Definitive radiotherapy in lieu of systemic therapy for oligometastatic renal cell carcinoma: a single-arm, single-centre, feasibility, phase 2 trial
- PMID: 34717797
- PMCID: PMC11975425
- DOI: 10.1016/S1470-2045(21)00528-3
Definitive radiotherapy in lieu of systemic therapy for oligometastatic renal cell carcinoma: a single-arm, single-centre, feasibility, phase 2 trial
Abstract
Background: The role of radiotherapy in metastatic renal cell carcinoma is controversial. We prospectively tested the feasibility and efficacy of radiotherapy to defer systemic therapy for patients with oligometastatic renal cell carcinoma.
Methods: This single-arm, phase 2, feasibility trial was done at one centre in the USA (The MD Anderson Cancer Center, Houston, TX, USA). Patients (aged ≥18 years) with five or fewer metastatic lesions, an Eastern Cooperative Oncology Group status of 0-2, and no more than one previous systemic therapy (if this therapy was stopped at least 1 month before enrolment) without limitations on renal cell carcinoma histology were eligible for inclusion. Patients were treated with stereotactic body radiotherapy (defined as ≤5 fractions with ≥7 Gy per fraction) to all lesions and maintained off systemic therapy. When lesion location precluded safe stereotactic body radiotherapy, patients were treated with hypofractionated intensity-modulated radiotherapy regimes consisting of 60-70 Gy in ten fractions or 52·5-67·5 Gy in 15 fractions. Additional rounds of radiotherapy were allowed to treat subsequent sites of progression. Co-primary endpoints were feasibility (defined as all planned radiotherapy completed with <7 days unplanned breaks) and progression-free survival. All efficacy analyses were intention-to-treat. Safety was analysed in the as-treated population. A second cohort, with the aim of assessing the feasibility of sequential stereotactic body radiotherapy alone in patients with low-volume metastatic disease, was initiated and will be reported separately. This study is registered with ClinicalTrials.gov, NCT03575611.
Findings: 30 patients (six [20%] women) were enrolled from July 13, 2018, to Sept 18, 2020. All patients had clear cell histology and had a nephrectomy before enrolment. All patients completed at least one round of radiotherapy with less than 7 days of unplanned breaks. At a median follow-up of 17·5 months (IQR 13·2-24·6), median progression-free survival was 22·7 months (95% CI 10·4-not reached; 1-year progression-free survival 64% [95% CI 48-85]). Three (10%) patients had severe adverse events: two grade 3 (back pain and muscle weakness) and one grade 4 (hyperglycaemia) adverse events were observed. There were no treatment-related deaths.
Interpretation: Sequential radiotherapy might facilitate deferral of systemic therapy initiation and could allow sustained systemic therapy breaks for select patients with oligometastatic renal cell carcinoma.
Funding: Anna Fuller Foundation, the Cancer Prevention and Research Institute of Texas (CPRIT), and the National Cancer Institute.
Copyright © 2021 Elsevier Ltd. All rights reserved.
Conflict of interest statement
Declaration of interests CT is an editor of Pocket Radiation Oncology: the MD Anderson Handbook of Radiation Oncology and receives royalties from Wolters Kluwer Health for book sales; royalties from the Stanford Office of Technology and licensing for US patent number 9 175 079; and travel support from AstraZeneca. PM reports honoraria for scientific advisory boards membership for Mirati Therapeutics, Bristol-Myers Squibb, and Exelixis; consulting fees from Axiom Healthcare; non-branded educational programmes supported by Exelixis and Pfizer; and research funding from Takeda, Bristol-Myers Squibb, Mirati, and Gateway for Cancer Research. AYS reports honoraria for scientific advisory boards membership from Bristol-Myers Squibb, Exelixis, and Pfizer. EJ reports grants from Merck, NiKang, and Novartis; consulting fees from Aveo, Aravive, Calithera, Eisai, Exelixis, Ipsen, Merick, NiKang, and Novartis; and is the Vice Chair of the National Comprehensive Cancer Network kidney cancer guidelines committee and board member of the International Kidney Cancer Coalition (both unpaid). NMT reports grants from Bristol-Myers Squibb, Nektar, Calithera, Arrowhead, Eisai, and Novartis; and consulting fees from Bristol-Myers Squibb, Pfizer, Nektar, Exelixis, Eisai, Eli Lilly, Oncorena, Calithera, Surface Oncology, Novartis, Ipsen, Merck. All other authors declare no competing interests.
Figures
Comment in
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SBRT feasible for oligometastatic RCC.Nat Rev Clin Oncol. 2022 Jan;19(1):6. doi: 10.1038/s41571-021-00582-1. Nat Rev Clin Oncol. 2022. PMID: 34759356 No abstract available.
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Oligometastatic renal cell carcinoma: radiotherapy as a new standard of care?Lancet Oncol. 2021 Dec;22(12):1644-1645. doi: 10.1016/S1470-2045(21)00665-3. Lancet Oncol. 2021. PMID: 34856135 No abstract available.
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[Stereotactic body radiotherapy as "first-line treatment" for oligometastatic renal cell cancer].Strahlenther Onkol. 2022 May;198(5):497-499. doi: 10.1007/s00066-022-01920-7. Epub 2022 Mar 12. Strahlenther Onkol. 2022. PMID: 35278095 German. No abstract available.
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Radiation Therapy for Renal Cell Carcinoma.Int J Radiat Oncol Biol Phys. 2023 Nov 1;117(3):523-525. doi: 10.1016/j.ijrobp.2023.03.073. Int J Radiat Oncol Biol Phys. 2023. PMID: 37739599 No abstract available.
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