High-dose proton beam therapy for sinonasal mucosal malignant melanoma
© Fuji et al.; licensee BioMed Central Ltd. 2014
Received: 18 December 2013
Accepted: 12 July 2014
Published: 23 July 2014
The significance of definitive radiotherapy for sinonasal mucosal melanoma (SMM) is sill controvertial. T his study was to evaluate the role of high-dose proton beam therapy (PBT) in patients with SMM.
The cases of 20 patients with SMM localized to the primary site who were treated by PBT between 2006 and 2012 were retrospectively analyzed. The patterns of overall survival and morbidity were assessed.
The median follow-up time was 35 months (range, 6–77 months). The 5-year overall and disease-free survival rates were 51% and 38%, respectively. Four patients showed local failure, 2 showed regrowth of the primary tumor, and 2 showed new sinonasal tumors beyond the primary site. The 5-year local control rate after PBT was 62%. Nodal and distant failure was seen in 7 patients. Three grade 4 late toxicities were observed in tumor-involved optic nerve.
Our findings suggested that high-dose PBT is an effective local treatment that is less invasive than surgery but with comparable outcomes.
Sinonasal mucosal melanoma (SMM) is a rare disease accounting for 0.3–2% of all malignant melanomas in North America . Its prognosis is much worse than that of cutaneous malignant melanoma; the overall 5-year survival rate of patients with SMM is reported to be 34%  whereas that of patients with head and neck cutaneous melanoma is reported to be 80% . Surgery has been the main option for eradicating the disease [4–6]. However, in a review of cases from a high-volume cancer center in North America, recurrence of the primary disease was observed in 50% of cases [7–9].
For patients with SMM, radiotherapy has been employed for palliation or as adjuvant treatment for surgery. However, a nationwide survey recently performed in the United States revealed that radiotherapy has a limited role in improving overall patient survival . Definitive radiotherapy for SMM has been applied selectively because of tumor radioresistance and the propensity for metastases to distant organs. Furthermore, in the case of SMM, intensive radiotherapy is only applicable to a small proportion of patients because the tumors are frequently surrounded by radiosensitive critical tissues, e.g., the optic nerve, cranial nerves, and the brain stem.
Highly conformal beam delivery techniques are promising measures with which to deliver definitive high-dose radiotherapy in patients with SMM. Intensity-modulated radiotherapy and particle beam therapy have both been reported to facilitate the delivery of high doses to the residual tumor while minimizing exposure to the surrounding normal tissues [10–14].
In a short-term analysis, the primary disease control rate associated with high-dose conformal proton beam therapy was reported to be promising . These data propose a definitive role for proton beam therapy; however, the actual efficacy of this treatment with escalating prescribed dose needs to be established for long-term tumor control and the morbidity in critical organs at the irradiated sites needs to be evaluated. Furthermore, the significance of the local treatment for improved overall survival and the pattern of relapse needs to be analyzed with a sufficient follow-up time. The purpose of this study therefore was to describe the long-term course of patients undergoing definitive high-dose PBT for localized SMM.
Patients and methods
Median age (years, range)
Tumor size (mm, range)
Small cell type
Spindle cell type
The median time interval between diagnosis and the start of PBT was 4.8 months (range, 0.5–56.2 months). Nine patients had recurrent disease after local surgery before being referred to our institute. Seven patients underwent 1–8 cycles of systemic chemotherapy before PBT. All patients underwent definitive PBT because gross tumor volume was observed at the start of PBT. Sixteen patients underwent concurrent or adjuvant multi-agent chemotherapy consisting of dacarbazine, nimustine, and vincristine or dacarbazine, nimustine, cisplatin, and tamoxifen. The treatment period of concurrent or adjuvant chemotherapy was 8 months (4–12 months).
Proton beam therapy
The gross tumor volume (GTV) was defined as the gross extent of the tumor as observed on CT or MRI images. Areas showing elevated FDG-PET signals were also included in the GTV. The clinical target volume (CTV) was defined as GTV with a 2–10 mm margin. Areas with mucosal alteration and inflammatory tissue as seen on a T2-weighted image were also included in the CTV. The planning target volume (PTV) was defined by adding a 3-mm margin to the GTV and CTV, referred to as the PTV(GTV) and PTV(CTV), respectively.
A proton beam has a unique depth-dose curve, the so-called Bragg peak and deposits a maximum energy at a designated depth. With this physical feature, the proton beam provides highly conformal dose deposition for SMM. The proton beam used in this study was 150 MV, passive scattering beam. The biological effectiveness of proton on using PBT differs from that of photons on using conventional radiation because of this unique mechanism of energy deposition. On considering the relative biological effect of a proton beam, the dose was reported in grays relative biological effectiveness, Gy (RBE), which was equivalent to the physical dose in Gy multiplied by 1.1. A hypofractionated treatment schedule of 3.5 Gy (RBE) per fraction administered daily for a total dose of 70 Gy (RBE) in 20 fractions was applied.
Overall survival, disease-free survival, and local control rates were estimated using the Kaplan–Meier method. All events were calculated from the first day of PBT to the last day of follow-up. Local failure comprised both progression of the primary tumor and appearance of a new lesion at the sinonasal site after PBT. Standard errors for estimated survival were compared using a log-rank test for association among potential prognostic factors. A p value of ≤0.05 was considered statistically significant. All statistical analyses were performed using PASW 17.0 (PASW, Chicago, Illinois).
Tumor recurrence and survival
Distant metastases were observed 7 patients (liver, 3; lung, 2; brain, 1; and intestine, 1). Three patients showed lymph node involvement after PBT.Differentiated morphology presenting as epithelioid and spindle cell type cells was associated with significantly better overall survival (p = 0.018) (Figure 2D). Other candidate prognostic factors including T stage, use of concurrent chemotherapy, FDG-PET signal level, and tumor size did not show any significant association with survival.
Acute toxicities of proton beam therapy
Eyelid function disorder
Late toxicities of proton beam therapy
Optic nerve disorder
Middle ear inflammation
Five patients presented with osteonecrosis in irradiated field. Initially, those patients suffered with the pain of affected bone. However, a course of antibiotics relieved the pain and enable to take food. Radiation-induced grade 2 otitis was observed in 7 patients; this could be controlled with antibiotic administration in all cases. Watering eyes due to lacrimal duct obstruction were most frequent late adverse events.
In this study, high-dose PBT resulted in favorable primary disease control. Most reviews on the management of head and neck mucosal melanoma suggest that radiotherapy has only a minor role and is mostly used as adjuvant treatment. However, it has been suggested that these treatments could provide an option for eradication of primary disease. A study of 85 carbon ion-treated cases reported a 5-year actuarial local control rate of 75% [12, 13]. Short-term analysis of PBT also showed promising outcomes with a 3-year local control rate of 86% .
The current study showed that the primary disease was controlled in all patients within 3 years. The higher primary disease control rate most likely contributed to the improved overall survival of the cohort. The 5-year overall survival rate achieved here is comparable with those reported for surgery [2, 8].
There are two cases developed recurrent disease outside of primary gross disease. Although in-transit spreading is known to be a major feature of mucosal melanoma, we have few knowledge for detecting microscopical infiltration of mucosal melanoma. Recent advantage of high sensitive imaging technology, like FDG-PET and other more specific imaging technique or both could be useful tool for defining irradiation target volume of mucosal melanoma. However, defining the border of tumor abutted brain or occulomotor is still challenging, because the both show higher uptake of FDG. Another type of radiotracer specific for melanin in melanoma cells, known as a benzamide derivative could be useful for defining the extension of tumor arose head and neck region .
Comparison between treatment outcomes of carbon ion beam and those of proton beam do not suggest apparent superiority of carbon ion treatment. Reported local control rate 3 years after carbon ion treatment ranged from 65% to 85% [12, 13]. Current study showed that local control rate of 87% at 3 years after treatment. Better local control rate, 75% at 5 years after carbon ion treatment has been reported . However, more censored cases with lower long term survival rate of the study remains the uncertainties of long term local disease control rate. Short term analysis of carbon ion beam and proton beam implemented for head and neck melanoma at same institute showed identical local control rate at 2 years after treatment .
Here, the analyses involved dose escalation and hypofractionated schemes as well as other definitive therapies with other particle beam therapy series. The prescribed doses of those particle beam treatments can be converted to 84–91 Gy in equivalent dose in 2 Gy fractions.(EQD2) of a standard fractionation scheme. These are 1.2–1.5 times higher than those employed for other head and neck tumors. Nevertheless, 2 cases of primary tumor relapse were observed 4 years after PBT. Delayed recurrence of irradiated tumors needs to be recognized as a possible characteristic of high-dose radiotherapy.
Reported intensive radiotherapy for mucosal melanoma is usually scheduled for 1–4 days/week [10–14, 16]. In contrast, the current treatment plan involved a conventional schedule of 5 days/week. In terms of the deposited dose at the target, the 3.5-Gy (RBE) fraction size used here is regarded as hypofractionated but has been reported to be effective for eradicating mucosal melanoma. However, a treatment planning technique known as simultaneous integrated boost (SIB) facilitates a decreased dose per each fraction (i.e., 2 Gy (RBE) per fraction) for critical structures in the CTV. The use of the SIB technique here, even in a hypofractionated schedule, enabled the application of a constraint dose and an estimation of toxicity based on the knowledge of standard daily fractionated treatment.
We encountered 2 cases of optic nerve impairment after ablative dose delivery to the nerve. For these patients, the intention of treatment was both eradication of the tumor and preservation of contralateral visual function. Therefore, differentiated doses were employed for optic nerves. The affected optic nerve received 64 Gy, whereas the contralateral site received <50 Gy. Thus, the primary disease was controlled for 4-years and contralateral vision was preserved, suggesting that this treatment is an acceptable option for patients with unilateral optic nerve involvement or those offered optic nerve transection.
The establishment of prognostic factors to identify patients who would benefit from PBT is essential. In the current study, differentiated cellular morphology was a significant survival factor, However, an obvious limitation of the current study is the small sample size. A future analysis of a large cohort of patients treated with PBT would help reinforce the significance of cellular morphology as a prognostic indicator.
We did not implemented prophylactic cervical lymph node irradiation because the prophylactic treatment plays a limited role for improvement of survival. Gilligan reported 8 cases developed lymph node recurrence among 28 patients who underwent definitive radiotherapy for sinonasal melanoma . Of eight patients, six patients emerged with concomitant disease of primary tumor recurrence or distant metastasis. In current study, we observed three cases developed neck lymph node metastasis among 20 cohort. Of three, two patients presented with recurrence at primary site or other organs. One patient without other recurrent disease was salvaged with neck dissection.
In the present study, chemotherapy was administered to 16 of 20 patients, which likely played a substantial therapeutic role because a gradual decrease in tumor markers was noted during treatment. Considering the diverse backgrounds of patients with respect to treatment modalities, the current analysis was not appropriate for evaluating chemotherapeutic benefits. Chemotherapy-induced cytotoxicity during and after the PBT is a concern; however, no patients receiving chemotherapy suffered from unexpected treatment interruptions and only 1 case of grade 4 hematological toxicity was encountered. Therefore, concurrent chemotherapy was feasible, but its significance for tumor control remains to be determined.
Hypofractionated high-dose PBT reported here improved the local control rate associated with SMM. The sustained control of the primary lesion resulted in a favorable survival rate, comparable to that achieved by surgery in patients with certain tumor types.
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