- Open Access
Submandibular gland-sparing radiation therapy for locally advanced oropharyngeal squamous cell carcinoma: patterns of failure and xerostomia outcomes
Radiation Oncologyvolume 9, Article number: 255 (2014)
Saliva from submandibular glands (SMG) is necessary to minimize xerostomia. It is unclear whether SMG can be safely spared in patients undergoing bilateral neck radiotherapy for locally advanced oropharyngeal cancer without increasing the risk of marginal recurrence. We evaluated the outcomes of contralateral submandibular gland (cSMG) sparing intensity-modulated radiation therapy (IMRT).
All patients with stage III/IV oropharyngeal squamous cell carcinoma treated with bilateral neck IMRT from 2006–2012 at our institution were included. Appropriately selected patients with favorable primary tumor characteristics and no definite contralateral neck disease were treated with cSMG-sparing IMRT. Patterns of failure and xerostomia outcomes were retrospectively analyzed.
114 patients were treated. 89% had stage IV disease and 89% received definitive radiation therapy. 76 patients (67%) received cSMG sparing IMRT. With a median follow-up of 30 months, there were 10 local, 9 regional, and 10 distant recurrences. 2-year overall survival was 86% and 2-year loco-regional control was 87%. In cSMG spared patients, the mean cSMG dose was 30.7 Gy. Late grade 2+ xerostomia was significantly reduced in the cSMG spared group compared to those without SMG sparing (6 months: 23% vs. 72%, 12 months: 6% vs. 41%, 24 months: 3% vs. 36%, all p < 0.0007). There were no peri-SMG marginal recurrences in the cSMG-spared cohort.
cSMG sparing IMRT did not increase marginal failures in this series of locally advanced oropharyngeal SCC patients. Xerostomia was significantly reduced in cSMG spared patients.
Oropharyngeal squamous cell cancer (OSCC) patients treated with radiotherapy (RT) are often cured of their disease . However, chronic xerostomia remains a vexing and common clinical problem that impairs the quality of life of surviving patients. Sparing of salivary glands is essential to minimize xerostomia . Parotid-sparing intensity-modulated radiation therapy (IMRT) is a standard radiotherapy technique for patients with squamous cancers of the head and neck region -. However, parotid saliva lacks mucins that maintain a patient’s subjective sense of hydration, and preserving the parotids alone has inconsistently translated to improvements in xerostomia -. Randomized studies comparing parotid-sparing IMRT with non-parotid-sparing techniques reported that despite better salivary flow rates with IMRT, the improvement in patient-reported xerostomia scores were modest -. One study demonstrated that the advantage of parotid sparing after therapy was <10 points on a 0–100 scale at one year, and regarded this difference as clinically insignificant . Thus, parotid-sparing IMRT may be inadequate for maximizing patient-related xerostomia outcomes.
The submandibular glands (SMGs) contribute 65-90% of unstimulated saliva and account for almost 95% of salivary flow during a 24-hour period; this saliva is rich in mucins ,,. It has been reported that restricting the mean dose in one SMG to less than 39 Gy improved salivary flow and correlated with favorable rates of patient- and observer-rated xerostomia ,.
In patients treated with RT for a locally advanced oropharyngeal SCC, it is seldom possible to spare the ipsilateral SMG as it directly abuts the primary tumor and/or grossly involved lymph nodes that are treated to a tumoricidal dose of 66–70 Gy. However, it might be possible to spare the contralateral SMG (cSMG) since the level 1B nodes that lie anterior to the gland rarely harbor metastases from OSCC -. While it may be desirable to spare the cSMG, this is technically demanding due to its anatomical location in close proximity to levels II and III jugulodigastric nodal regions that are electively targeted during the treatment of advanced OSCC ,. A primary OSCC that crosses the midline can also makes cSMG sparing difficult. Sparing of the cSMG is further hindered by the gland’s relatively small size. A treatment planning study of cSMG-sparing IMRT reported that in order to reduce the mean cSMG dose from 54 Gy to 40 Gy it was necessary to accept an under-dosage of target volumes in the vicinity of the gland to 90% of prescribed dose . Due to these challenges, there are concerns that cSMG sparing IMRT could compromise dose to the adjacent target volumes in levels II and III and/or the primary tumor, leading to an increased risk of marginal recurrences ,.
There are no randomized trials evaluating the clinical outcomes of cSMG-sparing IMRT. Two small reports have compared the effectiveness of cSMG-sparing IMRT with non-SMG sparing IMRT ,. While both groups found an improvement in xerostomia with cSMG sparing, the small sample sizes of 26 and 18 cSMG-spared patients make it difficult to rule out an increased marginal recurrence rate from cSMG sparing. Moreover, both series included patients with a variety of primary tumor sites, which could complicate their interpretation. Thus, it is unclear whether the cSMG could be spared to reduce long term xerostomia, without increasing the risk of a local-regional recurrence in patients with locally advanced oropharyngeal SCC requiring bilateral neck RT.
In mid-2006, at the University of Washington we commenced a policy of cSMG sparing IMRT, in addition to standard parotid sparing for the treatment of suitable OSCC patients. We report the outcomes in patients with locally advanced OSCC treated with bilateral neck IMRT at our institution. We divided the patients into cSMG-spared and cSMG-unspared groups in order to compare the incidence of peri-SMG marginal failures and xerostomia.
Materials and methods
Institutional Review Board approval was obtained for this retrospective review of patients treated with IMRT for advanced OSCC.
We identified all patients with stage III/IV OSCC treated with bilateral neck IMRT at our institution between 2006–2012. Patients treated for recurrent disease or early stage (stage I/II) disease, and those receiving unilateral treatment for well-lateralized tumors (e.g. early tonsil primaries) were excluded to minimize population heterogeneity. Six patients were excluded for short follow-up of <6 months.
For analysis of cSMG-sparing comparative outcomes, patients were divided into two groups, defined as follows: 1) cSMG spared: contralateral level IB nodal level was not targeted for elective RT and cSMG had an IMRT planning objective. 2) cSMG unspared: all other patients. Patients with nodal involvement limited to the unilateral neck and who had an anatomically favorable primary tumor were considered for cSMG sparing. Contraindications included a primary tumor extending close to the cSMG due to risk of under-dosing the tumor, or primary tumor involvement of the contralateral oral cavity, which would place the level IB space at risk.
Staging and surveillance
Patients were staged per standard NCCN guidelines. PET or MRI scans were used as clinically indicated. Surveillance was every 3–4 monthly for 2–3 years, with increasing follow up intervals thereafter. Neck dissections were reserved for an incomplete response at >3 months or for progressive disease.
Unless there was low neck involvement, patients were treated with “split field” technique with multi-beam static IMRT to the primary and upper neck matched with a supraclavicular AP field using Elekta (Stockholm, Sweden) treatment machines and Pinnacle (Best, Netherlands) planning system. Nodal levels were defined per RTOG guidelines. A simultaneous integrated boost method was used. In patients with gross disease, the highest risk target volume (PTV1) was prescribed 70 Gy in 33 fractions; the intermediate and low risk subclinical volumes (PTV2 and PTV3) received 62.7 and 57 Gy, respectively. Two patients received a concomitant boost regimen. Patients treated postoperatively were prescribed 60, 57 and 54 Gy in 30 fractions to PTV1, PTV2, and PTV3. Regions harboring close or positive margins and/or extracapsular nodal spread were boosted to 63–66 Gy. In order to maximize salivary sparing, for PTV3, CTV to PTV expansion was limited to 2–5 mm. Although we covered level II adequately, the anterior extent of PTV3 contours were restricted to the great vessels (Figure 1). The contours of all cases were prospectively quality assured by 2 clinicians (UP & JJL), prior to dosimetric planning.
PTVs were covered by the 95% isodose line, although 90-95% coverage was accepted for PTV3 to optimize SMG sparing. SMG dose was pushed as low as possible without compromising coverage of PTV1 and PTV2. When possible, bilateral parotid glands were spared to achieve mean dose <24 Gy. Spinal cord with a 5 mm margin was limited to <45 Gy.
Patient positioning was verified with weekly MV port films or kV cone-beam CT. There was increasing utilization of daily cone-beam CT since its implementation in 2010.
Kaplan-Meier overall survival, disease-free survival and loco-regional control were calculated. Event times for death/recurrence were calculated from the first day of RT. For disease-free survival calculations, events were recurrence and/or death. Viable tumor cells at time of salvage neck dissection were counted as a regional failure. Baseline characteristics were compared between the cSMG-spared and unspared groups using Fisher’s exact test and Wilcoxon rank sum test. Calculations were done with the statistical software R, version 3.0.2 (University of Auckland).
We recorded dosimetric parameters to determine target coverage. V93% (volume of target receiving at least 93% of prescribed dose) and D95% (minimum dose received by 95% of target volume) were recorded per RTOG 1216 . Mean doses to cSMG and both parotids were recorded.
Definition of “peri-cSMG” recurrence
In order to identify recurrences potentially attributable to SMG sparing, peri-cSMG recurrences were defined as any regional nodal relapse in levels I/II/III on the side of the cSMG, or primary tumor recurrence within 2 cm of the cSMG.
Late toxicity was retrospectively scored using the Common Terminology Criteria for Adverse Events version 4 . Late toxicity was defined as occurring 6 months or more after the last day of RT. Grades of xerostomia were recorded. Factors predictive of late xerostomia were explored using univariate and multivariate logistic regression.
In total, 114 patients were treated. The patient characteristics are listed in Table 1. Seventy-six patients (67%) had cSMG sparing and 38 had non-cSMG-sparing IMRT. Eighty-nine percent of patients had stage IV disease. Eighty-nine percent of patients had definitive RT and 11% had post-operative adjuvant RT. Median highest prescribed dose was 70 Gy in 33 fractions (range 60–72 Gy). 89% received concurrent systemic therapy, most commonly cisplatin on a three weekly cycle. Fifteen percent of patients underwent consolidation neck dissection <6 months following definitive RT.
Median follow-up in surviving patients was 30 months (range 8–86). Twenty patients have died. Twenty-three patients developed recurrent disease. Ten patients had disease recurrence in the primary site, nine in the regional nodes and ten in distant sites. Table 2 lists patterns of failure by treatment group. Two-year overall survival was 86%, 2-year disease-free survival was 77%, and 2-year locoregional control was 87% (Figure 2).
Forty-eight patients were tested for HPV status based on either p16 immunohistochemistry or HPV DNA probe, and forty-two were positive. Of the sixty-six patients with unknown HPV/p16 status, thirty-five had fewer than 20 pack-years smoking history, which suggests that their cancers were likely to be HPV-associated .
cSMG spared group: planning dosimetry and disease outcomes
Among the 76 patients who received cSMG sparing treatment, 87% had stage IV disease and 43% had T3/T4 tumors. 54% had tonsil and 42% had tongue base primaries. 86% had definitive RT.
The mean cSMG dose was 30.7 Gy (range 15.6-56.2). Mean cSMG dose <39 Gy and <50 Gy were achieved in sixty-two (82%) and seventy-two (95%) patients, respectively. The mean parotid dose on the SMG-spared side was 22.5 Gy (range 12.8-33.3).
Target PTV dosimetric coverage was not compromised by cSMG sparing. For PTV3 on the SMG-spared side, 72/76 of patients had V93% within the RTOG 1216 acceptable range of >/=97% of PD and 68/76 had D95% within the acceptable range of 95-107% of PD. Median V93% was 99% and median D95% was 100%.
At a median follow-up of 26 months, 64 patients are alive and 12 have died. Thirteen patients developed recurrent disease. Seven patients had disease recurrence in the primary site, five in the regional nodes and four in distant sites. Of the seven patients with primary site recurrences, none recurred within 2 cm of a spared SMG. Of the five patients with nodal recurrence, four had disease recurrence on the initial side of disease involvement. Only one patient had nodal disease recurrence on the side of a spared SMG, but disease recurred in level IV. Thus, there were no peri-SMG recurrences attributable to cSMG sparing IMRT. 2-year Kaplan-Meier overall survival was 88%; 2-year disease-free survival was 79% and 2-year locoregional control was 88%.
cSMG unspared group
In thirty-eight patients, no attempt was made to spare the cSMG. Compared to the cSMG spared group, these patients were more likely to have T4 tumors (odds ratio 2.7, p = 0.02) and contralateral neck disease (odds ratio 18.8, p < 0.0001). While mean parotid gland dose was similar between the cSMG spared and unspared groups (32.1 vs. 34.4 Gy, p = 0.17), contralateral parotid dose was lower in the cSMG spared group (mean 22.5 vs. 27.8 Gy, p < 0.0001). We classified cSMG unspared patients into two groups indicating why the cSMG was not spared: 1) Twenty-six had no planning objective to spare the cSMG, due to contralateral neck disease (n = 21) or large primary tumors extending in close proximity to the cSMG (n = 5). 2) Twelve patients had elective targeting of the contralateral level IB nodal level due to significant extension of primary tumor into the oral tongue.
10/38 patients developed recurrent disease. Three patients had disease recurrence in the primary site, four in the regional nodes and six in distant sites. Of the 38 patients, only one had a recurrence near an unspared cSMG. This patient had a T4bN2c tumor and developed a contralateral level IIA recurrence centrally within the high dose volume. There was no planning objective to spare the cSMG in this case and the mean cSMG dose was 68 Gy. This patient also had synchronous distant metastases along with multiple sites of regional failure.
Xerostomia data at 6, 12, and 24 months after completion of RT were available for 94, 81, and 62 patients, respectively. Late grade 2+ xerostomia was significantly reduced in the cSMG spared group compared to those without SMG sparing (6 months: 23% vs. 72%, 12 months: 6% vs. 41%, 24 months: 3% vs. 36%, all p < 0.0007; Figure 3, Table 3). There was a positive correlation between cSMG mean dose and incidence of grade 2+ xerostomia at 6 months for the entire cohort of 114 patients (Figure 4). Because of the potential for confounders such as parotid gland dose, univariate and multivariate logistic regression predicting grade 2+ xerostomia at 6 months was performed (Table 4). Covariates were cSMG dose, contralateral parotid dose, T4 vs. T1-3 tumors, tongue base vs. other primary sites, bilateral vs. unilateral nodal disease, concurrent systemic therapy, and age at treatment. On univariate analysis, cSMG dose, contralateral parotid dose, T4 tumor, and presence of bilateral nodal disease were all positively correlated with xerostomia. On multivariate analysis, only cSMG dose (OR = 1.07 (1.02-1.11) per Gy, p = 0.002) and T4 tumor (OR = 3.90 (1.10-14.95), p = 0.04) were predictive of xerostomia. Mean bilateral parotid dose was analyzed as well and was not a significant predictor of xerostomia on univariate analysis (OR 1.03 (0.97-1.09), p = 0.31) or multivariate analysis (OR 0.99 (0.91-1.07), p = 0.75).
While parotid-sparing IMRT improves salivary flow rates and is considered the standard technique for treating patients with locally advanced OSCC, it may be inadequate for patient-rated xerostomia, which has a significant adverse impact on quality of life ,,,. To further diminish the negative consequences of xerostomia, in 2006 we began a program to spare the contralateral submandibular gland (cSMG) in patients with locally advanced oropharyngeal cancer without contralateral nodal involvement, and who had an anatomically suitable primary tumor. In 76 patients treated with cSMG sparing bilateral neck IMRT, we were able to limit the cSMG mean dose to 30.7 Gy. Xerostomia was significantly lower in the cSMG spared group compared to the unspared group, independent of parotid sparing. The magnitude of benefit from cSMG sparing seen in this study is notable. The PARSPORT randomized trial is the largest reported study comparing parotid sparing versus non-salivary sparing radiation therapy in oropharyngeal cancer patients . In that study, parotid sparing resulted in a 25% absolute reduction in RTOG grade 2+ xerostomia at 12 months. By contrast, in the present study cSMG sparing resulted in a 35% reduction in grade 2+ xerostomia at 12 months. This benefit was durable, with reduction in xerostomia also seen at the 24 month time point. While these findings could be influenced by differences in patient characteristics between the cSMG-spared and unspared groups, the strong influence of cSMG dose on xerostomia persisted on multivariate analysis.
This is the largest report comparing outcomes from cSMG-sparing and non-cSMG sparing IMRT. Two smaller studies have been reported ,. Saarilahti et al. reported on 18 patients treated with cSMG-sparing IMRT and compared their outcomes with 18 patients who did not have SMG sparing. Xerostomia was reduced in the SMG-spared group and there were no recurrences detected in the vicinity of the spared SMG. The SMG spared group had 8 patients with advanced stage OSCC. This series was subsequently updated with more patients, but without a comparative group . Wang et al. reported that xerostomia at 6 months post-treatment was significantly improved among 26 patients treated with cSMG-sparing IMRT compared to 26 patients who received non-cSMG sparing IMRT. However, this difference did not persist at a longer follow up of 12 and 18 months . There was one level II nodal failure in each group. Only five of their cSMG-spared patients had advanced stage OSCC. With the large sample size of >100 patients in the present study and the durable improvement seen in xerostomia, this report adds valuable information on the outcomes of cSMG-sparing IMRT in oropharynx cancer.
There are concerns that aggressive cSMG sparing could compromise adequate coverage of target volumes, with an increased risk of marginal recurrences ,. Consequences of a marginal miss could be disastrous -. For example, peri-parotid recurrences have been observed in patients who had aggressive parotid sparing . In order to maximize cSMG sparing, we included the great vessels of the neck (internal carotid and jugular) but not the region immediately posterior to the gland in the elective PTV (Figure 1). This represents a modification from the existing RTOG contouring guidelines . Our definition of peri-SMG marginal recurrences was expected to be broad in identifying any failures that may have resulted as a consequence of SMG sparing. The lack of marginal relapses in the 76 cSMG spared patients with a median follow up of 26 months is reassuring. Since most recurrences in OSCC occur within 2–3 years after radiation therapy, the observed disease control rate should be maintained well over time.
There are other series reporting on the patterns of failure following cSMG-sparing IMRT for OSCC, although they did not have a cSMG unspared group to compare xerostomia outcomes (Table 5). The largest of these included 50 stage I-IV OSCC patients treated at Helsinki University Hospital along with 30 patients with other primary tumor locations. There were no recurrences in nodal levels I, II or the “vicinity” of the spared gland . Other smaller series report similar outcomes ,,. Taken together, these experiences with over 150 patients demonstrate that cSMG sparing for oropharynx SCC patients can be achieved without increasing the risk of marginal failures. However, patient selection is crucial and we caution against sparing the cSMG when a large and infiltrative primary cancer extends in close proximity to the cSMG.
A limitation of our study is the retrospective, non-randomized design. There were known differences between the cSMG spared and unspared groups; for instance, there were more T4 tumors (47% vs 25%) in the unspared group. Although T4 stage was a significant predictor of worse xerostomia (p = 0.04), cSMG dose remained the strongest predictor (p = 0.002) in the multivariate analysis. We did not record objective salivary flow measurements or perform formal quality of life questionnaires. However, the observed clinical benefits of SMG sparing and the relationship between SMG dose and function in our series are consistent with the published literature ,,,.
For patients with locally advanced OSCC, cSMG sparing is feasible in the majority of patients and may be safely attempted on the side of the neck being planned for elective nodal irradiation to reduce xerostomia and improve quality of life. The reduction in xerostomia in this series was large and clinically meaningful. In the absence of a randomized controlled study these observational data may be of value to clinicians considering cSMG-sparing IMRT for OSCC.
Parvathaneni U, Laramore GE, Liao JJ: Technical advances and pitfalls in head and neck radiotherapy. J Oncol. 2012, 2012: 597467-10.1155/2012/597467.
Nutting CM, Morden JP, Harrington KJ, Urbano TG, Bhide SA, Clark C, Miles EA, Miah AB, Newbold K, Tanay M, Adab F, Jefferies SJ, Scrase C, Yap BK, A’Hern RP, Sydenham MA, Emson M, Hall E: Parotid-sparing intensity modulated versus conventional radiotherapy in head and neck cancer (PARSPORT): a phase 3 multicentre randomised controlled trial. Lancet Oncol. 2011, 12: 127-136. 10.1016/S1470-2045(10)70290-4.
Pow EHN, Kwong DLW, McMillan AS, Wong MC, Sham JS, Leung LH, Leung WK: Xerostomia and quality of life after intensity-modulated radiotherapy vs. conventional radiotherapy for early-stage nasopharyngeal carcinoma: initial report on a randomized controlled clinical trial. Int J Radiat Oncol Biol Phys. 2006, 66: 981-991. 10.1016/j.ijrobp.2006.06.013.
Kam MKM, Leung S, Zee B, Chau RM, Suen JJ, Mo F, Lai M, Ho R, Cheung KY, Yu BK, Chiu SK, Choi PH, Teo PM, Kwan WH, Chan AT: Prospective randomized study of intensity-modulated radiotherapy on salivary gland function in early-stage nasopharyngeal carcinoma patients. J Clin Oncol. 2007, 25: 4873-4879. 10.1200/JCO.2007.11.5501.
Gupta T, Agarwal J, Jain S, Phurailatpam R, Kannan S, Ghosh-Laskar S, Murthy V, Budrukkar A, Dinshaw K, Prabhash K, Chaturvedi P, D’Cruz A: Three-dimensional conformal radiotherapy (3D-CRT) versus intensity modulated radiation therapy (IMRT) in squamous cell carcinoma of the head and neck: a randomized controlled trial. Radiother Oncol. 2012, 104: 343-348. 10.1016/j.radonc.2012.07.001.
Eisbruch A, Kim HM, Terrell JE, Marsh LH, Dawson LA, Ship JA: Xerostomia and its predictors following parotid-sparing irradiation of head-and-neck cancer. Int J Radiat Oncol Biol Phys. 2001, 50: 695-704. 10.1016/S0360-3016(01)01512-7.
Tabak LA: In defense of the oral cavity: structure, biosynthesis, and function of salivary mucins. Annu Rev Physiol. 1995, 57: 547-564. 10.1146/annurev.ph.57.030195.002555.
Eisbruch A: Reducing xerostomia by IMRT: what may, and may not, be achieved. J Clin Oncol. 2007, 25: 4863-4864. 10.1200/JCO.2007.13.4874.
Jellema AP, Slotman BJ, Doornaert P, Leemans CR, Langendijk JA: Impact of radiation induced xerostomia on quality of life after primary radiotherapy among patients with head and neck cancer. Int J Radiat Oncol Biol Phys. 2007, 69: 751-760. 10.1016/j.ijrobp.2007.04.021.
Meirovitz A, Murdoch-Kinch CA, Schipper M, Pan C, Eisbruch A: Grading xerostomia by physicians or by patients after IMRT of head and neck cancer. Int J Radiat Oncol Biol Phys. 2006, 66: 445-453. 10.1016/j.ijrobp.2006.05.002.
Lavelle CLB: Applied Physiology of the Mouth. 1975, John Wright and Sons, Bristol
Murdoch-Kinch CA, Kim HM, Vineberg KA, Ship JA, Eisbruch A: Dose-effect relationships for the submandibular salivary glands and implications for their sparing by intensity modulated radiotherapy. Int J Radiat Oncol Biol Phys. 2008, 722: 373-382. 10.1016/j.ijrobp.2007.12.033.
Little M, Schipper M, Feng FY, Vineberg K, Cornwall C, Murdoch-Kinch CA, Eisbruch A: Reducing xerostomia after chemo-IMRT for head-and-neck cancer: beyond sparing the parotid glands. Int J Radiat Oncol Biol Phys. 2012, 83: 1007-1014. 10.1016/j.ijrobp.2011.09.004.
Mendenhall WM, Mendenhall CM, Mendenhall NP: Submandibular gland-sparing intensity-modulated radiotherapy. Am J Clin Oncol in press.,
Sanguinetti G, Califano J, Stafford E, Fox J, Koch W, Tufano R, Sormani MP, Forastiere A: Defining the risk of involvement for each neck nodal level in patients with early T-stage node-positive oropharyngeal carcinoma. Int J Radiat Oncol Biol Phys. 2009, 74: 1356-1364. 10.1016/j.ijrobp.2008.10.018.
Lindberg R: Distribution of cervical lymph node metastases from squamous cell carcinoma of the upper respiratory and digestive tracts. Cancer. 1972, 29: 1446-1449. 10.1002/1097-0142(197206)29:6<1446::AID-CNCR2820290604>3.0.CO;2-C.
Jang JW, Parambi RJ, Liliana LS, Liebsch NJ, Chan AW: Intensity modulated radiation therapy and level 1B nodal coverage for oropharyngeal carcinoma. Int J Radiat Oncol Biol Phys. 2012, 84: S22-S23. 10.1016/j.ijrobp.2012.07.064.
Houweling AC, Dijkema T, Roesink JM, Terhaard CH, Raaijmakers CP: Sparing the contralateral submandibular gland in oropharyngeal cancer patients: a planning study. Radiother Oncol. 2008, 89: 64-70. 10.1016/j.radonc.2008.04.008.
Saarilahti K, Kouri M, Collan J, Kangasmäki A, Atula T, Joensuu H, Tenhunen M: Sparing of the submandibular glands by intensity modulated radiotherapy in the treatment of head and neck cancer. Radiother Oncol. 2006, 78: 270-275. 10.1016/j.radonc.2006.02.017.
Wang Z-H, Yan C, Zhang Z-Y, Zhang CP, Hu HS, Tu WY, Kirwan J, Mendenhall WM: Impact of salivary gland dosimetry on post-IMRT recovery of saliva output and xerostomia grade for head-and-neck cancer patients treated with or without contralateral submandibular gland sparing: a longitudinal study. Int J Radiat Oncol Biol Phys. 2011, 81: 1479-1487. 10.1016/j.ijrobp.2010.07.1990.
RTOG 1216: randomized phase II/III trial of surgery and postoperative radiation delivered with concurrent cisplatin versus docetaxel versus docetaxel and cetuximab for high-risk squamous cell cancer of the head and neck. [http://www.rtog.org/ClinicalTrials/ProtocolTable/StudyDetails.aspx?study=1216]
National Cancer Institute: Common Terminology Criteria for Adverse Events Version 4.0. [http://evs.nci.nih.gov/ftp1/CTCAE/CTCAE_4.03_2010-06-14_QuickReference_5x7.pdf]
Fakhry C, Westra WH, Li S, Cmelak A, Ridge JA, Pinto H, Forastiere A, Gillison ML: Improved survival of patients with human papillomavirus-positive head and neck squamous cell carcinoma in a prospective clinical trial. J Natl Cancer Inst. 2008, 100: 261-269. 10.1093/jnci/djn011.
Collan J, Kapanen M, Mäkitie A, Nyman H, Joensuu H, Tenhunen M, Saarilahti K: Submandibular gland-sparing intensity modulated radiotherapy in the treatment of head and neck cancer: sites of locoregional relapse and survival. Acta Oncol. 2012, 51: 735-742. 10.3109/0284186X.2011.640348.
Cannon DM, Lee NY: Recurrence in region of spared parotid gland after definitive intensity-modulated radiotherapy for head and neck cancer. Int J Radiat Oncol Biol Phys. 2008, 70: 660-665. 10.1016/j.ijrobp.2007.09.018.
Eisbruch A, Marsh LH, Dawson LA, Bradford CR, Teknos TN, Chepeha DB, Worden FP, Urba S, Lin A, Schipper MJ, Wolf GT: Recurrences near base of skull after IMRT for head-and-neck cancer: implications for target delineation in high neck and for parotid gland sparing. Int J Radiat Oncol Biol Phys. 2004, 59: 28-42. 10.1016/j.ijrobp.2003.10.032.
Damast S, Wolden S, Lee N: Marginal recurrences after selective targeting with intensity-modulated radiotherapy for oral tongue cancer. Head Neck. 2012, 34: 900-906. 10.1002/hed.21677.
Chen AM, Farwell DG, Luu Q, Chen LM, Vijayakumar S, Purdy JA: Marginal misses after postoperative IMRT for head and neck cancer. Int J Radiat Oncol Biol Phys. 2011, 80: 1423-1429. 10.1016/j.ijrobp.2010.04.011.
Gregoire V, Levendag P, Ang KK, Bernier J, Braaksma M, Budach V, Chao C, Coche E, Cooper JS, Cosnard G, Eisbruch A, El-Sayed S, Emami B, Grau C, Hamoir M, Lee N, Maingon P, Muller K, Reychler H: CT-based delineation of lymph node levels and related CTVs in the node-negative neck: DAHANCA, EORTC, GORTEC, NCIC, RTOG consensus guidelines. Radiother Oncol. 2003, 69: 227-236. 10.1016/j.radonc.2003.09.011.
Doornaert P, Verbakel WF, Rietveld DH, Slotman BJ, Senan S: Sparing the contralateral submandibular gland without compromising PTV coverage by using volumetric modulated arc therapy. Radiat Oncol. 2011, 6: 74-10.1186/1748-717X-6-74.
Chajon E, Lafond C, Louvel G, Castelli J, Williaume D, Henry O, Jégoux F, Vauléon E, Manens JP, Le Prisé E, de Crevoisier R: Salivary gland-sparing other than parotid-sparing in definitive head-and-neck intensity-modulated radiotherapy does not seem to jeopardize local control. Radiat Oncol. 2013, 8: 132-10.1186/1748-717X-8-132.
We thank Dr. Ramesh Rengan for helpful discussions.
The authors declare that they have no competing interests.
MG participated in the design of the study, performed data collection and analysis, and drafted the manuscript along with UP. JL, AG, and GL contributed to the design of the study and revised the manuscript. UP participated in the design of the study and drafted the manuscript along with MG. All authors read and approved the final manuscript.