Abstract

PurposeWe report our experience of intensity‐modulated proton and carbon‐ion radiotherapy (IMPT/IMCT) for head and neck sarcomas (HNS).Methods and MaterialsAn analysis of the ongoing prospective data registry from the Shanghai Proton and Heavy Ion Center (SPHIC) for patients with HNS was conducted. The 12‐ and 24‐month rates of local recurrence‐free, overall, distant metastasis‐free, progression‐free survival (LRFS, OS, DMFS, and PFS), and acute/late toxicities were calculated. The prognostic factors for the effectiveness of the treatment were also analyzed.ResultsBetween 7/2014 and 5/2018, 51 consecutive patients with HNS received definitive doses of IMCT (41 cases), IMPT (two cases), or their combination (eight cases). One patient had R0 resection and another treated on the Chinese Food and Drug Administration registration trial received IMPT only. Twenty‐seven patients were treated according to various dose escalation trials or institutional protocols using IMCT or IMPT + IMCT boost. Twenty‐two patients with locoregional recurrence (10 and four patients failed surgery or surgery followed by radiotherapy, respectively) or radiation‐induced second primary sarcomas (eight patients) received salvage particle radiotherapy. With a median follow‐up time of 15.7 months, four patients with second primary sarcoma died. The 1‐ and 2‐year OS, PFS, LRFS, and DMFS rates for the entire cohort were 92.9% vs 90%, 73.6% vs 57.4%, 88.4% vs 78.9%, and 84.6% vs 76.5%, respectively. Those rates for patients without prior radiotherapy were 100% vs 100%, 82.1% vs 65.8%, 93.6% vs 85.3%, and 88.4% vs 79.5%, respectively. Multivariate analyses revealed that re‐irradiation was an independent prognostic factor for both LRFS and PFS (P = 0.015 and 0.037, respectively). In addition, gross tumor volume (GTV) was an independent prognostic factor for PFS (P = 0.048). One patient experienced Grade 3 acute toxicity (oral mucositis); another experienced Grade 4 acute event (hemorrhage) which required embolization. He lately died from hemorrhage (Grade 5) at 3.4 months after the completion of treatment. No patient experienced radiation‐induced acute/late toxicity of ≥ Grade 2 otherwise.ConclusionWith few observed acute/late toxicities, IMPT/IMCT provided effective short‐term tumor control in our patients with HNS. Further investigations, preferably in a prospective fashion, will be required to confirm the efficacy and toxicities of IMPT/IMCT in this group of patients.

Highlights

  • Head and neck sarcomas (HNS) arise from mesenchymal tissues and represent a rare and heterogeneous disease entity

  • Sarcomas account for 1% of all head and neck malignancies, and ~ 10% of all sarcomas occur within the head and neck.[1,2,3,4,5]

  • Even with aggressive local therapy, the prognosis of HNS is worse than sarcomas that originate in other anatomical locations.[8,9]

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Summary

Introduction

Head and neck sarcomas (HNS) arise from mesenchymal tissues and represent a rare and heterogeneous disease entity. Even with aggressive local therapy, the prognosis of HNS is worse than sarcomas that originate in other anatomical locations.[8,9] When complete resection is not feasible, photon‐ based RT rarely provides adequate long‐term local control, as most sarcoma subtypes are inherently resistant to conventional RT.[10,11,12,13,14] This reduces the likelihood of long‐term survival.[11] Dose escalation for photon‐based RT is usually not feasible, due to the dose limitation of the adjacent critical organs at risk (OARs). Patients who develop recurrences from previously irradiated HNS or de novo sarcomas secondary to previous RT for an unrelated malignancy carry a dismal prognosis, given the accumulated doses received by the OARs and emergence of radioresistant tumors

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