Evidence map›Paper›PMID 38778822›Full record

ArticleAdvances in radiation oncology2024

A Prospective Trial of Single-Fraction Radiation to the Tumor Bed with a Novel Breast-Specific Stereotactic Radiation Therapy Device: The GammaPod.

Elizabeth M Nichols, Søren M Bentzen, Meghan Milburn, Susan B Kesmodel, Emily Bellavance, Stewart J Becker, Yildirim Mutaf, Katherine Tkaczuk, Paula Rosenblatt, Steven J Feigenberg

Abstract read
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Article in Advances in radiation oncology, 2024. 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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Elizabeth M NicholsDepartment of Radiation Oncology, University of Maryland School of Medicine, Baltimore, Maryland.
Søren M BentzenDepartment of Radiation Oncology, University of Maryland School of Medicine, Baltimore, Maryland.
Meghan MilburnAnn Arundel Medical Center, Bowie, Maryland.
Susan B KesmodelUniversity of Miami Hospital and Clinics, Miami, Florida.
Emily BellavanceUniversity of Maryland School of Medicine, Baltimore, Maryland.
Stewart J BeckerUniversity of Maryland School of Medicine, Baltimore, Maryland.
Yildirim MutafKaiser Permanente, Dublin, California.
Katherine TkaczukUniversity of Maryland School of Medicine, Baltimore, Maryland.
Paula RosenblattUniversity of Maryland School of Medicine, Baltimore, Maryland.
Steven J FeigenbergPerelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Radiation therapy for early-stage breast cancer is typically delivered in a hypofractionated regimen to the whole breast followed by a tumor bed boost. This results in a treatment course of approximately 4 weeks. In this study, the tumor bed boost was delivered in a single fraction as part of a safety and feasibility study for FDA clearance of the device. Methods and Materials: Eligible women with early-stage breast cancer underwent lumpectomy followed by radiation therapy. Patients underwent breast immobilization using a system specific to the GammaPod followed by CT simulation, boost treatment planning, and boost treatment delivery all in a single treatment day. Patients then started whole-breast radiation therapy within 1 week of the boost treatment. Patients and treatments were assessed for safety and feasibility. Acute toxicities were recorded. Results: A single-fraction boost of 8 Gy was delivered to the tumor bed before a course of whole-breast radiation. The GammaPod treatment was successfully delivered to 14 of 17 enrolled patients. Acute toxicities from all radiation therapy, inclusive of the boost and whole-breast radiation, were limited to grade 1 events. Conclusions: The GammaPod device successfully delivered a single-fraction boost treatment to the tumor bed with no change in expected acute toxicities. The results of this study led to FDA clearance of the device through the Investigational Device Exemption process at the FDA. The GammaPod is in clinical use at 4e institutions nationally and internationally, with additional sites pending in 2023.

Identifiers

PMID38778822
PMCPMC11110030

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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.