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International Multispecialty Journal of Health (IMJH) ISSN: [2395-6291] [Vol-3, Issue-9, September- 2017]
Page | 332
Dosimetric evaluation of carcinoma nasopharynx using
Volumetric Modulated Arc Therapy (VMAT): An institutional
experience from Western India
Dr. Upendra Nandwana1§
, Dr. Shuchita Pathak2
, Dr. TP Soni3
, T Natarajan4
,
Venugopal5
, Umra Fatima6
, Jeevraj7
1
Senior Resident, Department of Radiation Oncology, Bhagwan Mahaveer Cancer Hospital and Research Centre,
Jaipur (Rajasthan) India
2
DNB Resident, Department of Radiation Oncology, Bhagwan Mahaveer Cancer Hospital and Research Centre,
Jaipur (Rajasthan) India
3
Consultant, Department of Radiation Oncology, Bhagwan Mahaveer Cancer Hospital and Research Centre,
Jaipur (Rajasthan) India
4-7
Medical Physicist, Department of Radiation Oncology, Bhagwan Mahaveer Cancer Hospital and Research Centre,
Jaipur (Rajasthan) India
Abstract— Treatment of nasopharyngeal carcinoma is done by advanced radiotherapy techniques like
VMAT (Volumetric Modulated Arc Therapy) where dose to critical organs around tumour is of
concern. Present study aimed to describe radiation dose to critical organs in nasopharyngeal cancer
patients using VMAT technique. Study was conducted on 10 carcinoma nasopharynx patients treated by
VMAT technique at a super-specialty cancer institute in Rajasthan. The structures were contoured
using RTOG (Radiation Therapy Oncology Group) guidelines and dose prescription to PTV (Planning
Target Volume) was such that 95% iso-dose covered 100% of PTV. Constraints to the OARs (Organs at
risk) were as per QUANTEC (Quantitative Analysis of Normal Tissue Effects in the Clinic). VMAT
planning was done by double arc using Eclipse (v 10.0.42) treatment planning system. Mean dose to
brain stem, spinal cord and optic chiasma were 51.79 Gy, 45.92 Gy and 18.8 Gy respectively. Mean
dose to left and right temporal lobes was 22.7Gy and 24.3Gy. Dose to right and left eye were 20.6 Gy
and 19.2 Gy while dose to right and left lenses were 5.9Gy and 5.8 Gy respectively. Dose to brain stem,
spinal cord, optic chiasma, eyes, lens and temporal lobes were below the dose constraints. VMAT is an
effective way to deliver maximum radiation to tumour tissue while providing better sparing of normal
tissue and less doses to OARs in carcinoma nasopharynx.
Keywords: Nasopharyngeal carcinoma (NPC), Volumetric Modulated Arc Therapy, Radiation
Therapy Oncology Group.
I. INTRODUCTION
Nasopharyngeal carcinoma (NPC) is endemic in Southeast Asia region. Radiation therapy has been the
mainstay treatment of patients of nasopharyneal carcinoma. It is a curative treatment for many patients
with non metastatic NPC. It is a radiosensitive tumour but it needs complex treatment plan due to its
irregular concave shape, location and close proximity of tumour to the critical organs like spinal cord,
brain stem, salivary glands, eyes, optic nerves etc.1
In past decade significant progress has been made in field of radiotherapy delivery.1
. IMRT can provide
precise dose distribution in three dimensions. IMRT presents more conformity for irregular target
volumes close to critical organs and provides better tumor control and reduces radiation dose to nearby
normal tissue. IMRT provides better therapeutic ratio by maximizing dose to the tumour while sparing
normal tissue.2,3
In NPC, IMRT provides better dose distribution to the target volume while lower dose
to the OARs (Organs at risk).4,5
The delivery of IMRT is by a set of fixed radiation beams shaped using
International Multispecialty Journal of Health (IMJH) ISSN: [2395-6291] [Vol-3, Issue-9, September- 2017]
Page | 333
the projection of the target volume. Volumetric Modulated Arc Therapy (VMAT) is another advance in
the field of radiotherapy. It is a technique in which IMRT is given in an arc based manner with
simultaneously changing multi leaf collimator (MLC) position, gantry position, and dose rate.
This concept has been clinically used in the Eclipse treatment planning software under the name Rapid
Arc (RA).
Conventional IMRT delivers fully intensity-modulated radiotherapy fields with a multi leaf collimator
(MLC) from a finite number of fixed gantry angles, while RA delivers radiotherapy with MLC that
changes the shape of the treatment field dynamically while the gantry rotates around the patient. The
purpose of this study was to describe the dose to critical organs in nasopharynx using VMAT
technique.
II. METHODOLOGY
A dosimetric study was conducted using medical records of ten patients of nasopharyngeal cancer who
were treated with curative intent between January to July 2017. All patients underwent pretreatment
evaluation including clinical examination, imaging (MRI/CT) and pretreatment biopsy proof was done.
The tumours were staged according to the American Joint Committee on Cancer Staging System. All
patients received concurrent chemo-radiotherapy. Radiotherapy was delivered using VMAT technique
(rapid arc).VMAT plans of these ten patients were evaluated. Six out of ten patients had advanced
clinical stages (stage III/IV)
2.1 Radiotherapy
First of all planning CT scan was done with 5 clamp thermoplastic head and neck or fit with a slice
thickness of 3mm, from vertex to below the level of clavicles. Images were then transferred to
contouring workstations for contouring of target volumes and critical normal structures. Radiotherapy
was delivered with a 6MV linear accelerator using a dynamic multi leaf collimator.
The structures were contoured as per RTOG (Radiation Therapy Oncology Group) guidelines and the
dose prescription to PTV (Planning Target Volume) was such that 95% iso-dose covered 100% of the
PTV. Gross tumour volume (GTV70) included the primary tumour and any clinically involved lymph
node, taking into consideration, physical examination, nasopharyngoscopy findings, CT, PET-CT and
MRI. The clinical target volume (CTV70) was created from GTV70 by creating 0.5-1.0 cm margins.
The planning target volume (PTV70) was created from CTV by creating 5 mm margin. The CTV 54
included the entire Nasopharynx, posterior ethmoids, posterior third of nasal cavity and maxillary
sinuses, inferior sphenoid sinuses, clivus, cavernous sinuses and elective nodal areas. Neck lymph nodes
level II-IV was included in CTV54 in all cases. Dose prescription was given according to the ICRU 50
(International Commission on Radiation units and Measurements) recommendations.
Spinal cord, brain stem, optic chiasma, bilateral parotid, eyes, lens and temporal lobes were contoured
as OAR. Constraints to the OARs were as per QUANTEC (Quantitative Analysis of Normal Tissue
Effects in the Clinic). According to this, maximum dose to spinal cord and brain stem should be less
than 45 Gy and 54 Gy respectively. At least one parotid gland mean dose should be less than 26 Gy or
volume receiving 30 Gy radiations should be less than 50% of the parotid volume. The planning of all
patients was done by double arc using Eclipse treatment planning system. The dose to the critical organs
was deduced from the dose volume histogram (DVH).
Table 1 shows the dose limits for OARs.
International Multispecialty Journal of Health (IMJH) ISSN: [2395-6291] [Vol-3, Issue-9, September- 2017]
Page | 334
Table 1
Dose Constraints for OARs and End Points for Nasopharyngeal Carcinoma
Structure End point Dose (Gy) Planning Aim
Brain stem Necrosis 54 1% of the PRV should not exceed 60Gy
Brain Necrosis 60 1% of the normal brain should not exceed 60Gy
Chiasm Blindness 60 0.03cc of the chiasm should not exceed 60Gy
Spinal cord Myelitis 45 or 1cc of PRV should not exceed 50Gy
Eyes Blindness 50 Mean dose less than 50Gy
Lens Cataract 10 As low as possible
Optic nerves Blindness 54 0.03 cc should not exceed 54Gy
Mandibles Osteoradio -necrosis 70 1% of the mandible should not exceed 70Gy
Parotids Xerostomia 26 Mean dose ≤26Gy D50 should be ≤ 30 Gy for one gland
Oral Cavity
(excluding PTV)
late mucosal necrosis 40 Mean dose less than 40Gy
Unspecified Tissue 72 1cc of normal tissue outside the PTV should not receive d
not receive ≥ 110 % of PTV
*PTV-Planning Target Volume; *PRV-Planning Risk Volume; RTOG Protocol 0225
2.2 VMAT plan
Varian Rapid Arc linear accelerator, equipped with a millennium MLC with 120 leaves, was used for
treatment. Six MV photon beams were applied to treatment plans with a maximum dose rate of
600MU/min. As a part of inverse planning, the optimization process was done using PRO algorithm
(Progressive resolutive optimization).
III. RESULT
The critical structures contoured were the parotids, brain stem, spinal cord, temporal lobes, eyes, lens,
optic chiasma and optic nerves. The mean dose to the left and right parotids were 33.7 Gy and 31.4 Gy
respectively, while dose to the brain stem, spinal cord and optic chiasma were 51.79 Gy, 45.92 Gy and
18.8 Gy respectively. The mean dose to the left and right temporal lobes was 22.7Gy and 24.3Gy
respectively. The dose to right and left eye were 20.6 Gy and 19.2 Gy respectively, while dose to right
and left lenses were 5.9Gy and 5.8 Gy respectively. The dose to brain stem, spinal cord, optic chiasma,
eyes, lens and temporal lobes were below the dose constraints while the dose to parotids were above the
dose constraints probably because most (six out of ten) of these patients were advanced cases. Doses to
OARs are presented in Table 2.
Table 2
Details of dose to the organs at risk (OARs)
S. No. Organ at Risk VMAT (Gy)
1 Spinal chord Max 45.92
2 Brain stem Max 51.79
3 Parotid
R mean 33.7
L mean 31.4
4 Eye
R max 20.6
L max 19.2
5 Lens
R max 5.9
L max 5.8
6 Optic chiasm Max 18.8
7 Optic nerves
R max 28.4
L max 27
8 Temporal lobe
R mean 24.3
L mean 22.7
International Multispecialty Journal of Health (IMJH) ISSN: [2395-6291] [Vol-3, Issue-9, September- 2017]
Page | 335
IV. DISCUSSION
Radiotherapy plays an important role in local nasopharyngeal treatment. NPC patients have better
outcomes and life expectancy than other head and neck cancers. Five year survival reaches upto 85% in
early stage disease.6-8
Important point to be considered while planning for NPC is sparing of OARs as
many critical structures are in proximity to this three dimensional irregular concave shape tumour.
Advances in planning and implementation of RT have focused on delivering max dose to tumour while
sparing of surrounding critical structure. VMAT is a novel IMRT technology that has the potential of
fulfilling this aim. It allows dose rate, gantry rotation and MLC fiber velocity to be varied during
treatment.9
There are few past studies that have compared the dosimetry analysis between VMAT and IMRT in
head and neck cancer including NPC.10-12
Vanetti et al13
in a study showed that VMAT provided a better
sparing effect to OARs compared to conventional fixed field IMRT with similar target coverage in head
and neck cancers. VMAT reduced the mean dose to the contralateral parotid gland by 13.5% while the
decrement of maximal doses to the spinal cord and brain stem were 8.9% and 35.1%, respectively. In
present study VMAT was able to achieve dose limits of all OARs except for parotids. In parotid dose
limit could not be achieved due to advanced stage (III and IV) in these cases which caused close
proximity of tumour volume to parotids.
Results of present study are concordant with those presented by Zheng et al,14
where in a study of 20
patients of stage III and IV, mean dose radiation in left and right parotid was recorded to be 32.9Gy and
33.4Gy respectively. Similarly in present study the mean dose of right and left parotid were 33.7 and
31.4Gy respectively.
Limitation of present study includes smaller number of patients and difference in the patient tumour
volumes.
V. CONCLUSION
Present study supports VMAT as an effective way to deliver maximum radiation to tumour tissue while
providing better sparing of normal tissue and less doses to OARs in carcinoma nasopharynx. Further
studies with larger sample size and prospective design are required to firmly establish VMAT and its
further enhancement.
CONFLICT OF INTEREST
None declared till now.
ACKNOWLEDGEMENT
We would like to thank all the teachers of radiation oncology department and medical physicists
including T Senthil, Rajkamal and Ratish for providing their valuable support and help.
REFERENCES
[1]. Hong TS, Ritter MA, Tome WA, Harari PM. Intensity-modulated radiation therapy: emerging cancer treatment
technology.Br J Cancer 2005;92:1819-1824.
[2]. Kam MK, Chau RM, Suen J, Choi PH, Teo PM. Intensity-modulated radiotherapy in nasopharyngeal carcinoma:
dosimetric advantage over conventional plans and feasibility of dose escalation. Int J Radiat Oncol Biol Phys 2003;
56:145-157.
International Multispecialty Journal of Health (IMJH) ISSN: [2395-6291] [Vol-3, Issue-9, September- 2017]
Page | 336
[3]. Scott-Brown M, Miah A, Harrington K, Nutting C. Evidence- based review:quality of life following head and neck
intensity-modulated radiotherapy. Radiother Oncol 2010;97:249-257.
[4]. Chau RM, Teo PM, Kam MK et al. Dosimetric comparison between 2-dimensional radiation therapy andintensity
modulated radiation therapy in the treatmentof advanced T-stage nasopharyngeal carcinoma: to treat less or more in the
planning organ-at-risk volume of the brainstem and spinal cord. Med Dosim 2007;32:263-270.
[5]. Wu Q, Manning M, Schmidt-Ullrich R et al. The potential for sparing of parotids and escalation of biologically
effective dose with intensity-modulated radiation treatments of head-and-neck cancers: a treatment design study. Int J
Radiat Oncol Biol Phys 2000;46:195-205.
[6]. Xiao WW, Han F, Lu TX, Chen CY, Huang Y, Zhao C. Treatment outcomes after radiotherapy alone for patients with
early-stage nasopharyngeal carcinoma. Int J Radiat Oncol Biol Phys 2009;74:1070-1076.
[7]. Yi JL, Gao L, Huang XD et al. Nasopharyngeal carcinoma treated by radical radiotherapy alone: ten-year experience of
a single institution. Int J Radiat Oncol Biol Phys 2006;65:161-168.
[8]. Zhao C, Han F, Lu LX et al. Intensity modulated radiotherapy for local-regional advanced nasopharyngeal carcinoma.
Ai Zheng 2004;23:1532-1537.
[9]. Palma D, Vollans E, James K et al. Volumetric modulated arc therapy for delivery of prostate radiotherapy: comparison
with intensity-modulated radiotherapy and three-dimensional conformal radiotherapy. Int J Radiat Oncol Biol Phys
2008;72:996-1001.
[10]. Verbakel WF, Cuijpers JP, Hoffmans D, Bieker M, Slotman BJ, Senan S.Volumetric intensity-modulated arc therapy
vs. conventional IMRT in head and neck cancer: a comparative planning and dosimetric study. Int J Radiat Oncol Biol
Phys 2009;74:252-259.
[11]. Bertelsen A, Hansen CR, Johansen J, Brink C. Single arc volumetric modulated arc therapy of head and neck cancer.
Radiother Oncol 2010;95:142-148.
[12]. Johnston M, Clifford S, Bromley R, Back M, Oliver L, Eade T. Volumetric modulated arc therapy in head and neck
radiotherapy: a planning comparison using simultaneous integrated boost for nasopharynx and oropharynx carcinoma.
Clin Oncol (R Coll Radiol) 2011;23:503-511.
[13]. Vanetti E, Clivio A, Nicolini G et al. Volumetric modulated arc radiotherapy for carcinomas of the oro-pharynx, hypo-
pharynx and larynx: a treatment planning comparison with fixed field IMRT. Radiother Oncol 2009;92:111-117.
[14]. Zheng, et al. Dosimetry comparison between volumetric modulated arc therapy with rapidarc and fixed field dynamic
IMRT for local-regionally advanced nasopharyngeal carcinoma. Chin J Cancer Res. 2011;23(4):259–64.

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Dosimetric evaluation of carcinoma nasopharynx using Volumetric Modulated Arc Therapy (VMAT): An institutional experience from Western India

  • 1. International Multispecialty Journal of Health (IMJH) ISSN: [2395-6291] [Vol-3, Issue-9, September- 2017] Page | 332 Dosimetric evaluation of carcinoma nasopharynx using Volumetric Modulated Arc Therapy (VMAT): An institutional experience from Western India Dr. Upendra Nandwana1§ , Dr. Shuchita Pathak2 , Dr. TP Soni3 , T Natarajan4 , Venugopal5 , Umra Fatima6 , Jeevraj7 1 Senior Resident, Department of Radiation Oncology, Bhagwan Mahaveer Cancer Hospital and Research Centre, Jaipur (Rajasthan) India 2 DNB Resident, Department of Radiation Oncology, Bhagwan Mahaveer Cancer Hospital and Research Centre, Jaipur (Rajasthan) India 3 Consultant, Department of Radiation Oncology, Bhagwan Mahaveer Cancer Hospital and Research Centre, Jaipur (Rajasthan) India 4-7 Medical Physicist, Department of Radiation Oncology, Bhagwan Mahaveer Cancer Hospital and Research Centre, Jaipur (Rajasthan) India Abstract— Treatment of nasopharyngeal carcinoma is done by advanced radiotherapy techniques like VMAT (Volumetric Modulated Arc Therapy) where dose to critical organs around tumour is of concern. Present study aimed to describe radiation dose to critical organs in nasopharyngeal cancer patients using VMAT technique. Study was conducted on 10 carcinoma nasopharynx patients treated by VMAT technique at a super-specialty cancer institute in Rajasthan. The structures were contoured using RTOG (Radiation Therapy Oncology Group) guidelines and dose prescription to PTV (Planning Target Volume) was such that 95% iso-dose covered 100% of PTV. Constraints to the OARs (Organs at risk) were as per QUANTEC (Quantitative Analysis of Normal Tissue Effects in the Clinic). VMAT planning was done by double arc using Eclipse (v 10.0.42) treatment planning system. Mean dose to brain stem, spinal cord and optic chiasma were 51.79 Gy, 45.92 Gy and 18.8 Gy respectively. Mean dose to left and right temporal lobes was 22.7Gy and 24.3Gy. Dose to right and left eye were 20.6 Gy and 19.2 Gy while dose to right and left lenses were 5.9Gy and 5.8 Gy respectively. Dose to brain stem, spinal cord, optic chiasma, eyes, lens and temporal lobes were below the dose constraints. VMAT is an effective way to deliver maximum radiation to tumour tissue while providing better sparing of normal tissue and less doses to OARs in carcinoma nasopharynx. Keywords: Nasopharyngeal carcinoma (NPC), Volumetric Modulated Arc Therapy, Radiation Therapy Oncology Group. I. INTRODUCTION Nasopharyngeal carcinoma (NPC) is endemic in Southeast Asia region. Radiation therapy has been the mainstay treatment of patients of nasopharyneal carcinoma. It is a curative treatment for many patients with non metastatic NPC. It is a radiosensitive tumour but it needs complex treatment plan due to its irregular concave shape, location and close proximity of tumour to the critical organs like spinal cord, brain stem, salivary glands, eyes, optic nerves etc.1 In past decade significant progress has been made in field of radiotherapy delivery.1 . IMRT can provide precise dose distribution in three dimensions. IMRT presents more conformity for irregular target volumes close to critical organs and provides better tumor control and reduces radiation dose to nearby normal tissue. IMRT provides better therapeutic ratio by maximizing dose to the tumour while sparing normal tissue.2,3 In NPC, IMRT provides better dose distribution to the target volume while lower dose to the OARs (Organs at risk).4,5 The delivery of IMRT is by a set of fixed radiation beams shaped using
  • 2. International Multispecialty Journal of Health (IMJH) ISSN: [2395-6291] [Vol-3, Issue-9, September- 2017] Page | 333 the projection of the target volume. Volumetric Modulated Arc Therapy (VMAT) is another advance in the field of radiotherapy. It is a technique in which IMRT is given in an arc based manner with simultaneously changing multi leaf collimator (MLC) position, gantry position, and dose rate. This concept has been clinically used in the Eclipse treatment planning software under the name Rapid Arc (RA). Conventional IMRT delivers fully intensity-modulated radiotherapy fields with a multi leaf collimator (MLC) from a finite number of fixed gantry angles, while RA delivers radiotherapy with MLC that changes the shape of the treatment field dynamically while the gantry rotates around the patient. The purpose of this study was to describe the dose to critical organs in nasopharynx using VMAT technique. II. METHODOLOGY A dosimetric study was conducted using medical records of ten patients of nasopharyngeal cancer who were treated with curative intent between January to July 2017. All patients underwent pretreatment evaluation including clinical examination, imaging (MRI/CT) and pretreatment biopsy proof was done. The tumours were staged according to the American Joint Committee on Cancer Staging System. All patients received concurrent chemo-radiotherapy. Radiotherapy was delivered using VMAT technique (rapid arc).VMAT plans of these ten patients were evaluated. Six out of ten patients had advanced clinical stages (stage III/IV) 2.1 Radiotherapy First of all planning CT scan was done with 5 clamp thermoplastic head and neck or fit with a slice thickness of 3mm, from vertex to below the level of clavicles. Images were then transferred to contouring workstations for contouring of target volumes and critical normal structures. Radiotherapy was delivered with a 6MV linear accelerator using a dynamic multi leaf collimator. The structures were contoured as per RTOG (Radiation Therapy Oncology Group) guidelines and the dose prescription to PTV (Planning Target Volume) was such that 95% iso-dose covered 100% of the PTV. Gross tumour volume (GTV70) included the primary tumour and any clinically involved lymph node, taking into consideration, physical examination, nasopharyngoscopy findings, CT, PET-CT and MRI. The clinical target volume (CTV70) was created from GTV70 by creating 0.5-1.0 cm margins. The planning target volume (PTV70) was created from CTV by creating 5 mm margin. The CTV 54 included the entire Nasopharynx, posterior ethmoids, posterior third of nasal cavity and maxillary sinuses, inferior sphenoid sinuses, clivus, cavernous sinuses and elective nodal areas. Neck lymph nodes level II-IV was included in CTV54 in all cases. Dose prescription was given according to the ICRU 50 (International Commission on Radiation units and Measurements) recommendations. Spinal cord, brain stem, optic chiasma, bilateral parotid, eyes, lens and temporal lobes were contoured as OAR. Constraints to the OARs were as per QUANTEC (Quantitative Analysis of Normal Tissue Effects in the Clinic). According to this, maximum dose to spinal cord and brain stem should be less than 45 Gy and 54 Gy respectively. At least one parotid gland mean dose should be less than 26 Gy or volume receiving 30 Gy radiations should be less than 50% of the parotid volume. The planning of all patients was done by double arc using Eclipse treatment planning system. The dose to the critical organs was deduced from the dose volume histogram (DVH). Table 1 shows the dose limits for OARs.
  • 3. International Multispecialty Journal of Health (IMJH) ISSN: [2395-6291] [Vol-3, Issue-9, September- 2017] Page | 334 Table 1 Dose Constraints for OARs and End Points for Nasopharyngeal Carcinoma Structure End point Dose (Gy) Planning Aim Brain stem Necrosis 54 1% of the PRV should not exceed 60Gy Brain Necrosis 60 1% of the normal brain should not exceed 60Gy Chiasm Blindness 60 0.03cc of the chiasm should not exceed 60Gy Spinal cord Myelitis 45 or 1cc of PRV should not exceed 50Gy Eyes Blindness 50 Mean dose less than 50Gy Lens Cataract 10 As low as possible Optic nerves Blindness 54 0.03 cc should not exceed 54Gy Mandibles Osteoradio -necrosis 70 1% of the mandible should not exceed 70Gy Parotids Xerostomia 26 Mean dose ≤26Gy D50 should be ≤ 30 Gy for one gland Oral Cavity (excluding PTV) late mucosal necrosis 40 Mean dose less than 40Gy Unspecified Tissue 72 1cc of normal tissue outside the PTV should not receive d not receive ≥ 110 % of PTV *PTV-Planning Target Volume; *PRV-Planning Risk Volume; RTOG Protocol 0225 2.2 VMAT plan Varian Rapid Arc linear accelerator, equipped with a millennium MLC with 120 leaves, was used for treatment. Six MV photon beams were applied to treatment plans with a maximum dose rate of 600MU/min. As a part of inverse planning, the optimization process was done using PRO algorithm (Progressive resolutive optimization). III. RESULT The critical structures contoured were the parotids, brain stem, spinal cord, temporal lobes, eyes, lens, optic chiasma and optic nerves. The mean dose to the left and right parotids were 33.7 Gy and 31.4 Gy respectively, while dose to the brain stem, spinal cord and optic chiasma were 51.79 Gy, 45.92 Gy and 18.8 Gy respectively. The mean dose to the left and right temporal lobes was 22.7Gy and 24.3Gy respectively. The dose to right and left eye were 20.6 Gy and 19.2 Gy respectively, while dose to right and left lenses were 5.9Gy and 5.8 Gy respectively. The dose to brain stem, spinal cord, optic chiasma, eyes, lens and temporal lobes were below the dose constraints while the dose to parotids were above the dose constraints probably because most (six out of ten) of these patients were advanced cases. Doses to OARs are presented in Table 2. Table 2 Details of dose to the organs at risk (OARs) S. No. Organ at Risk VMAT (Gy) 1 Spinal chord Max 45.92 2 Brain stem Max 51.79 3 Parotid R mean 33.7 L mean 31.4 4 Eye R max 20.6 L max 19.2 5 Lens R max 5.9 L max 5.8 6 Optic chiasm Max 18.8 7 Optic nerves R max 28.4 L max 27 8 Temporal lobe R mean 24.3 L mean 22.7
  • 4. International Multispecialty Journal of Health (IMJH) ISSN: [2395-6291] [Vol-3, Issue-9, September- 2017] Page | 335 IV. DISCUSSION Radiotherapy plays an important role in local nasopharyngeal treatment. NPC patients have better outcomes and life expectancy than other head and neck cancers. Five year survival reaches upto 85% in early stage disease.6-8 Important point to be considered while planning for NPC is sparing of OARs as many critical structures are in proximity to this three dimensional irregular concave shape tumour. Advances in planning and implementation of RT have focused on delivering max dose to tumour while sparing of surrounding critical structure. VMAT is a novel IMRT technology that has the potential of fulfilling this aim. It allows dose rate, gantry rotation and MLC fiber velocity to be varied during treatment.9 There are few past studies that have compared the dosimetry analysis between VMAT and IMRT in head and neck cancer including NPC.10-12 Vanetti et al13 in a study showed that VMAT provided a better sparing effect to OARs compared to conventional fixed field IMRT with similar target coverage in head and neck cancers. VMAT reduced the mean dose to the contralateral parotid gland by 13.5% while the decrement of maximal doses to the spinal cord and brain stem were 8.9% and 35.1%, respectively. In present study VMAT was able to achieve dose limits of all OARs except for parotids. In parotid dose limit could not be achieved due to advanced stage (III and IV) in these cases which caused close proximity of tumour volume to parotids. Results of present study are concordant with those presented by Zheng et al,14 where in a study of 20 patients of stage III and IV, mean dose radiation in left and right parotid was recorded to be 32.9Gy and 33.4Gy respectively. Similarly in present study the mean dose of right and left parotid were 33.7 and 31.4Gy respectively. Limitation of present study includes smaller number of patients and difference in the patient tumour volumes. V. CONCLUSION Present study supports VMAT as an effective way to deliver maximum radiation to tumour tissue while providing better sparing of normal tissue and less doses to OARs in carcinoma nasopharynx. Further studies with larger sample size and prospective design are required to firmly establish VMAT and its further enhancement. CONFLICT OF INTEREST None declared till now. ACKNOWLEDGEMENT We would like to thank all the teachers of radiation oncology department and medical physicists including T Senthil, Rajkamal and Ratish for providing their valuable support and help. REFERENCES [1]. Hong TS, Ritter MA, Tome WA, Harari PM. Intensity-modulated radiation therapy: emerging cancer treatment technology.Br J Cancer 2005;92:1819-1824. [2]. Kam MK, Chau RM, Suen J, Choi PH, Teo PM. Intensity-modulated radiotherapy in nasopharyngeal carcinoma: dosimetric advantage over conventional plans and feasibility of dose escalation. Int J Radiat Oncol Biol Phys 2003; 56:145-157.
  • 5. International Multispecialty Journal of Health (IMJH) ISSN: [2395-6291] [Vol-3, Issue-9, September- 2017] Page | 336 [3]. Scott-Brown M, Miah A, Harrington K, Nutting C. Evidence- based review:quality of life following head and neck intensity-modulated radiotherapy. Radiother Oncol 2010;97:249-257. [4]. Chau RM, Teo PM, Kam MK et al. Dosimetric comparison between 2-dimensional radiation therapy andintensity modulated radiation therapy in the treatmentof advanced T-stage nasopharyngeal carcinoma: to treat less or more in the planning organ-at-risk volume of the brainstem and spinal cord. Med Dosim 2007;32:263-270. [5]. Wu Q, Manning M, Schmidt-Ullrich R et al. The potential for sparing of parotids and escalation of biologically effective dose with intensity-modulated radiation treatments of head-and-neck cancers: a treatment design study. Int J Radiat Oncol Biol Phys 2000;46:195-205. [6]. Xiao WW, Han F, Lu TX, Chen CY, Huang Y, Zhao C. Treatment outcomes after radiotherapy alone for patients with early-stage nasopharyngeal carcinoma. Int J Radiat Oncol Biol Phys 2009;74:1070-1076. [7]. Yi JL, Gao L, Huang XD et al. Nasopharyngeal carcinoma treated by radical radiotherapy alone: ten-year experience of a single institution. Int J Radiat Oncol Biol Phys 2006;65:161-168. [8]. Zhao C, Han F, Lu LX et al. Intensity modulated radiotherapy for local-regional advanced nasopharyngeal carcinoma. Ai Zheng 2004;23:1532-1537. [9]. Palma D, Vollans E, James K et al. Volumetric modulated arc therapy for delivery of prostate radiotherapy: comparison with intensity-modulated radiotherapy and three-dimensional conformal radiotherapy. Int J Radiat Oncol Biol Phys 2008;72:996-1001. [10]. Verbakel WF, Cuijpers JP, Hoffmans D, Bieker M, Slotman BJ, Senan S.Volumetric intensity-modulated arc therapy vs. conventional IMRT in head and neck cancer: a comparative planning and dosimetric study. Int J Radiat Oncol Biol Phys 2009;74:252-259. [11]. Bertelsen A, Hansen CR, Johansen J, Brink C. Single arc volumetric modulated arc therapy of head and neck cancer. Radiother Oncol 2010;95:142-148. [12]. Johnston M, Clifford S, Bromley R, Back M, Oliver L, Eade T. Volumetric modulated arc therapy in head and neck radiotherapy: a planning comparison using simultaneous integrated boost for nasopharynx and oropharynx carcinoma. Clin Oncol (R Coll Radiol) 2011;23:503-511. [13]. Vanetti E, Clivio A, Nicolini G et al. Volumetric modulated arc radiotherapy for carcinomas of the oro-pharynx, hypo- pharynx and larynx: a treatment planning comparison with fixed field IMRT. Radiother Oncol 2009;92:111-117. [14]. Zheng, et al. Dosimetry comparison between volumetric modulated arc therapy with rapidarc and fixed field dynamic IMRT for local-regionally advanced nasopharyngeal carcinoma. Chin J Cancer Res. 2011;23(4):259–64.