Early and Midtreatment Mortality in Palliative Radiotherapy: Emphasizing Patient Selection in High-Quality End-of-Life Care

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Matthew S. Ning Department of Radiation Oncology, and

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Prajnan Das Department of Radiation Oncology, and

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David I. Rosenthal Department of Radiation Oncology, and

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Bouthaina S. Dabaja Department of Radiation Oncology, and

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Zhongxing Liao Department of Radiation Oncology, and

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Joe Y. Chang Department of Radiation Oncology, and

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Daniel R. Gomez Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York;

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Ann H. Klopp Department of Radiation Oncology, and

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G. Brandon Gunn Department of Radiation Oncology, and

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Pamela K. Allen Department of Radiation Oncology, and

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Paige L. Nitsch Radiation Physics, The University of Texas MD Anderson Cancer Center, Houston, Texas;

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Rachel B. Natter Department of Radiation Oncology, and

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Tina M. Briere Radiation Physics, The University of Texas MD Anderson Cancer Center, Houston, Texas;

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Joseph M. Herman Department of Radiation Medicine, Zucker School of Medicine at Hofstra/Northwell, Lake Success, New York.

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Rebecca Wells Department of Management, Policy, and Community Health, University of Texas Health Science Center School of Public Health, Houston, Texas; and

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Albert C. Koong Department of Radiation Oncology, and

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Mary Frances McAleer Department of Radiation Oncology, and

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Background: Palliative radiotherapy (RT) is effective, but some patients die during treatment or too soon afterward to experience benefit. This study investigates end-of-life RT patterns to inform shared decision-making and facilitate treatment consistent with palliative goals. Materials and Methods: All patients who died ≤6 months after initiating palliative RT at an academic cancer center between 2015 and 2018 were identified. Associations with time-to-death, early mortality (≤30 days), and midtreatment mortality were analyzed. Results: In total, 1,620 patients died ≤6 months from palliative RT initiation, including 574 (34%) deaths at ≤30 days and 222 (14%) midtreatment. Median survival was 43 days from RT start (95% CI, 41–45) and varied by site (P<.001), ranging from 36 (head and neck) to 53 days (dermal/soft tissue). On multivariable analysis, earlier time-to-death was associated with osseous (hazard ratio [HR], 1.33; P<.001) and head and neck (HR, 1.45; P<.001) sites, multiple RT courses ≤6 months (HR, 1.65; P<.001), and multisite treatments (HR, 1.40; P=.008), whereas stereotactic technique (HR, 0.77; P<.001) and more recent treatment year (HR, 0.82; P<.001) were associated with longer survival. No difference in time to death was noted among patients prescribed conventional RT in 1 to 10 versus >10 fractions (median, 40 vs 47 days; P=.272), although the latter entailed longer courses. The 30-day mortality group included 335 (58%) inpatients, who were 27% more likely to die midtreatment (P=.031). On multivariable analysis, midtreatment mortality among these inpatients was associated with thoracic (odds ratio [OR], 2.95; P=.002) and central nervous system (CNS; OR, 2.44; P=.002) indications, >5-fraction courses (OR, 3.27; P<.001), and performance status of 3 to 4 (OR, 1.63; P=.050). Conversely, palliative/supportive care consultation was associated with decreased midtreatment mortality (OR, 0.60; P=.045). Conclusions: Earlier referrals and hypofractionated courses (≤5–10 treatments) should be routinely considered for palliative RT indications, given the short life expectancies of patients at this stage in their disease course. Providers should exercise caution for emergent thoracic and CNS indications among inpatients with poor prognoses due to high midtreatment mortality.

Submitted April 24, 2020; final revision received August 31, 2020; accepted for publication September 28, 2020. Published online April 20, 2021.

Previous presentation: Presented as an oral abstract at the 2019 ASTRO Annual Meeting; September 15–18, 2019; Chicago, Illinois. Abstract 1084.

Author contributions: Study concept and design: Ning, McAleer. Data acquisition: Ning, Das, Rosenthal, Chang, Allen, Briere, Wells, McAleer. Data analysis and interpretation: Ning, Das, Rosenthal, Chang, Allen, Briere, Wells, McAleer. Manuscript preparation: All authors. Critical revision: All authors.

Disclosures: Dr. Herman reports receiving consulting fees from 1440 Foundation and Medtronic. The remaining authors have disclosed that they have not received any financial consideration from any person or organization to support the preparation, analysis, results, or discussion of this article.

Funding: Research reported in this article was supported in part by the NIH/NCI Cancer Center Support (Core) grant CA016672 to The University of Texas MD Anderson Cancer Center.

Disclaimer: The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.

Correspondence: Matthew S. Ning, MD, MPH, Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Unit 0097, 1515 Holcombe Boulevard, Houston, TX 77030. Email: msning@mdanderson.org
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