Treatment of intramedullary spinal cord tumors: a modified Delphi technique of the North American Spine Society Section of Spine Oncology

Author:

Hersh Andrew M.1,Pennington Zach2,Lubelski Daniel1,Elsamadicy Aladine A.3,Dea Nicolas4,Desai Atman5,Gokaslan Ziya L.6,Goodwin C. Rory7,Hsu Wesley8,Jallo George I.9,Krishnaney Ajit10,Laufer Ilya11,Lo Sheng-Fu Larry12,Macki Mohamed13,Mehta Ankit I.14,Ozturk Ali15,Shin John H.16,Soliman Hesham12,Sciubba Daniel M.112

Affiliation:

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

2. Department of Neurosurgery, Mayo Clinic, Rochester, Minnesota;

3. Department of Neurosurgery, Yale School of Medicine, New Haven, Connecticut;

4. Department of Neurosurgery, Vancouver Spine Surgery Institute, University of British Columbia, Vancouver, British Columbia, Canada;

5. Department of Neurosurgery, Stanford Medicine, Palo Alto, California;

6. Department of Neurosurgery, Brown University, Providence, Rhode Island;

7. Department of Neurosurgery, Duke University Medical Center, Durham, North Carolina;

8. Department of Neurological Surgery, Wake Forest University School of Medicine, Winston-Salem, North Carolina;

9. Department of Neurosurgery, Johns Hopkins Medicine, Institute for Brain Protection Sciences, Johns Hopkins All Children’s Hospital, St. Petersburg, Florida;

10. Department of Neurosurgery, Cleveland Clinic, Cleveland, Ohio;

11. Department of Neurosurgery, New York University Grossman School of Medicine, New York, New York;

12. Department of Neurosurgery, Donald and Barbara Zucker School of Medicine at Hofstra, Long Island Jewish Medical Center and North Shore University Hospital, Northwell Health, Manhasset, New York;

13. Department of Neurosurgery, University of California San Francisco School of Medicine, San Francisco, California;

14. Department of Neurosurgery, University of Illinois at Chicago, Illinois;

15. Department of Neurosurgery, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania; and

16. Department of Neurosurgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts

Abstract

OBJECTIVE Intramedullary spinal cord tumors (IMSCTs) are rare tumors with heterogeneous presentations and natural histories that complicate their management. Standardized guidelines are lacking on when to surgically intervene and the appropriate aggressiveness of resection, especially given the risk of new neurological deficits following resection of infiltrative tumors. Here, the authors present the results of a modified Delphi method using input from surgeons experienced with IMSCT removal to construct a framework for the operative management of IMSCTs based on the clinical, radiographic, and tumor-specific characteristics. METHODS A modified Delphi technique was conducted using a group of 14 neurosurgeons experienced in IMSCT resection. Three rounds of written correspondence, surveys, and videoconferencing were carried out. Participants were queried about clinical and radiographic criteria used to determine operative candidacy and guide decision-making. Members then completed a final survey indicating their choice of observation or surgery, choice of resection strategy, and decision to perform duraplasty, in response to a set of patient- and tumor-specific characteristics. Consensus was defined as ≥ 80% agreement, while responses with 70%–79% agreement were defined as agreement. RESULTS Thirty-six total characteristics were assessed. There was consensus favoring surgical intervention for patients with new-onset myelopathy (86% agreement), chronic myelopathy (86%), or progression from mild to disabling numbness (86%), but disagreement for patients with mild numbness or chronic paraplegia. Age was not a determinant of operative candidacy except among frail patients, who were deemed more suitable for observation (93%). Well-circumscribed (93%) or posteriorly located tumors reaching the surface (86%) were consensus surgical lesions, and participants agreed that the presence of syringomyelia (71%) and peritumoral T2 signal change (79%) were favorable indications for surgery. There was consensus that complete loss of transcranial motor evoked potentials with a 50% decrease in the D-wave amplitude should halt further resection (93%). Preoperative symptoms seldom influenced choice of resection strategy, while a distinct cleavage plane (100%) or visible tumor-cord margins (100%) strongly favored gross-total resection. CONCLUSIONS The authors present a modified Delphi technique highlighting areas of consensus and agreement regarding surgical management of IMSCTs. Although not intended as a substitute for individual clinical decision-making, the results can help guide care of these patients. Additionally, areas of controversy meriting further investigation are highlighted.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

Reference52 articles.

1. Predictors of survival and time to progression following operative management of intramedullary spinal cord astrocytomas;Hersh AM,2022

2. Perioperative outcomes and survival after surgery for intramedullary spinal cord tumors: a single-institutional series of 302 patients;Hersh AM,2022

3. Intramedullary spinal cord tumors: a review of current and future treatment strategies;Tobin MK,2015

4. Intramedullary spinal cord tumors: part i-epidemiology, pathophysiology, and diagnosis;Samartzis D,2015

5. Surgical approaches to intramedullary spinal cord astrocytomas in the age of genomics;Hersh AM,2022

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