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About · curated by Nick Boehling, MD · @nb2276

2026-07-31

Consensus

IROCK Contouring Guidelines (RCC SABR)

ForLocalized RCC considered for SABR, including IVC thrombus, post-RN or post-RFA recurrence

TL;DRFirst international consensus contouring atlas for RCC SABR: median DSC 0.85 across 16 experts, 4 scenario-specific iGTV statements.

Why it mattersRadiation oncology

The two hardest scenarios are named and quantified: Case 1 (IVC thrombus) and Case 4 (post-RFA cavity) carried the worst agreement (DSC 0.85 and 0.75, HD 64.60 and 9.00 mm), driven by how far superiorly thrombus was covered and how much cavity was included. Both statements push toward larger volumes, so OAR priority and a 5 mm PTV are the gates on whether that transfers.

Monday clinic

In a patient with post-RFA residual RCC or an IVC tumor thrombus being planned for SABR, this defines the target as the whole ablation cavity or the full thrombus rather than the visible nodule alone; it does not address dose selection or whether SABR beats nephrectomy.

The longer read
12 details

International contouring consensus under IROCK, convened at ASTRO 2023. 16 radiation oncologists contoured 4** RCC SABR scenarios on CT alone via EduCase; a STAPLE algorithm generated the 95% consensus contour, refined across 2 online meetings in May and June 2024. Statements were revised to uniform (100%) agreement**.

Panelists, not patients: inclusion required ≥10 prior RCC SABR cases, with 14 of 16 having treated ≥10 in the preceding 12 months. Cases were a >10 cm RCC with IVC tumor thrombus, a central tumor abutting the hilum, a local recurrence post-nephrectomy, and a post-RFA cavity recurrence.

Target is the iGTV (GTV incorporating internal motion); no participant added a microscopic-spread margin, so no separate ITV is recommended. The most common PTV expansion was a uniform 5 mm, predicated on supine vacuum-cushion setup, 4D-CT sim, IV contrast and daily CBCT. Dose objectives and OAR constraints for 1, 3, or 5 fractions are tabulated from FASTRACK-II and AQuOS-II.

Overall median DSC 0.85 (range 0.40-0.95), median MDA 2.17 mm (0.71-10.82), median HD 9.00 mm (4.00-89.31), with DSC above 0.70 in every case. Two-way ANOVA showed all three metrics differed by case (P < .05); only MDA differed by participant (P = .03).

CaseDSCMDA (mm)HD (mm)
1: >10 cm RCC + IVC thrombus0.85, 0.79-0.856.69, 5.88-8.7964.60, 64.44-86.40
2: central tumor at hilum0.90, 0.84-0.931.55, 1.00-2.097.92, 5.35-9.98
3: local recurrence post-RN0.91, 0.88-0.931.42, 1.18-1.896.18, 6.00-7.12
4: post-RFA cavity recurrence0.75, 0.60-0.792.50, 2.12-2.999.00, 9.00-12.39
localized RCC being planned for SABR at centers with 4D-CT, contrast and daily CBCT, including thrombus, post-nephrectomy and post-ablation scenarios
Does not represent metastatic RCC, cytoreductive or palliative renal RT, or centers without image-guided SABR capability and multidisciplinary urology/radiology support.

IROCK previously supplied the outcome evidence (its pooled international analyses and the FASTRACK-II phase 2), and both showed heterogeneous dose, fractionation and planning conventions across contributing centers. This fills the delineation gap those datasets left open, and it borrows its constraint table from FASTRACK-II and the ongoing AQuOS-II rather than deriving new dose-response thresholds.

The renal substructure question is left deliberately unsettled: cortex is defined for use, hilum is explicitly not a dose-limiting OAR, on the reasoning that sparing an unvalidated structure would redistribute dose into parenchyma that does correlate with renal function. AQuOS-II is the trial that may resolve it.

CT-only images were supplied on purpose, for international accessibility, so measured variation likely overstates what an MRI-equipped center would see. Participants never recontoured post-consensus, so the guideline's own effect on agreement is unmeasured, and adoption assumes urology, radiology and nephrology collaboration plus advanced planning technology.

Expert consensus atlas, not an outcome study: 16-panel STAPLE contours with unanimous statements, no efficacy or toxicity endpoint, unvalidated prospectively.

  • Does renal hilum sparing reduce artery stenosis or ureteric stricture?
  • Does guideline adherence improve local control or reduce toxicity?
  • Would MRI-based simulation narrow contour variability?
📚 Sources · 📄 1 paper
📄 PAPER Dhar, Aneesh; Siva, Shankar; Tan, Vivian S. et al. · International Journal of Radiation Oncology*Biology*Physics (2026-05)
International Radiosurgery Oncology Consortium of the Kidney (IROCK) Contouring Guidelines for Renal Cell Carcinoma Treated With Stereotactic Ablative Radiation Therapy

2026-05-18 ESTRO Congress 2026

Early signal

FASTRACK II NCT02613819

ForPrimary RCC ≤10cm, T1b-dominant, medically inoperable or declined surgery

Freedom from local progression local control

100% at 36, 60, 84 mo

ITT population, RECIST-assessed, median f/u 62 mo

TL;DR100% freedom from local progression at 36, 60, and 84mo after single-fraction 26Gy or 42Gy/3fx SABR in inoperable primary RCC.

Why it mattersRadiation oncology

The transferable detail is the size-adapted prescription: 26Gy in one fraction under 4cm, 42Gy/3fx above it, with median tumour 46mm and 65% T1b or higher. That is a larger-tumour cohort than most ablation series, and zero local failures out to 84mo supports offering SABR when a 77-year-old is turned down for nephrectomy.

Monday clinic

In a medically inoperable or surgery-declining patient with a primary RCC up to 10cm, including T1b and larger where thermal ablation is a poor fit, this supports SABR as a durable local option; it does not speak to the operable patient, where nephrectomy remains untested against it.

The longer read
10 details

Non-randomised phase 2, eight hospitals in Australia and the Netherlands, run by TROG and ANZUP. Enrolment July 28 2016 to Feb 27 2020; 71 enrolled, one withdrew consent before treatment. This report is the pre-planned final follow-up at a median of 62 months (IQR 60-72).

Histologically confirmed primary RCC, medically inoperable, high risk, or declined surgery, ECOG ≤2, tumours ≤10 cm, N0-N1. Median age 77 years (70-82), 49 (70%) male. Median tumour size 46 mm (37-55), with 39 (56%) T1b, six (9%) T2a and one (1%) T3a.

Size-adapted prescription: 26 Gy in a single fraction for tumours ≤4 cm, 42 Gy in three fractions 48 h apart for tumours >4 cm. Histological confirmation was required before treatment, so this is a biopsy-proven cohort rather than a radiographic-diagnosis one.

Primary: freedom from local progression by RECIST, assessed in the intention-to-treat population, as was safety.

100% local control at 36, 60 and 84 months, with no local recurrences and no cancer-related deaths reported in the cohort.

Seven (10%) patients had at least one treatment-related grade 3 event within 9 months: pain in four (6%), nausea and vomiting in three (4%), colonic obstruction in two (3%), diarrhoea in one (1%). No grade 4 events and no treatment-related deaths; no new long-term safety signals emerged with extended follow-up.

biopsy-proven primary RCC up to 10 cm in pts who are inoperable, high surgical risk, or decline surgery, median age 77 and predominantly T1b or higher
Does not represent the operable patient choosing between SABR and partial nephrectomy, nor the small renal mass under 4 cm where thermal ablation is already established.

A 100% point estimate in 70 pts carries a wide confidence bound that the headline hides, and RECIST is an imperfect local-control instrument after ablative RT, where a treated mass commonly persists without viable tumour. Renal function trajectory, the endpoint that actually competes with nephrectomy, is not reported in this source.

Prior SABR evidence in primary RCC was retrospective and pooled, so a prospective multicentre dataset at 84 months is the new contribution rather than the effect size itself. Comparison to partial nephrectomy and thermal ablation remains indirect: no randomised trial has run, and this cohort was selected against surgery by definition.

The finding that transfers is durability at a tumour size where thermal ablation performs worst, with a median of 46 mm and 65% at least T1b. What it does not settle is whether SABR is a choice rather than a fallback, which needs a randomised or matched comparison in operable pts, with renal function as a co-primary.

Single-arm phase 2, N=70, inoperable or surgery-declining pts only. No randomised comparator vs partial nephrectomy or thermal ablation. Maturity gate holds despite 62mo f/u.

  • SABR vs partial nephrectomy in operable pts
  • Renal function trajectory after SABR vs nephrectomy
  • SABR vs thermal ablation in T1b tumours
📚 Sources · 📄 1 paper
📄 PAPER Siva; Pryor; Martin et al. · The Lancet. Oncology (2026-05)
Long-term outcomes of stereotactic ablative body radiotherapy for primary kidney cancer (TROG 15.03 FASTRACK II): a multicentre, non-randomised, phase 2 study.
Abstract
BACKGROUND: Stereotactic ablative body radiotherapy (SABR) is an emerging, non-invasive alternative for primary renal cell carcinoma. We aimed to provide the final long-term trial outcomes of TransTasman Radiation Oncology Group (TROG) 15.03 FASTRACK II, the first phase 2 trial investigating SABR for primary renal cell carcinoma to our knowledge.<br/><br/>METHODS: FASTRACK II was a non-randomised, phase 2 study conducted in eight hospitals in Australia and the Netherlands by TROG and the Australian and New Zealand Urogenital and Prostate (ANZUP) Cancer Trials Group. Here, we report the final pre-planned follow-up results. Adult patients (aged &#x2265;18 years) with histologically confirmed primary renal cell carcinoma, who were medically inoperable, high risk, or declined surgery, had an Eastern Cooperative Oncology Group performance status of 2 or less, had tumours 10 cm or less in size, and had N0-N1 disease were included. Patients underwent either a single fraction SABR of 26 Gy for tumours 4 cm or less in maximum diameter, or 42 Gy in three fractions delivered 48 h apart for tumours more than 4 cm in maximum diameter. The primary outcome was freedom from local progression to assess local control after SABR evaluated with the Response Evaluation Criteria in Solid Tumours. The primary endpoint and safety were evaluated in the intention-to-treat population. A patient representative was involved in the study design and conduct. The trial was registered with ClinicalTrials.gov (NCT02613819) and is closed to enrolment.<br/><br/>FINDINGS: Between July 28, 2016, and Feb 27, 2020, 71 patients were enrolled and one withdrew consent before treatment. Median follow-up was 62 months (IQR 60-72), median age was 77 years (70-82). 49 (70%) of 70 patients were male and 21 (30%) were female. Race and ethnicity data were not collected. The median tumour size was 46 mm (37-55), with 24 (34%) patients with T1a disease, 39 (56%) with T1b disease, six (9%) with T2a disease, and one (1%) with T3a disease. One patient (1%) had nodal involvement (N1). SABR resulted in 100% local control at 36 months, 60 months, and 84 months. Seven (10%) patients had at least one grade 3 adverse event within 9 months of SABR that was designated possibly, probably, or definitely related to treatment: nausea and vomiting (three [4%] events); abdominal, flank, or tumour pain (four [6%]); colonic obstruction (two [3%]); and diarrhoea (one [1%]). No new long-term safety signals, grade 4 events, or treatment-related deaths were noted.<br/><br/>INTERPRETATION: Long-term follow-up supports the safety and local control of SABR for non-surgical patients with renal cell carcinoma, with no observed local recurrences or cancer-related deaths in this cohort, which had predominantly T1b disease or higher.<br/><br/>FUNDING: The Cancer Australia Priority-driven Collaborative Cancer Research Scheme and Varian.
📝 Siva S, Pryor D, Martin J, Hardcastle N, Moon D, Kron T, Higgs B, Foroudi F, Ruben J, Sridharan S, Montgomery R, Davey R, Lin C, Shaw M, Lawrentschuk N, Appu S, Vanneste BGL, Hofman MS, Murphy DG, De Abreu Lourenco R, Mancuso P, Brook NR, Raman A, Wong LM, Sidhom M, Wood S, Ali M, Bressel M. Long-term outcomes of stereotactic ablative body radiotherapy for primary kidney cancer (TROG 15.03 FASTRACK II): a multicentre, non-randomised, phase 2 study. Lancet Oncol. 2026 May 17:S1470-2045(26)00091-4.

2026-05-17 ESTRO Congress 2026

Unclear

RCC SBRT (5-year local control)

ForPrimary RCC treated with SBRT; stage and operability not stated in source

TL;DR100% local control at 5 years for RCC treated with SBRT, per a conference slide; no N, dose, or CI in source.

7 details

Not reported in source. The tweet gives a 5-year local control figure with no study type, N, institution, or registry identifier, so design cannot be inferred.

SBRT to primary RCC; dose, fractionation, number of fractions, and target definition are not reported in source. These are the parameters that gate transfer to practice, and none are available here.

100% local control at 5 years as stated in the source tweet. No confidence interval, no n-at-risk, and no statement of whether this is a Kaplan-Meier estimate or a crude proportion.

Beyond the missing design, the specific risk is effective follow-up: a medically inoperable RCC cohort loses pts to non-cancer death well before 5y, so a 100% figure can rest on very few pts at risk. Local control definition (RECIST-style size change vs absence of growth vs biopsy) is also unstated and swings the estimate.

Single tweet with one number, no N, design, dose, or LC definition. Cannot judge whether the 100% figure reflects efficacy or short effective follow-up.

  • Dose and fractionation behind the reported 5-year local control
  • Local control definition and n-at-risk at 5 years
  • SBRT vs partial nephrectomy in operable primary RCC
📚 Sources · 🐦 1 tweet