiotherapy plan is generated. In addition to that, these imaging modalities are not free from intrinsic uncertainties caused by problems such as partial volume effect (sometimes varying among different sequences of the same MRI acquisition, for instance caused by different slice thicknesses), varying tumor appearance on MRI due to different acquisition parameters/techniques, movement artefacts (e.g. due to swallowing during MR), different neck positioning compared to planning CT or the lack of agreement over ideal thresholding on PET imaging.
Presumably, the already marginal and (in our subjective opinion) clinically negligible dose differences in OARs between Plan_S and Plan_L would be even less prominent if other high (i.e. involved lymph nodes) and low risk/elective target volumes are to be used. By looking at the overall picture, the results of this study can be interpreted towards two opposite directions. It may be argued that the extra effort to define a GTV_L and CTV_L would be trivial, since CTV to PTV margins of at least 3 mm are used. Today, less than 3-5 mm expansion margins are not recommended to generate PTV from CTV in SCCHN [13, 14], and this may blur and rule out any delineation uncertainties occurring at the air-tissue border, even though these suggested PTV margins do not take the CTV_Δ into account. In a practical sense, an increased PTV expansion based on the HDs arising from CTV_Δ would overcome this problem without increasing the L-based delineation workload. However, this would also unnecessarily enlarge the PTV towards the soft tissue, even by using anisotropic margins. Although the median HD was larger than initially expected, these geometric differences between L and S usually occur in the ‘coves’ of the concave parts of the target volumes neighboring cylindrical air cavities, which are usually engulfed by PTV margins emerging from two tips of the C-shaped volume. It is also worth to note, that using isotropic PTV expansions on CTV_L may increase the dose differences on OARs to a clinically meaningful level and increase toxicity. On the contrary, one may also argue, that the definition of these L-based target volumes does not compromise normal tissue doses in a clinically meaningful way, and poses a more systematic and accurate approach, whereas omitting it may compromise TCP, maybe not in all but some cases.
Currently, for the routine curative radiotherapy planning of SCCHN, which involves elective volumes and PTV margins, the delineation of L-based volumes seems to be trivial. However, in special settings, where smaller or no PTV margins are used, this approach may play an important role for local control.
We thank Dr. Nando Mertineit for his contribution in the discussion section.
Availability of data and materials
The datasets used and analysed during the current study are available from the corresponding author on reasonable request.
Conception and design: OE, MS, WV. Acquisition of the data and verification of their accuracy: OE, DT, MS, WV. Statistics: OE, DT, WV. Interpretation of the data: OE, DT, MS, WV, MF, PM. Drafting and critical revision of the last version of the manuscript: all co-authors. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
All patients provided written consent for the use of their medical data for research and publication.
Ethics approval and consent to participate
Ethics approval of Cantonal Review Board (Die Ethikkommission des Kantons Bern – approval number: 289/14) was obtained.
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