Evidence map›Paper›PMID 36157159›Full record

ArticleWorld journal of clinical oncology2022

Assessing radiation dose for postoperative radiotherapy in prostate cancer: Real world data.

Asunción Hervás-Morón, Jose Domínguez-Rullán, Victor Duque Santana, Mireia Valero, Carmen Vallejo, Sonsoles Sancho, Juan David García Fuentes, Fernando López-Campos, Miguel Cámara Gallego

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Article in World journal of clinical oncology, 2022. 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Asunción Hervás-MorónDepartment of Radiation Oncology, Hospital Universitario Ramón Y Cajal, Madrid 28034, Spain.
Jose Domínguez-RullánDepartment of Radiation Oncology, Hospital Universitario Ramón Y Cajal, Madrid 28034, Spain.
Victor Duque SantanaDepartment of Radiation Oncology, Hospital Universitario Ramón Y Cajal, Madrid 28034, Spain.
Mireia ValeroDepartment of Radiation Oncology, Hospital Universitario Ramón Y Cajal, Madrid 28034, Spain.
Carmen VallejoDepartment of Radiation Oncology, Hospital Universitario Ramón Y Cajal, Madrid 28034, Spain.
Sonsoles SanchoDepartment of Radiation Oncology, Hospital Universitario Ramón Y Cajal, Madrid 28034, Spain.
Juan David García FuentesDepartment of Medical Physics, Hospital Universitario Ramón Y Cajal, Madrid 28034, Spain.
Fernando López-CamposDepartment of Radiation Oncology, Hospital Universitario Ramón Y Cajal, Madrid 28034, Spain. fernando_lopez_campos@hotmail.com.
Miguel Cámara GallegoDepartment of Medical Physics, Hospital Universitario Ramón Y Cajal, Madrid 28034, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundApproximately 30% of patients with localized prostate cancer (PCa) who undergo radical prostatectomy will develop biochemical recurrence. In these patients, the only potentially curative treatment is postoperative radiotherapy (PORT) with or without hormone therapy. However, the optimal radiotherapy dose is unknown due to the limited data available.

aimTo determine whether the postoperative radiotherapy dose influences biochemical failure-free survival (BFFS) in patients with PCa.

methodsRetrospective analysis of patients who underwent radical prostatectomy for PCa followed by PORT-either adjuvant radiotherapy (ART) or salvage radiotherapy (SRT)-between April 2002 and July 2015. From 2002 to 2010, the prescribed radiation dose to the surgical bed was 66-70 Gy in fractions of 2 Gy; from 2010 until July 2015, the prescribed dose was 70-72 Gy. Patients were grouped into three categories according to the total dose administered: 66-68 Gy, 70 Gy, and 72 Gy. The primary endpoint was BFFS, defined as the post-radiotherapy prostate-specific antigen (PSA) nadir + 0.2 ng/mL. Secondary endpoints were overall survival (OS), cancer-specific survival (CSS), and metastasis-free survival (MFS; based on conventional imaging tests). Treatment-related genitourinary (GU) and gastrointestinal (GI) toxicity was evaluated according to Radiation Therapy Oncology Group/European Organization for Research and Treatment of Cancer criteria. Finally, we aimed to identify potential prognostic factors. BFFS, OS, CSS, and MFS were calculated with the Kaplan-Meier method and the log-rank test. Univariate and multivariate Cox regression models were performed to explore between-group differences in survival outcome measures.

resultsA total of 301 consecutive patients were included. Of these, 93 (33.6%) received ART and 186 (66.4%) SRT; 22 patients were excluded due to residual macroscopic disease or local recurrence in the surgical bed. In this subgroup (

conclusionThe findings of this retrospective study suggest that postoperative radiotherapy dose intensification in PCa is not superior to conventional radiotherapy treatment.

Indexed as

Biochemical relapse free survivalDose intensifiedPostoperative radiotherapyProstate cancerRadiation dose

Identifiers

PMID36157159
PMCPMC9346429

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