Evidence map›Paper›PMID 36942088›Full record

ArticleClinical and translational radiation oncology2023

Feasibility of biology-guided radiotherapy for metastatic renal cell carcinoma driven by PSMA PET imaging.

Mathieu Gaudreault, David Chang, Nicholas Hardcastle, Lachlan McIntosh, Price Jackson, Tomas Kron, Cristian Udovicich, Michael S Hofman, Shankar Siva

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational radiation oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Who cites it

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Nuclear medicine and molecular imaging · 2023
    Article
  4. Review
  5. Review
4 · The record

Corrections and comments

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

9 authors at 2 institutions in 1 country.

Mathieu GaudreaultDepartment of Physical Sciences, Peter MacCallum Cancer Centre, Melbourne, Victoria 3000, Australia.
David ChangSir Peter MacCallum Department of Oncology, The University of Melbourne, Victoria 3010, Australia.
Nicholas HardcastleDepartment of Physical Sciences, Peter MacCallum Cancer Centre, Melbourne, Victoria 3000, Australia.
Lachlan McIntoshDepartment of Physical Sciences, Peter MacCallum Cancer Centre, Melbourne, Victoria 3000, Australia.
Price JacksonDepartment of Physical Sciences, Peter MacCallum Cancer Centre, Melbourne, Victoria 3000, Australia.
Tomas KronDepartment of Physical Sciences, Peter MacCallum Cancer Centre, Melbourne, Victoria 3000, Australia.
Cristian UdovicichSir Peter MacCallum Department of Oncology, The University of Melbourne, Victoria 3010, Australia.
Michael S HofmanSir Peter MacCallum Department of Oncology, The University of Melbourne, Victoria 3010, Australia.
Shankar SivaSir Peter MacCallum Department of Oncology, The University of Melbourne, Victoria 3010, Australia.
The University of Melbourne · AUPeter MacCallum Cancer Centre · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Biology-guided radiotherapy (BgRT) is a novel treatment where the detection of positron emission originating from a volume called the biological tracking zone (BTZ) initiates dose delivery. Prostate-specific membrane antigen (PSMA) positron emission tomography (PET) is a novel imaging technique that may improve patient selection for metastasis-directed therapy in renal cell carcinoma (RCC). This study aims to determine the feasibility of BgRT treatment for RCC. Material and methods: All consecutive patients that underwent PSMA PET/CT scan for RCC staging at our institution between 2014 and 2020 were retrospectively considered for inclusion. GTVs were contoured on the CT component of the PET/CT scan. The tumor-to-background ratio was quantified from the normalized standardized uptake value (nSUV), defined as the ratio between SUVmax inside the GTV and SUVmean inside the margin expansion. Tumors were classified suitable for BgRT if (1) nSUV was greater or equal to an nSUV threshold and (2) if the BTZ was free of any PET-avid region other than the tumor. Results: Out of this cohort of 83 patients, 47 had metastatic RCC and were included in this study. In total, 136 tumors were delineated, 1 to 22 tumors per patient, mostly in lung (40%). Using a margin expansion of 5 mm/10 mm/20 mm and nSUV threshold = 3, 66%/63%/41% of tumors were suitable for BgRT treatment. Uptake originating from another tumor, the kidney, or the liver was typically inside the BTZ in tumors judged unsuitable for BgRT. Conclusions: More than 60% of tumors were found to be suitable for BgRT in this cohort of patients with RCC. However, the proximity of PET-avid organs such as the liver or the kidney may affect BgRT delivery.

Indexed as

Abdo, abdomenBgRTBgRT, biology-guided radiotherapyBTZBTZ, biological tracking zoneGTV, gross tumor volumeLN&ST, lymph node and soft tissueMIP, maximum intensity projectionnSUV, normalized SUVPET, positron emission tomographyPSMAPSMA, prostate specific membrane antigenRCCRCC, renal cell carcinomaSUV, standardized uptake valueTPS, treatment planning system

Identifiers

PMID36942088
PMCPMC10023908
OpenAlexW4322505797

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.