Evidence map›Paper›PMID 37996094›Full record

ArticleJournal of radiation research2024

Real-time tumor-tracking radiotherapy with SyncTraX for primary liver tumors requiring isocenter shift†.

Yusuke Uchinami, Naoki Miyamoto, Daisuke Abo, Ryo Morita, Koji Ogawa, Tatsuhiko Kakisaka, Ryusuke Suzuki, Tomohiko Miyazaki, Hiroshi Taguchi, Norio Katoh and 1 more

Abstract read
In one paragraph

Article in Journal of radiation research, 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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0cells of the map it votes in
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

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

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5 · Who and what money

Authors and funding

11 authors.

Yusuke UchinamiDepartment of Radiation Oncology, Hokkaido University Faculty of Medicine and Graduate School of Medicine, North 15 West 7, Kita-ku, Sapporo 060-8638, Japan.
Naoki MiyamotoDepartment of Medical Physics, Hokkaido University Hospital, North 14 West 5, Kita-ku, Sapporo 060-8648, Japan.
Daisuke AboDepartment of Diagnostic and Interventional Radiology, Hokkaido University Hospital, North 14 West 5, Kita-ku, Sapporo 060-8648, Japan.
Ryo MoritaDepartment of Diagnostic and Interventional Radiology, Hokkaido University Hospital, North 14 West 5, Kita-ku, Sapporo 060-8648, Japan.
Koji OgawaDepartment of Gastroenterology and Hepatology, Hokkaido University Faculty of Medicine, North 15 West 7, Kita-ku, Sapporo 060-8638, Japan.
Tatsuhiko KakisakaDepartment of Gastroenterological Surgery, Hokkaido University Faculty of Medicine, North 15 West 7, Kita-ku, Sapporo, Hokkaido 060-8638, Japan.
Ryusuke SuzukiDepartment of Medical Physics, Hokkaido University Hospital, North 14 West 5, Kita-ku, Sapporo 060-8648, Japan.
Tomohiko MiyazakiDepartment of Radiation Oncology, Hokkaido University Hospital, North 14 West 5, Kita-ku, Sapporo 060-8648, Japan.
Hiroshi TaguchiDepartment of Radiation Oncology, Hokkaido University Hospital, North 14 West 5, Kita-ku, Sapporo 060-8648, Japan.
Norio KatohDepartment of Radiation Oncology, Hokkaido University Faculty of Medicine and Graduate School of Medicine, North 15 West 7, Kita-ku, Sapporo 060-8638, Japan.
Hidefumi AoyamaDepartment of Radiation Oncology, Hokkaido University Faculty of Medicine and Graduate School of Medicine, North 15 West 7, Kita-ku, Sapporo 060-8638, Japan.

Funding

Grant-in-Aid for Research on Radiation Oncology 23 K14857Japan Society for the Promotion of Science KAKENHI
6 · The paper itself

Abstract

The SyncTraX series enables real-time tumor-tracking radiotherapy through the real-time recognition of a fiducial marker using fluoroscopic images. In this system, the isocenter should be located within approximately 5-7.5 cm from the marker, depending on the version, owing to the limited field of view. If the marker is placed away from the tumor, the isocenter should be shifted toward the marker. This study aimed to investigate stereotactic body radiotherapy (SBRT) outcomes of primary liver tumors treated with SyncTraX in cases where the isocenter was shifted marginally or outside the planning target volume (PTV). Twelve patients with 13 liver tumors were included in the analysis. Their isocenter was shifted toward the marker and was placed marginally or outside the PTV. The prescribed doses were generally 40 Gy in four fractions or 48 Gy in eight fractions. The overall survival (OS) and local control (LC) rates were calculated using the Kaplan-Meier method. All patients completed the scheduled SBRT. The median distance between the fiducial marker and PTV centroid was 56.0 (interquartile range [IQR]: 52.7-66.7) mm. By shifting the isocenter toward the marker, the median distance between the marker and isocenter decreased to 34.0 (IQR: 33.4-39.7) mm. With a median follow-up period of 25.3 (range: 6.9-70.0) months, the 2-year OS and LC rates were 100.0% (95% confidence interval: 100-100). An isocenter shift makes SBRT with SyncTraX feasible in cases where the fiducial marker is distant from the tumor.

Indexed as

Liver NeoplasmsRadiosurgeryRadiotherapy, Intensity-ModulatedHumansRadiotherapy DosageRadiotherapy Planning, Computer-AssistedRetrospective Studiesprimary liver tumorsreal-time tumor-tracking radiotherapySBRTSyncTraXSyncTraX FX4

Identifiers

PMID37996094
PMCPMC10803168

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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.