Feasibility of transrectal and transperineal fiducial marker placement for prostate cancer before proton therapy.


Journal

Japanese journal of clinical oncology
ISSN: 1465-3621
Titre abrégé: Jpn J Clin Oncol
Pays: England
ID NLM: 0313225

Informations de publication

Date de publication:
08 Feb 2021
Historique:
received: 23 04 2020
accepted: 25 08 2020
pubmed: 9 10 2020
medline: 25 2 2021
entrez: 8 10 2020
Statut: ppublish

Résumé

To compare the feasibility of transrectal and transperineal fiducial marker placement for prostate cancer before proton therapy. From 2013 to 2015, the first 40 prostate cancer patients that were scheduled for proton therapy underwent transrectal fiducial marker placement, and the next 40 patients underwent transperineal fiducial marker placement (the first series). Technical and clinical success and pain scores were evaluated. In the second series (n = 280), the transrectal or transperineal approach was selected depending on the presence/absence of comorbidities, such as blood coagulation abnormalities. Seven patients refused to undergo the procedure. Thus, the total number of patients across both series was 353 (262 and 91 underwent the transrectal and transperineal approach, respectively). Technical and clinical success, complications, marker migration and the distance between the two markers were evaluated. In the first series, the technical and clinical success rates were 100% in both groups. The transrectal group exhibited lower pain scores than the transperineal group. The overall technical success rates of the transrectal and transperineal groups were 100% (262/262) and 99% (90/91), respectively (P > 0.05). The overall clinical success rate was 100% in both groups, and there were no major complications in either group. The migration rates of the two groups did not differ significantly. The mean distance between the two markers was 25.6 ± 7.1 mm (mean ± standard deviation) in the transrectal group and 31.9 ± 5.2 mm in the transperineal group (P < 0.05). Both the transrectal and transperineal fiducial marker placement methods are feasible and safe.

Sections du résumé

BACKGROUND BACKGROUND
To compare the feasibility of transrectal and transperineal fiducial marker placement for prostate cancer before proton therapy.
MATERIALS AND METHODS METHODS
From 2013 to 2015, the first 40 prostate cancer patients that were scheduled for proton therapy underwent transrectal fiducial marker placement, and the next 40 patients underwent transperineal fiducial marker placement (the first series). Technical and clinical success and pain scores were evaluated. In the second series (n = 280), the transrectal or transperineal approach was selected depending on the presence/absence of comorbidities, such as blood coagulation abnormalities. Seven patients refused to undergo the procedure. Thus, the total number of patients across both series was 353 (262 and 91 underwent the transrectal and transperineal approach, respectively). Technical and clinical success, complications, marker migration and the distance between the two markers were evaluated.
RESULTS RESULTS
In the first series, the technical and clinical success rates were 100% in both groups. The transrectal group exhibited lower pain scores than the transperineal group. The overall technical success rates of the transrectal and transperineal groups were 100% (262/262) and 99% (90/91), respectively (P > 0.05). The overall clinical success rate was 100% in both groups, and there were no major complications in either group. The migration rates of the two groups did not differ significantly. The mean distance between the two markers was 25.6 ± 7.1 mm (mean ± standard deviation) in the transrectal group and 31.9 ± 5.2 mm in the transperineal group (P < 0.05).
CONCLUSION CONCLUSIONS
Both the transrectal and transperineal fiducial marker placement methods are feasible and safe.

Identifiants

pubmed: 33029639
pii: 5919201
doi: 10.1093/jjco/hyaa172
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

258-263

Informations de copyright

© Crown copyright 2020.

Auteurs

Kengo Ohta (K)

Department of Radiology, Nagoya City University Graduate School of Medical Sciences, Nagoya.

Hiroyuki Ogino (H)

Department of Radiation Oncology, Nagoya Proton Therapy Center, Nagoya City West Medical Center, Nagoya.

Hiromitsu Iwata (H)

Department of Radiation Oncology, Nagoya Proton Therapy Center, Nagoya City West Medical Center, Nagoya.

Shingo Hashimoto (S)

Department of Radiation Oncology, Nagoya Proton Therapy Center, Nagoya City West Medical Center, Nagoya.

Yukiko Hattori (Y)

Department of Radiation Oncology, Nagoya Proton Therapy Center, Nagoya City West Medical Center, Nagoya.

Koichiro Nakajima (K)

Department of Radiation Oncology, Nagoya Proton Therapy Center, Nagoya City West Medical Center, Nagoya.

Maho Yamada (M)

Department of Radiation Oncology, Nagoya City West Medical Center, Nagoya, Japan.

Masashi Shimohira (M)

Department of Radiology, Nagoya City University Graduate School of Medical Sciences, Nagoya.

Jun-Etsu Mizoe (JE)

Department of Radiation Oncology, Nagoya Proton Therapy Center, Nagoya City West Medical Center, Nagoya.

Yuta Shibamoto (Y)

Department of Radiology, Nagoya City University Graduate School of Medical Sciences, Nagoya.

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