Evidence map›Paper›PMID 41458679›Full record

ArticleCureus2025

How to Safely Deliver Stereotactic Ablative Radiotherapy With High-Dose or Multi-agent Systemic Therapy.

Mark E Bernard

Abstract read
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Mark E BernardRadiation Oncology, University of Kentucky, Lexington, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhile systemic therapy remains the backbone treatment for patients with stage IV cancer, local ablative treatments are often given to improve survival. Common local ablative treatments consist of stereotactic ablative radiotherapy (SABR), surgical metastasectomy, or interventional ablative techniques. SABR has the advantage of being able to give treatment without pausing systemic therapy. AIMS AND

objectivesThis study serves to evaluate the efficacy of SABR given concurrently with high-dose and multi-agent systemic therapy during the off week of systemic therapy.

methodsA retrospective review of patients between 2023 and 2025 treated with systemic therapy with concurrent SABR during the off week of systemic therapy was conducted. Radiation-induced side effects were analyzed using Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.

resultsSix patients with 12 lesions were included in this study. The five different systemic therapy agents used were 1. carboplatin and paclitaxel and pembrolizumab (one patient), 2. fluorouracil & panitumumab (one patient), 3. capecitabine (one patient), 4. FOLFIRI (folinic acid, fluorouracil, and irinotecan) (two patients), and 5. 5-FOLFIRINOX (folinic acid, fluorouracil, irinotecan, and oxaliplatin) (one patient). Four patients were oligometastatic, and two were oligoprogressive. The most common SABR target was the lung, and the most common SABR regimen was 45 Gy in three fractions. Median planning target volume (PTV) was 10cc. The median time from the last systemic therapy infusion to SBRT was seven days. The median time from the last SBRT fraction to the next systemic therapy infusion was one day. Median follow-up was 7.3 months. There were no grade three or higher toxicities reported. One patient had grade one radiation side effects consisting of pain. One patient had diarrhea described as being mild and considered to be grade one. Out of the twelve lesions treated, there were three distant failures and one local/regional failure. Median overall survival was 18.9 months.

conclusionSABR given concurrently with multi-agent and high-dose systemic therapy during the off week of therapy is a safe and efficacious option. This treatment technique allows patients to remain on systemic therapy without any interruptions. Therefore, SABR can be a preferred local ablative treatment for patients with oligometastatic and oligoprogressive cancer while on concurrent systemic therapy.

Indexed as

concurrentoilgoprogressiveoligometastaticsbrtsystemic therapy

Identifiers

PMID41458679
PMCPMC12742234

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.