A prospective phase I dose-escalation trial of stereotactic ablative radiotherapy (SABR) as an alternative to cytoreductive nephrectomy for inoperable patients with metastatic renal cell carcinoma
Creators
- 1. Department of Radiation Oncology, London Regional Cancer Program, London (Canada)
- 2. Department of Medical Oncology, London Regional Cancer Program, London (Canada)
- 3. Division of Surgical Oncology, Western University, London (Canada)
- 4. Division of Urology, Western University, London (Canada)
- 5. Department of Epidemiology and Biostatistics, Western University, London (Canada)
Description
Cytoreductive nephrectomy is thought to improve survival in metastatic renal cell carcinoma (mRCC). As many patients are ineligible for major surgery, we hypothesized that SABR could be a safe alternative. In this dose-escalation trial, inoperable mRCC patients underwent SABR targeting the entire affected kidney. Toxicity (CTCAE v3.0), quality of life (QoL), renal function, and tumour response (RECIST v1.0) were assessed. Twelve patients of mostly intermediate (67%) or poor (25%) International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) prognostic class, median KPS of 70%, and median tumour size of 8.7 cm (range: 4.8–13.8) were enrolled in successive dose cohorts of 25 (n = 3), 30 (n = 6), and 35 Gy (n = 3) in 5 fractions. SABR was well tolerated with 3 grade 3 events: fatigue (2) and bone pain (1). QoL decreased for physical well-being (p = 0.016), but remained unchanged in other domains. SABR achieved a median tumour size reduction of − 17.3% (range: + 5.3 to − 54.4) at 5.3 months. All patients progressed systemically and median OS was 6.7 months. Crude median follow-up was 5.8 months. In non-operable mRCC patients, renal-ablative SABR to 35 Gy in 5 fractions yielded acceptable toxicity, renal function preservation, and stable QoL. SABR merits further prospective investigation as an alternative to cytoreductive nephrectomy. http://clinicaltrials.gov NCT02264548. Registered July 22 2014 – Retrospectively registered: https://clinicaltrials.gov/ct2/show/NCT02264548 The online version of this article (10.1186/s13014-018-0992-3) contains supplementary material, which is available to authorized users.
Availability note (English)
Available from http://dx.doi.org/10.1186/s13014-018-0992-3; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5859400Additional details
Identifiers
Publishing Information
- Journal Title
- Radiation Oncology (Online)
- Journal Volume
- 13
- Journal Page Range
- vp.
- ISSN
- 1748-717X
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 49082552
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CARCINOMAS; GY RANGE 10-100; KIDNEYS; NEPHRECTOMY; PATIENTS; RADIATION DOSES; RADIOTHERAPY
- Descriptors DEC
- ABSORBED DOSE RANGE; BODY; DISEASES; DOSES; GY RANGE; MEDICINE; NEOPLASMS; NUCLEAR MEDICINE; ORGANS; RADIATION DOSE RANGES; RADIOLOGY; SURGERY; THERAPY
Optional Information
- Copyright
- Copyright (c) The Author(s). 2018
- Notes
- PMCID: PMC5859400; PMID: 29558966; PUBLISHER-ID: 992; OAI: oai:pubmedcentral.nih.gov:5859400