| Literature DB >> 31179239 |
Wojciech Golusiński1, Ewelina Golusińska-Kardach1.
Abstract
In the last few decades, the surgical treatment of oropharyngeal squamous cell carcinoma (OPSCC) has undergone enormous changes. Until the 1990s, open surgery was the primary treatment for OPSCC. However, due to the potentially severe functional morbidity of this approach, open surgery was largely displaced by concurrent chemoradiotherapy (CRT) in the 1990s. At the same time, new, less-invasive surgical approaches such as transoral surgery with monopolar cautery began to emerge, with the potential to reduce functional morbidity and avoid the late-onset toxicity of CRT. More recently, the growing incidence of HPV-positive disease has altered the patient profile of OPSCC, as these patients tend to be younger and have a better long-term prognosis. Consequently, this has further bolstered interest in minimally-invasive techniques to de-intensify treatment to reduce long-term toxicity and treatment-related morbidity. In this context, there has been a renewed interest in the primary surgery, which allows for accurate pathologic staging and thus-potentially-de-intensification of postoperative CRT. The continuous advances in minimally-invasive surgical approaches, including transoral laser microsurgery (TLM) and transoral robotic surgery (TORS), have also altered the surgical landscape. These minimally-invasive approaches offer excellent functional outcomes, without the severe toxicity associated with intensive CRT, thus substantially reducing treatment-related morbidity. In short, given the increasing prevalence of HPV-positive OPSCC, together with the severe long-term sequela of aggressive CRT, surgery appears to be recapturing its previous role as the primary treatment modality for this disease. While a growing body of evidence suggests that TLM and TORS offer oncologic outcomes that are comparable to CRT and open surgery, many questions remain due to the lack of prospective data. In the present review, we explore the emerging range of surgical options and discuss future directions in the treatment of OPSCC, including the most relevant clinical trials currently underway.Entities:
Keywords: TLM; TORS; cancer; oropharynx; surgery
Year: 2019 PMID: 31179239 PMCID: PMC6542993 DOI: 10.3389/fonc.2019.00388
Source DB: PubMed Journal: Front Oncol ISSN: 2234-943X Impact factor: 6.244
Figure 1Scheme of treatment of oropharyngeal cancer.
Oncological outcomes of TORS for oropharyngeal squamous cell carcinoma.
| Weinstein ( | 2012 | Prospective | TORS | Tonsil | T1-T4 | 30 | 2.7 years | 97% | 97% | OS = 100% |
| de Almeida ( | 2015 | Retrospective, multicentre | TORS | Oropharynx | Tx–T4 | 364 | 20 months | 95.6% (3 year) | 3-years: 88.8% | OS (3 year) = 87.1% |
| Kass ( | 2016 | Retrospective | TORS = 42% | Oropharynx | T1-T2 | 143 | 41 months | NR | NR | RFS (3 year) = 87% (TORS) |
| Dabas ( | 2017 | Prospective | TORS | BOT | T1-T2 | 57 | 29 months | NR | 95.8% | DFS = 89.6% |
| Moore ( | 2017 | Retrospective | TORS | Tonsil | Tx-T4 | 314 | 3.3 years | NR | 92% (5 years) | OS = 86% |
| Min ( | 2017 | Prospective | TORS | Pyriform | T1-T4 | 38 | 60 months | 97.4% | NR | OS = 55.3% |
| Doazan ( | 2018 | Retrospective, multicentre | TORS | Supraglottic | T1-T3 | 122 | 42.8 months | 2 year: 94.3% 5 year: 90.2% | 2 year: 91.8% | 2/5 year OS = 86.9%/78.7% |
| Baliga ( | 2018 | Retrospective (cancer registry) | TORS | Oropharynx | T1-T2 | 2680 | 31.4 months | NR | NR | 5 year OS = 84% |
NR, not reported; TORS, transoral robotic surgery; DFS, disease-free survival; RFS, relapse-free survival; OS, overall survival; BOT, base of tongue.
Contraindications for TORS.
| •Tonsillar involvement with a retropharyngeal carotid artery |
| •Tumor located at the midline of the tongue base or vallecula |
| •Tumor located adjacent to the carotid bulb or internal carotid artery |
| •Carotid artery enveloped by tumor or metastatic lymph nodes |
| •Tumor resection requiring ≥50% of the deep tongue base musculature or posterior pharyngeal wall |
| •Resection of the tongue base and entire epiglottis |
| •Stage T4b |
| •Unresectable neck disease |
| •Multiple distant metastases |
| •Neoplastic-related trismus |
| •Prevertebral fascia involvement |
| •Mandible or hyoid involvement |
| •Tumor extension to lateral neck soft tissues |
| •Involvement of the eustachian tube |