Reduction in acute morbidity using hypofractionated intensity-modulated radiation therapy assisted with a fluoroscopic real-time tumor-tracking system for prostate cancer: preliminary results of a phase I/II study.

Purpose: The positioning of the prostate is improved with the use of the fluoroscopic real-time tumor-tracking radiation therapy system for prostate cancer. The acute radiation reaction and preliminary tumor response of prostate cancer to hypofractionated intensity-modulated radiation therapy assist...

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Publicado en:Cancer Journal Vol. 9; no. 4; pp. 268 - 277
Autores principales: Kitamura K, Shirato H, Shinohara N, Harabayashi T, Onimaru R, Fujita K, Shimizu S, Nonomura K, Koyanagi T, Miyasaka K, Kitamura, Kei, Shirato, Hiroki, Shinohara, Nobuo, Harabayashi, Toru, Onimaru, Rikiya, Fujita, Katsuhisa, Shimizu, Shinichi, Nonomura, Katsuya, Koyanagi, Tomohiko, Miyasaka, Kazuo
Formato: clinical trial diagnostic images research tables/charts Journal Article
Publicado: Lippincott Williams & Wilkins Jul/Aug2003
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Jul/Aug2003
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      pub: Lippincott Williams & Wilkins
      place: Baltimore, Maryland
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        106751503
        106751503
        NLM12967137
        2004111820
        10.1097/00130404-200307000-00009
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        106751503
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        atl: Reduction in acute morbidity using hypofractionated intensity-modulated radiation therapy assisted with a fluoroscopic real-time tumor-tracking system for prostate cancer: preliminary results of a phase I/II study.
      aug:
        au:
          Kitamura K
          Shirato H
          Shinohara N
          Harabayashi T
          Onimaru R
          Fujita K
          Shimizu S
          Nonomura K
          Koyanagi T
          Miyasaka K
          Kitamura, Kei
          Shirato, Hiroki
          Shinohara, Nobuo
          Harabayashi, Toru
          Onimaru, Rikiya
          Fujita, Katsuhisa
          Shimizu, Shinichi
          Nonomura, Katsuya
          Koyanagi, Tomohiko
          Miyasaka, Kazuo
        affil: Department of Radiology, Hokkaido University School of Medicine, Sapporo, Japan
      sug:
        subj:
          Prostatic Neoplasms Radiotherapy
          Radiotherapy Methods
          Dose-Response Relationship, Radiation
          Radiotherapy Adverse Effects
          Radiation Injuries Etiology
          Therapy, Computer Assisted
          Treatment Outcomes
          Radiation Dosage
          Fluoroscopy
          Clinical Trials
          Chi Square Test
          Human
      ab: Purpose: The positioning of the prostate is improved with the use of the fluoroscopic real-time tumor-tracking radiation therapy system for prostate cancer. The acute radiation reaction and preliminary tumor response of prostate cancer to hypofractionated intensity-modulated radiation therapy assisted with real-time tumor-tracking radiation therapy were investigated in this study.Methods: Patients were classified into prognostic risk groups on the basis of the presence of the pretreatment prostate-specific antigen, clinical stage, and histologic differentiation. Neoadjuvant hormonal therapy was administered to patients in the high-risk group for 6 months before radiation therapy commenced. The intensity-modulated radiation therapy employed a segmental multileaf collimator, which generated a field made up of two or more shaped subfields using forward planning. Real-time tumor-tracking radiation therapy was used for the precise positioning of the prostate to minimize geometric uncertainties, while the dose was escalated in increments of 5 Gy from 65 Gy using a daily dose of 2.5 Gy (65 Gy/2.5 Gy), following the dose-escalation rules. Acute and late gastrointestinal and genitourinary morbidities due to radiation therapy were scored according to the toxicity criteria of Radiation Therapy Oncology Group/European Organization for Research and Treatment of Cancer.Results: Thirty-one patients were enrolled in this study between 1998 and 2001. Eighteen patients were classified as being members of the high-risk group. Total dose was escalated, with 65 Gy/2.5 Gy being administered to 12 patients and 70 Gy/2.5 Gy to 19 patients. The median follow-up period was 37 months (range, 30-43 months), and 19 months (range, 10-27 months), for the 65-Gy and 70-Gy arms, respectively. Patients experienced no acute toxicity and grade 1 late gastrointestinal toxicity (8.3%) in the 65-Gy/2.5-Gy arm. Patients in the 70-Gy/2.5-Gy arm experienced grade 1 acute gastrointestinal toxicity (5.3%) and grade 1 and 2 acute genitourinarytoxicities (15.8%). No patients experienced dose-limiting toxicity (defined as a grade 3 or higher acute toxicity) or a grade 2 or higher late complication in this study period. One and two prostate-specific antigen relapses were observed in the 65-Gy and 70-Gy arms, respectively.Conclusion: Up to 70 Gy/2.5 Gy, equivalent to 80 Gy with a daily dose of 2.0 Gy, assuming alpha/beta ratio of 1.5, intensity-modulated radiation therapy assisted with real-time tumor-tracking radiation therapy was administered safely with a reasonable biochemical control rate. A further dose-escalation study using this system is justifiable.
      pubtype: Academic Journal
      doctype:
        clinical trial
        diagnostic images
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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