Pre-operative Radiotherapy for Sinonasal Squamous Cell Carcinoma: outcomes and patient selection

Poster abstract

Purpose/Objective

Resectable sinonasal squamous cell carcinoma (SNSCC) is often managed by surgery +/- post-operative radiation (postop-RT), guided by surgical pathology. In our institution, pre-operative radiation (preop-RT) +/- chemotherapy has been used in select cases after multidisciplinary input from radiation, surgical, and medical oncology teams. Preop-RT has the advantages of lower dose and smaller/better defined volumes in non-surgically perturbed tissues, which can be especially important for treatment approximating optic structures. The aim of this study is to evaluate preop-RT, compared to standard postop-RT, in patients with SNSCC, focusing on oncologic outcomes and patient selection.

Material/Methods

All newly diagnosed SNSCC treated with preop-RT or postop-RT from 2005 to 2021 were included. Clinical characteristics and outcomes were compared between preop-RT vs postop-RT cohorts. Outcome endpoints included overall survival (OS), disease-free survival (DFS), locoregional control (LRC) and distant control (DC). OS and DFS were estimated with Kaplan-Meier method while LRC and DC were calculated with competing risk methods.

Results

A total of 72 patients were eligible: 25 received preop-RT and 47 postop-RT. The preop-RT cohort comprised more origin from the ethmoid sinus (44% vs 0%, p<0.001), and more T3-T4 diseases (versus T1-2) at presentation (96% vs 68%, p<0.01). HPV testing was not performed in the majority of cases; among those tested, two out of 8 (25%) SNSCC tested p16-positive in the preop-RT cohort and 13 out of 18 (72%) in the postop-RT cohort. The remaining baseline characteristics were similar between the preop-RT vs postop-RT cohorts. The documented clinical reasons for pre-operative radiation included minimizing dose to preserve orbital structures and avoidance of orbital exenteration (n=12, 48%), improving resection margin clearance (n=7, 28%), and reducing extent and morbidity of the surgical approach (n=4, 16%). All patients in preop-RT cohort received 50 Gy in 25 fractions (50 Gy/25f) to the primary site, with 7 patients receiving a boost to 60 Gy (6 patients with simultaneous integrated boost, 1 patient with sequential 10 Gy/5f boost). The reasons for boost were treatment of gross/equivocal nodal disease to spare a neck dissection (n=4, 57%), or high-risk surgical regions with a high likelihood of a R1 resection based on a pre-emptive discussion with the surgical team (n=3, 43%). Three patients received concurrent cisplatin chemotherapy. Patients in the postop-RT cohort received 60 Gy/30f (n=11), 66 Gy/33f (n=20), 70 Gy/33-35f (n=11), and other (n=5). Fourteen (56%) preop-RT patients had complete pathological responses. The median follow-up was 5.5 and 5.2 years for the preop-RT and postop-RT cohort, respectively. Oncologic outcomes at 5-years were similar between preop-RT and postop-RT cohorts: OS 76% vs 69% (p=0.799), DFS 66% vs 62% (p=0.892), LRC 78% vs 69% (p=0.313), and DC 92% vs 88% (p=0.919), respectively (Table 1).  

Table 1. Oncologic Outcomes

 

Postop-RT (n=47)

Preop-RT (n=25)

P value

5-year Outcomes

 

 

 

OS

69% (57-85)

76% (61-95)

0.799

DFS

62% (50-78)

66% (49-89)

0.892

LRC

69% (52-80)

78% (50-90)

0.313

DC

88% (72-95)

92% (69-98)

0.919

Conclusion

With multidisciplinary decision-making for SNSCC, preop-RT is correlated with pathologic complete response, and lower doses to critical normal tissues. Oncologic outcomes are comparable between the two groups despite more T3-T4 disease in the preop-RT cohort. In the setting of collaborative multidisciplinary care in a high-volume centre, pre-op RT in the management of locally advanced resectable sinonasal SCC is a reasonable, and possibly preferred, option in select patients to minimize dose to optic structures and improve margin clearance.

Authors
1Revadhi Chelvarajah, 1Shao Hui Huang, 2Jie Su, 1Jolie Ringash, 3Ian Witterick, 3John de Almeida, 3Eric Monteiro, 4Anna Spreafico, 1John Waldron, 1Brian O'Sullivan, 1Ali Hosni Abdalaty, 1Scott Bratman, 1B.C. John Cho, 1Andrew Hope, 1John Kim, 1Andrew McPartlin, 1C. Jillian Tsai, 1Li Tong, 2Wei Xu, 1Ezra Hahn
1Princess Margaret Cancer Centre, Radiation Oncology, Toronto, Canada. 2Princess Margaret Cancer Centre, Biostatistics, Toronto, Canada. 3Mount Sinai Hospital, Head and Neck Surgical Oncology, Toronto, Canada. 4Princess Margaret Cancer Centre, Division of Medical Oncology, Toronto, Canada