Outcomes After Definitive Surgery for Spinal and Sacral Chordoma in 101 Patients Over 20 Years

Author:

Xia Yuanxuan1ORCID,Papali Pritika1,Al-Mistarehi Abdel-Hameed1,Hansen Landon J.1,Azad Tej D.1,Ahmed A. Karim1,Meyer Christian2,Gross John3,Khan Majid4,Bettegowda Chetan1,Mukherjee Debraj1,Witham Timothy1,Bydon Ali1,Theodore Nicholas1,Wolinsky Jean-Paul5,Gokaslan Ziya6,Larry Lo Sheng-Fu7,Sciubba Daniel7,Lee Sang H.8,Redmond Kristin J.9,Lubelski Daniel1

Affiliation:

1. Department of Neurosurgery, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA;

2. Division of Medical Oncology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA;

3. Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA;

4. Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA;

5. Department of Neurosurgery, Northwestern University, Chicago, Illinois, USA;

6. Department of Neurosurgery, The Warren Alpert Medical School of Brown University, Providence, Rhode Island, USA;

7. Department of Neurosurgery, Zucker School of Medicine at Hofstra, Manhasset, New York, USA;

8. Department of Orthopedic Surgery, The Johns Hopkins Hospital, Baltimore, Maryland, USA;

9. Department of Radiation Oncology and Molecular Radiation Sciences, The Johns Hopkins Hospital, Baltimore, Maryland, USA

Abstract

BACKGROUND AND OBJECTIVES: Spinal chordomas are primary bone tumors where surgery remains the primary treatment. However, their low incidence, lack of evidence, and late disease presentation make them challenging to manage. Here, we report the postoperative outcomes of a large cohort of patients after surgical resection, investigate predictors for overall survival (OS) and local recurrence-free survival (LRFS) times, and trend functional outcomes over multiple time periods. METHODS: Retrospective review of all patients followed for spinal chordoma at a quaternary spinal oncology center from 2003 to 2023 was included. Data were collected regarding demographics, preoperative and perioperative management, and follow-up since initial definitive surgery. Primary outcomes were OS and LRFS, whereas secondary outcomes were functional deficits. RESULTS: One hundred one patients had an average follow-up of 6.0 ± 4.2 years. At the time of census, 25/101 (24.8%) had experienced a recurrence and 10/101 (9.9%) had died. After surgery, patients experienced a significant decrease in pain over time, but rates of sensory deficits, weakness, and bowel/bladder dysfunction remained static. Tumors ≥100 cm3 (hazard ratio (HR) = 5.89, 95% CI 1.72-20.18, P = .005) and mobile spine chordomas (HR = 7.73, 95% CI 2.09-28.59, P = .002) are related to worse LRFS, whereas having neoadjuvant radiotherapy is associated with improved LRFS (HR = 0.09, 95% CI 0.01-0.88, P = .038). On the other hand, being age ≥65 years was associated with decreased OS (HR = 16.70, 95% CI 1.54-181.28, P = .021). CONCLUSION: Surgeons must often weigh the pros and cons of en bloc resection and sacrificing important but affected native tissues. Our findings can provide a benchmark for counseling patients with spinal chordoma. Tumors ≥100 cm3 appear to have a 5.89-times higher risk of recurrence, mobile spine chordomas have a 7.73 times higher risk, and neoadjuvant radiotherapy confers an 11.1 times lower risk for local recurrence. Patients age ≥65 years at surgery have a 16.70 times higher risk of mortality than those <65 years.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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