Chordomas and chondrosarcomas of the skull base: treatment and outcome analysis in a consecutive case series of 24 patients

World Journal of Surgical Oncology

Alessandro Paluzzi¹  Jameel Muzaffar¹  Paul Sanghera¹  Shahzada Ahmed¹  Christopher Metcalfe¹  Kevin Kulendra¹  Natarajan Saravanappa²  Simon Shaw²  Amjad Shad³ 

[1] Regional Skull-Base Unit, Queen Elizabeth Hospital, University Hospitals Birmingham, Mindelsohn Way, B15 2GW, Birmingham, UK;Royal Stoke University Hospital, Newcastle Road, ST4 6QG, Stoke-on-Trent, UK;University Hospital Coventry & Warwickshire, Clifford Bridge Road, CV2 2DX, Coventry, UK;

关键词: Chondrosarcoma;    Chordomas;    Skull base;    Endonasal;    Transnasal;    Proton beam therapy;   

DOI  :  10.1186/s12957-021-02178-6

来源: Springer

【 摘 要 】

BackgroundWe present our 9-year consecutive case series of skull base chordomas and chondrosarcomas from a UK tertiary referral centre, discussing treatments offered and outcomes. This was carried out to improve understanding around current treatment and to better inform the management of future patients.MethodsConsecutive case series over a 9-year period (2007–2016). Retrospective data analysis from the electronic skull base multidisciplinary team database and the digital patient records at a UK tertiary referral centreResultsTwenty-four patients were identified (11 chordomas, 13 chondrosarcomas, mean age 52). Nineteen had proton beam therapy (PBT) postoperatively; two had intensity-modulated radiotherapy; two had no further treatment. One patient was lost to follow-up. All chordomas were resected via a transnasal endoscopic approach. Of the 19 patients undergoing resection with PBT, 13 were disease free at latest follow-up, and six patients had local recurrence, of which two died (mean follow up 7.4 years). Of the three patients treated with surgery then IMRT/TomoTherapy, one died 4 years post-treatment, and the other two are alive after 4 and 5 years of follow-up respectively. Of the two patients treated with surgery alone, one was lost to follow-up, and the other is alive after more than 8 years. Chondrosarcoma 5-year survival was 91.6%, and chordoma 4-year survival was 75%.ConclusionSkull base chordomas and chondrosarcomas can be challenging to resect, and most cases require adjuvant therapy to achieve control. Where complete resection is not possible, it is critical to undertake sufficient resection to permit high-dose radiation.

【 授权许可】

CC BY