Association of Long-term Outcomes With Stereotactic Radiosurgery vs Whole-Brain Radiotherapy for Resected Brain Metastasis

Author:

Palmer Joshua D.1,Klamer Brett G.2,Ballman Karla V.34,Brown Paul D.5,Cerhan Jane H.5,Anderson S. Keith3,Carrero Xiomara W.3,Whitton Anthony C.6,Greenspoon Jeffrey6,Parney Ian F.5,Laack Nadia N.I.5,Ashman Jonathan B.7,Bahary Jean-Paul8,Hadjipanayis Costas G.9,Urbanic James J.10,Barker Fred G.11,Farace Elana12,Khuntia Deepak13,Giannini Caterina5,Buckner Jan C.5,Galanis Evanthia5,Roberge David8

Affiliation:

1. The James Cancer Center at The Ohio State University, Columbus

2. Center for Biostatistics, The Ohio State University, Columbus

3. Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, Minnesota

4. Weill Cornell Medicine, New York, New York

5. Mayo Clinic, Rochester, Minnesota

6. Juravinski Cancer Centre, Hamilton, Ontario, Canada

7. Mayo Clinic, Phoenix/Scottsdale, Arizona

8. CHUM, Montreal, Quebec, Canada

9. Mount Sinai Beth Israel, New York, New York

10. University of California, San Diego, Moores Cancer Center, La Jolla, California

11. Massachusetts General Hospital Cancer Center, Boston, Massachusetts

12. Penn State University College of Medicine, Hershey, Pennsylvania

13. Precision Cancer Specialists and Varian Medical Systems, Palo Alto, California

Abstract

ImportanceLong-term outcomes of radiotherapy are important in understanding the risks and benefits of therapies for patients with brain metastases.ObjectiveTo determine how the use of postoperative whole-brain radiotherapy (WBRT) or stereotactic radiosurgery (SRS) is associated with quality of life (QOL), cognitive function, and intracranial tumor control in long-term survivors with 1 to 4 brain metastases.Design, Setting, and ParticipantsThis secondary analysis of a randomized phase 3 clinical trial included 48 institutions in the US and Canada. Adult patients with 1 resected brain metastases but limited to those with 1 to 4 brain metastasis were eligible. Unresected metastases were treated with SRS. Long-term survivors were defined as evaluable patients who lived longer than 1 year from randomization. Patients were recruited between July 2011 and December 2015, and data were first analyzed in February 2017. For the present study, intracranial tumor control, cognitive deterioration, QOL, and cognitive outcomes were measured in evaluable patients who were alive at 12 months from randomization and reanalyzed in June 2017.InterventionsStereotactic radiosurgery or WBRT.Main Outcomes and MeasuresIntracranial tumor control, toxic effects, cognitive deterioration, and QOL.ResultsFifty-four patients (27 SRS arm, 27 WBRT arm; female to male ratio, 65% vs 35%) were included for analysis with a median follow-up of 23.8 months. Cognitive deterioration was less frequent with SRS (37%-60%) compared with WBRT (75%-91%) at all time points. More patients declined by 2 or more standard deviations (SDs) in 1 or more cognitive tests for WBRT compared with SRS at 3, 6, and 9 months (70% vs 22%, 46% vs 19%, and 50% vs 20%, respectively). A 2 SD decline in at least 2 cognitive tests was associated with worse 12-month QOL in emotional well-being, functional well-being, general, additional concerns, and total scores. Overall QOL and functional independence favored SRS alone for categorical change at all time points. Total intracranial control for SRS alone vs WBRT at 12 months was 40.7% vs 81.5% (difference, −40.7; 95% CI, −68.1% to −13.4%), respectively. Data were first analyzed in February 2017.Conclusions and RelevanceThe use of SRS alone compared with WBRT resulted in less cognitive deterioration among long-term survivors. The association of late cognitive deterioration with WBRT was clinically meaningful. A significant decline in cognition (2 SD) was associated with overall QOL. However, intracranial tumor control was improved with WBRT. This study provides detailed insight into cognitive function over time in this patient population.Trial RegistrationClinicalTrials.gov Identifier: NCT01372774; ALLIANCE/CCTG: N107C/CEC.3 (Alliance for Clinical Trials in Oncology/Canadian Cancer Trials Group)

Publisher

American Medical Association (AMA)

Subject

Oncology,Cancer Research

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