Magnetic resonance–guided stereotactic laser ablation therapy for the treatment of pediatric brain tumors: a multiinstitutional retrospective study

Author:

Arocho-Quinones Elsa V.1,Lew Sean M.12,Handler Michael H.3,Tovar-Spinoza Zulma4,Smyth Matthew5,Bollo Robert6,Donahue David7,Perry M. Scott8,Levy Michael L.9,Gonda David9,Mangano Francesco T.10,Storm Phillip B.11,Price Angela V.12,Couture Daniel E.13,Oluigbo Chima14,Duhaime Ann-Christine15,Barnett Gene H.16,Muh Carrie R.17,Sather Michael D.18,Fallah Aria19,Wang Anthony C.19,Bhatia Sanjiv20,Patel Kadam21,Tarima Sergey21,Graber Sarah3,Huckins Sean4,Hafez Daniel M.5,Rumalla Kavelin5,Bailey Laurie7,Shandley Sabrina7,Roach Ashton10,Alexander Erin11,Jenkins Wendy13,Tsering Deki14,Price George15,Meola Antonio16,Evanoff Wendi16,Thompson Eric M.17,Brandmeir Nicholas18,the Pediatric Stereotactic Laser Ab

Affiliation:

1. Department of Neurosurgery, Medical College of Wisconsin, Milwaukee, Wisconsin;

2. Department of Neurosurgery, Children’s Hospital of Wisconsin, Milwaukee, Wisconsin;

3. Department of Neurosurgery, Children’s Hospital Colorado, Aurora, Colorado;

4. Department of Neurosurgery, SUNY Upstate Medical University, Syracuse, New York;

5. Department of Neurosurgery, St. Louis Children’s Hospital, St. Louis, Missouri;

6. Department of Neurosurgery, Primary Children’s Hospital, Salt Lake City, Utah;

7. Departments of Neurosurgery and

8. Neurology, Cook Children’s Hospital, Fort Worth, Texas;

9. Department of Neurosurgery, Rady Children’s Hospital-San Diego, California;

10. Department of Neurosurgery, Cincinnati Children’s Hospital, Cincinnati, Ohio;

11. Department of Neurosurgery, Children’s Hospital of Philadelphia, Pennsylvania;

12. Department of Neurosurgery, University of Texas Southwestern Medical Center, Dallas, Texas;

13. Department of Neurosurgery, Wake Forest Baptist Health, Winston-Salem, North Carolina;

14. Department of Neurosurgery, Children’s National Health System, Washington, DC;

15. Department of Neurosurgery, Massachusetts General Hospital for Children, Boston, Massachusetts;

16. Department of Neurosurgery, Cleveland Clinic Children’s, Cleveland, Ohio;

17. Department of Neurosurgery, Duke Children’s Hospital, Durham, North Carolina;

18. Department of Neurosurgery, Penn State Health, Hershey, Pennsylvania;

19. Department of Neurosurgery, UCLA Mattel Children’s Hospital, Los Angeles, California;

20. Department of Neurosurgery, Nicklaus Children’s Hospital, Miami, Florida; and

21. Department of Biostatistics, Medical College of Wisconsin, Milwaukee, Wisconsin

Abstract

OBJECTIVEThis study aimed to assess the safety and efficacy of MR-guided stereotactic laser ablation (SLA) therapy in the treatment of pediatric brain tumors.METHODSData from 17 North American centers were retrospectively reviewed. Clinical, technical, and radiographic data for pediatric patients treated with SLA for a diagnosis of brain tumor from 2008 to 2016 were collected and analyzed.RESULTSA total of 86 patients (mean age 12.2 ± 4.5 years) with 76 low-grade (I or II) and 10 high-grade (III or IV) tumors were included. Tumor location included lobar (38.4%), deep (45.3%), and cerebellar (16.3%) compartments. The mean follow-up time was 24 months (median 18 months, range 3–72 months). At the last follow-up, the volume of SLA-treated tumors had decreased in 80.6% of patients with follow-up data. Patients with high-grade tumors were more likely to have an unchanged or larger tumor size after SLA treatment than those with low-grade tumors (OR 7.49, p = 0.0364). Subsequent surgery and adjuvant treatment were not required after SLA treatment in 90.4% and 86.7% of patients, respectively. Patients with high-grade tumors were more likely to receive subsequent surgery (OR 2.25, p = 0.4957) and adjuvant treatment (OR 3.77, p = 0.1711) after SLA therapy, without reaching significance. A total of 29 acute complications in 23 patients were reported and included malpositioned catheters (n = 3), intracranial hemorrhages (n = 2), transient neurological deficits (n = 11), permanent neurological deficits (n = 5), symptomatic perilesional edema (n = 2), hydrocephalus (n = 4), and death (n = 2). On long-term follow-up, 3 patients were reported to have worsened neuropsychological test results. Pre-SLA tumor volume, tumor location, number of laser trajectories, and number of lesions created did not result in a significantly increased risk of complications; however, the odds of complications increased by 14% (OR 1.14, p = 0.0159) with every 1-cm3 increase in the volume of the lesion created.CONCLUSIONSSLA is an effective, minimally invasive treatment option for pediatric brain tumors, although it is not without risks. Limiting the volume of the generated thermal lesion may help decrease the incidence of complications.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

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2. stereotactic laser ablation as treatment of brain metastases recurring after stereotactic radiosurgery: a systematic literature review;Alattar;World Neurosurg,2019

3. Volumetric response of progressing post-SRS lesions treated with laser interstitial thermal therapy;Beechar;J Neurooncol,2018

4. Laser Ablation of Abnormal Neurological Tissue Using Robotic Neuroblate System (LAANTERN): procedural safety and hospitalization;Rennert;Neurosurgery,2019

5. Magnetic resonance-guided laser interstitial thermal therapy: report of a series of pediatric brain tumors;Tovar-Spinoza;J Neurosurg Pediatr,2016

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