onc brain

About · curated by Nick Boehling, MD · @nb2276

2026-05-19 ESTRO Congress 2026

digest generated 2026-08-11

Single-fraction SABR pooled across 3 centres: 2yr LC 90-93%, G3+ 2.9% in 1687 pts (AE denominator n=789, primary NSCLC only).
Thoracic carried the day: the largest single-fraction SABR series to date holds 2yr LC 90-93% with G3+ 2.9%, though the dose is not reported in source, so the prescription cannot be tied to the outcome. Bladder TMT (CLR 63.7%, salvage cystectomy 9.7%) and the prostate ePLND-vs-PSMA-PET round-up (47.7% of nodal mets outside the ePLND template) both bear on nodal and local-regional coverage decisions.

Prostate

Staging round-up, not new randomised data: the nodal-coverage question is whether a negative PSMA-PET licenses PLND omission when half of nodal disease sits outside the surgical template.

ePLND vs PSMA-PET staging (AUA2026 round-up)

TL;DRAUA2026 round-up: PSMA-PET NPV ~96% may allow PLND omission in intermediate risk; 47.7% of nodal mets sit outside ePLND template.

Why it mattersRadiation oncology

The RT-relevant number is toxicity sequencing: 19-29% lower limb lymphedema after PLND plus salvage pelvic nodal RT versus 0-9% after pelvic nodal RT alone, with 2-22% genital lymphedema in the combined group. If PSMA-PET is negative and PLND is omitted, later elective or salvage pelvic nodal coverage carries far less lymphedema cost.

Monday clinic

In intermediate-risk pts with a PSMA-PET negative for nodal involvement, this supports omitting PLND before planned or possible pelvic nodal RT; it does not settle the high-risk case, where the round-up calls the decision individual.

The longer read
Primary staging Ga-PSMA PET/CT in 1253 men; 47.7% of lymph node metastases outside ePLND boundaries.
Primary staging Ga-PSMA PET/CT in 1253 men; 47.7% of lymph node metastases outside ePLND boundaries.
+3 more figures
ePLND vs PSMA-PET staging (AUA2026 round-up)
TreatmentLower limb lymphedemaGenital lymphedema
RP with PLND0-14%n/a
Pelvic node RT0-9%n/a
PLND + salvage pelvic node RT19-29%2-22%
ePLND vs PSMA-PET staging (AUA2026 round-up)
ePLND vs PSMA-PET staging (AUA2026 round-up)
10 details 5 trials watching

AUA 2026 podium round-up of the ePLND question in the PSMA-PET era. Draws on a 1253-man primary staging series (Yaxley, BJUI 2019), a systematic review of lymphedema (Clinckaert, Cancers 2022), a cohort of 3544 pts (Tyritzis, J Urol 2015) and a SWOT perspective (Roberts, PCAN 2024). No new dataset.

Staging yield argues against template adequacy: 47.7% of nodal metastases fell outside ePLND boundaries. PSMA-PET NPV is given as ~96% in the source text without its parent series named.

Lymphedema tracks the combination, not either modality alone: 0-14% after RP with PLND, 0-9% after pelvic nodal RT, 19-29% after PLND plus salvage pelvic nodal RT with 2-22% genital lymphedema. LND also carried a 6-10x DVT/PE risk increase in Tyritzis.

newly diagnosed prostate cancer being staged with PSMA-PET before local therapy
Does not represent pts already node-positive on conventional imaging or those in the salvage setting.

The argument is that a template operation cannot stage what sits outside the template, so its role narrows to pts in whom imaging is likely wrong. The slide's own conclusion keeps high-risk disease individualized rather than resolved, and explicitly asks that the possibility of adjuvant or salvage pelvic RT enter that conversation.

Slide-level source: NPV ~96% has no denominator, cohort or PSMA tracer attached here, and no BCR effect size is reported for the RCTs the round-up invokes. The lymphedema review's authors note the absent uniform definition, so 19-29% is a range across heterogeneous ascertainment, not a pooled estimate.

Sourced from @RomanCarvajal

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Bladder

A 369-pt multicentre TMT cohort with no cystectomy comparator; RT dose, fractionation and target volume are absent from source, limiting transfer to practice.

Caveats dominate

Bladder-preserving TMT multicenter analysis (URONCOR)

ForcT2-T4aN0M0 MIBC treated with definitive TMT, median age 76

TL;DRCLR 63.7% in a 369-pt Spanish TMT cohort; salvage cystectomy 9.7%, image-guidance quality and 5-FU-based CRT predicted local response.

Why it mattersRadiation oncology

The modifiable RT variable here is verification protocol: weekly portal imaging carried OR 0.35 (0.20-0.60) for complete local response, with VMAT trending favorable, across a 2010 to 2022 accrual. Dose, fractionation and target volume are not reported in source, so what transfers is the case for daily volumetric IGRT in a filling, moving organ.

Monday clinic

In cT2-T4aN0M0 MIBC pts in their seventies weighing bladder preservation against cystectomy, this real-world series supports TMT delivered with modern image guidance and a 5-FU-based backbone; it does not inform node-positive or metastatic disease and carries no head-to-head against radical cystectomy.

The longer read
Bladder-preserving TMT multicenter analysis (URONCOR)
10 details

Multicenter retrospective cohort, Spain, 2010 to 2022, N=369 treated with definitive trimodality therapy (maximal TURBT then concurrent chemoradiotherapy). Predictors of response identified by multivariable logistic regression. Follow-up duration not reported in source.

cT2-T4aN0M0 MIBC selected for bladder preservation. Median age 76, 85.1% male. Fitness for cystectomy and completeness of TURBT are not reported in source.

Concurrent chemoradiotherapy, regimen at each center's discretion. 5-FU-based CRT predicted higher complete local response (OR 4.9, 95% CI 1.1-22.1, p=0.038). The comparator regimens are not named in source.

Dose, fractionation and target volume are not reported in source. The only technique signals reported are verification frequency (weekly portal imaging, OR 0.35 for CLR) and a non-significant trend favoring VMAT.

Primary: complete local response (CLR). Secondary: OS, CSS, recurrence patterns, salvage cystectomy. No OS or CSS estimate appears in the source, so the survival half of the conclusion cannot be checked.

CLR 63.7%, salvage cystectomy 9.7%. Progression 28.8%, with systemic failure (10.7%) running at or above local-only failure (10.1%).

BC2001 established the locoregional-control gain from adding chemotherapy to bladder radiotherapy, and the pooled RTOG bladder-preservation experience set the complete-response benchmark; both were protocol populations. This adds European real-world multicenter data at a median age of 76, with no internal cystectomy comparator.

cT2-T4aN0M0 MIBC pts selected for definitive TMT in routine European practice, median age 76
Does not represent node-positive or metastatic disease, nor pts triaged to upfront radical cystectomy.

No follow-up duration, OS or CSS estimate is reported, so the durability behind the preservation claim cannot be judged. The 5-FU odds ratio spans 1.1 to 22.1, compatible with a marginal or a large effect, and in a retrospective series regimen choice tracks renal function and performance status.

Systemic failure at 10.7% running at or above local-only failure at 10.1% argues the ceiling in this population is micrometastatic disease rather than the bladder, which caps what further local intensification can buy. Read conservatively, the predictors favor modern image guidance and an active concurrent backbone, not any specific verification schedule.

Retrospective multicenter cohort with no cystectomy comparator; imaging and chemo predictors come from multivariable regression across a 2010-2022 era shift, so a causal reading is unsupported.

  • Does daily volumetric IGRT improve complete local response vs weekly portal imaging?
  • Which concurrent chemotherapy backbone maximizes complete local response in TMT?
  • Long-term bladder-intact survival vs radical cystectomy in matched populations

Sourced from @URONCOR

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Thoracic / Lung

Scale, not randomisation: 1687 pts across 3 centres extend the single-fraction SABR experience without a multi-fraction comparator.

Early signal

Single-fraction SABR pooled analysis, 1687 pts

ForPrimary NSCLC or pulmonary oligomets selected for single-fraction SABR

TL;DRLocal control 90-93% at 2yr and G3+ AEs 2.9% across 1687 single-fraction SABR pts at 3 centres.

Why it mattersRadiation oncology

The oligomet read is the gap between local control and PFS: 90-93% LC at 2yr against median PFS 11 mo, so distant failure, not the treated lesion, drives the course. For primary NSCLC the same LC sits with median PFS 30 mo, which is the split that should decide whether one-visit ablation is offered as definitive treatment or as a break from systemic therapy.

Monday clinic

In early-stage primary NSCLC where visit burden drives the fractionation choice, this supports single fraction as a durable local option (LC 90-93% at 2yr, G3+ 2.9%); tumour location and operability are not reported, so who it represents stays open.

The longer read
Single-fraction SABR pooled analysis, 1687 pts
CohortnMedian PFSMedian OS
Primary NSCLC120030 mo3.5 yrs
Pulmonary oligometastases48711 mo>4 yrs
+2 more figures
Single-fraction SABR pooled analysis, 1687 pts
EndpointPrimary NSCLCOligometastases
1yr OS84% (95% CI 82, 86)90% (95% CI 86, 92)
2yr OS67% (95% CI 64, 69)75% (95% CI 71, 79)
Median OS40 mo (36, 43)51 mo (42, 58)
Single-fraction SABR pooled analysis, 1687 pts
Adverse event (n=789)n (%)
Any AE215 (27%)
Grade 2+124 (15.7%)
Grade 3+23 (2.9%)
Chest wall pain114 (14%)
Pneumonitis52 (7%)
Fatigue29 (4%)
Dyspnea13 (2%)
6 details

Pooled analysis of 1687 pts treated with single-fraction SABR at three centres (Peter MacCallum, Cleveland Clinic, Roswell Park): 1200 primary NSCLC and 487 pulmonary oligometastases. Whether the contributing cohorts were prospective or retrospective is not stated in source.

Eligibility, operability, tumour size and central vs peripheral location are not reported in source. Cohort mix differs sharply by centre: Roswell Park supplied 401 of the NSCLC pts but only 34 oligomet pts, while Peter Mac supplied 283 of 487 oligomet pts.

Single fraction throughout, but the prescribed dose is not reported in source. Without it the outcome cannot be mapped onto a schedule a reader could write, which is the one parameter that would carry this into planning.

No primary endpoint is stated in the source. Reported outcomes are local control, freedom from local failure, PFS, OS and adverse events, each descriptive rather than tested against a comparator.

Local control 90-93% at 2 years across both cohorts, with isolated local or locoregional failure described as very uncommon. Survival separates by cohort while local outcome does not.

CentrePrimary NSCLCPulmonary oligomets
Cleveland Clinic576170
Peter MacCallum223283
Roswell Park40134

AE reporting covers 789 primary NSCLC pts only, with no Roswell Park data and no oligometastasis toxicity in source. Within that subset chest wall pain and pneumonitis dominate and G3+ events stay at 2.9%.

Single-fraction SABR already carries randomised support: RTOG 0915 in peripheral early-stage NSCLC and SAFRON II in pulmonary oligometastases, both randomised single against multi-fraction schedules. This series adds scale and follow-up at three high-volume centres, which is what a non-randomised dataset can contribute, and no comparator.

pts selected for single-fraction SABR to a primary NSCLC or a pulmonary oligometastasis at three high-volume centres
Does not represent pts treated with multi-fraction schedules, nor any population defined by operability or tumour location, neither of which the source reports.

Toxicity rests on 789 of 1687 pts, with one centre absent from the AE table and the oligometastatic cohort not represented in it at all. Centre mix is uneven, so pooled rates carry each centre's own selection rather than a common one.

The question the thread raises, whether one-stop SABR should be used more often, is not the question this dataset answers. What it does show is that local control near 90-93% and G3+ toxicity near 3% hold at scale outside a protocol, which is the usual worry about a schedule with no second chance. The unreported dose sits between that reassurance and a prescription.

Pooled uncontrolled series across three centres, no multi-fraction comparator and no stated design; dose unreported, so outcomes cannot be tied to a prescription.

  • Whether single-fraction outcomes hold for central tumours
  • Durability of single-fraction ablation for pulmonary oligometastases beyond first progression
  • Toxicity of single-fraction SABR in the oligometastatic cohort

Sourced from @_ShankarSiva

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