Prostate-specific antigen kinetics following external-beam radiotherapy and temporary (Ir-192) or permanent (I-125) brachytherapy for prostate cancer

The aim of the study was the evaluation of PSA kinetics after different radiotherapy methods. Two-hundred and ninety five patients received external-beam radiotherapy (EBRT; 70.2 Gy; n = 135), Ir-192 brachytherapy as a boost to EBRT (HDR-BT; 18 Gy + 50.4 Gy; n = 66) or I-125 brachytherapy (LDR-BT; 1...

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Published inRadiotherapy and oncology Vol. 96; no. 1; pp. 25 - 29
Main Authors Pinkawa, Michael, Piroth, Marc D., Holy, Richard, Fischedick, Karin, Schaar, Sandra, Borchers, Holger, Heidenreich, Axel, Eble, Michael J.
Format Journal Article
LanguageEnglish
Published Ireland Elsevier Ireland Ltd 01.07.2010
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ISSN0167-8140
1879-0887
1879-0887
DOI10.1016/j.radonc.2010.02.010

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Abstract The aim of the study was the evaluation of PSA kinetics after different radiotherapy methods. Two-hundred and ninety five patients received external-beam radiotherapy (EBRT; 70.2 Gy; n = 135), Ir-192 brachytherapy as a boost to EBRT (HDR-BT; 18 Gy + 50.4 Gy; n = 66) or I-125 brachytherapy (LDR-BT; 145 Gy; n = 94) as monotherapy. “PSA bounce” was defined as a PSA rise of ⩾0.2 ng/ml followed by spontaneous return to prebounce level or lower, biochemical failure as “nadir + 2 ng/ml”. Patients without biochemical failure reached a lower nadir after brachytherapy (median ⩽0.05 ng/ml after LDR- and HDR-BT without NHT) in comparison to EBRT (0.55 ng/ml without NHT; p < 0.01). Not a single patient without NHT and a nadir <0.1 ng/ml failed biochemically (0% vs. 45% with a nadir ⩾0.1 ng/ml; p < 0.01). PSA bounces were found predominantly in the LDR-BT group (42% vs. 23%/20% after HDR-BT/EBRT; p < 0.01). In a multivariate Cox regression analysis, LDR-BT and HDR-BT were associated with a significantly lower biochemical failure rate in comparison to EBRT. PSA kinetics differ significantly following different radiotherapy methods. A lower nadir and a higher biochemical control rate suggest a higher radiobiological efficiency of brachytherapy in comparison to EBRT (with a dose of 70.2 Gy).
AbstractList The aim of the study was the evaluation of PSA kinetics after different radiotherapy methods. Two-hundred and ninety five patients received external-beam radiotherapy (EBRT; 70.2 Gy; n = 135), Ir-192 brachytherapy as a boost to EBRT (HDR-BT; 18 Gy + 50.4 Gy; n = 66) or I-125 brachytherapy (LDR-BT; 145 Gy; n = 94) as monotherapy. “PSA bounce” was defined as a PSA rise of ⩾0.2 ng/ml followed by spontaneous return to prebounce level or lower, biochemical failure as “nadir + 2 ng/ml”. Patients without biochemical failure reached a lower nadir after brachytherapy (median ⩽0.05 ng/ml after LDR- and HDR-BT without NHT) in comparison to EBRT (0.55 ng/ml without NHT; p < 0.01). Not a single patient without NHT and a nadir <0.1 ng/ml failed biochemically (0% vs. 45% with a nadir ⩾0.1 ng/ml; p < 0.01). PSA bounces were found predominantly in the LDR-BT group (42% vs. 23%/20% after HDR-BT/EBRT; p < 0.01). In a multivariate Cox regression analysis, LDR-BT and HDR-BT were associated with a significantly lower biochemical failure rate in comparison to EBRT. PSA kinetics differ significantly following different radiotherapy methods. A lower nadir and a higher biochemical control rate suggest a higher radiobiological efficiency of brachytherapy in comparison to EBRT (with a dose of 70.2 Gy).
The aim of the study was the evaluation of PSA kinetics after different radiotherapy methods. Two-hundred and ninety five patients received external-beam radiotherapy (EBRT; 70.2 Gy; n=135), Ir-192 brachytherapy as a boost to EBRT (HDR-BT; 18 Gy+50.4 Gy; n=66) or I-125 brachytherapy (LDR-BT; 145 Gy; n=94) as monotherapy. "PSA bounce" was defined as a PSA rise of > or = 0.2 ng/ml followed by spontaneous return to prebounce level or lower, biochemical failure as "nadir+2 ng/ml". Patients without biochemical failure reached a lower nadir after brachytherapy (median < or = 0.05 ng/ml after LDR- and HDR-BT without NHT) in comparison to EBRT (0.55 ng/ml without NHT; p<0.01). Not a single patient without NHT and a nadir <0.1 ng/ml failed biochemically (0% vs. 45% with a nadir > or = 0.1 ng/ml; p<0.01). PSA bounces were found predominantly in the LDR-BT group (42% vs. 23%/20% after HDR-BT/EBRT; p<0.01). In a multivariate Cox regression analysis, LDR-BT and HDR-BT were associated with a significantly lower biochemical failure rate in comparison to EBRT. PSA kinetics differ significantly following different radiotherapy methods. A lower nadir and a higher biochemical control rate suggest a higher radiobiological efficiency of brachytherapy in comparison to EBRT (with a dose of 70.2 Gy).
AbstractBackground and purposeThe aim of the study was the evaluation of PSA kinetics after different radiotherapy methods. Materials and methodsTwo-hundred and ninety five patients received external-beam radiotherapy (EBRT; 70.2 Gy; n= 135), Ir-192 brachytherapy as a boost to EBRT (HDR-BT; 18 Gy + 50.4 Gy; n= 66) or I-125 brachytherapy (LDR-BT; 145 Gy; n= 94) as monotherapy. “PSA bounce” was defined as a PSA rise of ⩾0.2 ng/ml followed by spontaneous return to prebounce level or lower, biochemical failure as “nadir + 2 ng/ml”. ResultsPatients without biochemical failure reached a lower nadir after brachytherapy (median ⩽0.05 ng/ml after LDR- and HDR-BT without NHT) in comparison to EBRT (0.55 ng/ml without NHT; p< 0.01). Not a single patient without NHT and a nadir <0.1 ng/ml failed biochemically (0% vs. 45% with a nadir ⩾0.1 ng/ml; p< 0.01). PSA bounces were found predominantly in the LDR-BT group (42% vs. 23%/20% after HDR-BT/EBRT; p< 0.01). In a multivariate Cox regression analysis, LDR-BT and HDR-BT were associated with a significantly lower biochemical failure rate in comparison to EBRT. ConclusionsPSA kinetics differ significantly following different radiotherapy methods. A lower nadir and a higher biochemical control rate suggest a higher radiobiological efficiency of brachytherapy in comparison to EBRT (with a dose of 70.2 Gy).
The aim of the study was the evaluation of PSA kinetics after different radiotherapy methods.BACKGROUND AND PURPOSEThe aim of the study was the evaluation of PSA kinetics after different radiotherapy methods.Two-hundred and ninety five patients received external-beam radiotherapy (EBRT; 70.2 Gy; n=135), Ir-192 brachytherapy as a boost to EBRT (HDR-BT; 18 Gy+50.4 Gy; n=66) or I-125 brachytherapy (LDR-BT; 145 Gy; n=94) as monotherapy. "PSA bounce" was defined as a PSA rise of > or = 0.2 ng/ml followed by spontaneous return to prebounce level or lower, biochemical failure as "nadir+2 ng/ml".MATERIALS AND METHODSTwo-hundred and ninety five patients received external-beam radiotherapy (EBRT; 70.2 Gy; n=135), Ir-192 brachytherapy as a boost to EBRT (HDR-BT; 18 Gy+50.4 Gy; n=66) or I-125 brachytherapy (LDR-BT; 145 Gy; n=94) as monotherapy. "PSA bounce" was defined as a PSA rise of > or = 0.2 ng/ml followed by spontaneous return to prebounce level or lower, biochemical failure as "nadir+2 ng/ml".Patients without biochemical failure reached a lower nadir after brachytherapy (median < or = 0.05 ng/ml after LDR- and HDR-BT without NHT) in comparison to EBRT (0.55 ng/ml without NHT; p<0.01). Not a single patient without NHT and a nadir <0.1 ng/ml failed biochemically (0% vs. 45% with a nadir > or = 0.1 ng/ml; p<0.01). PSA bounces were found predominantly in the LDR-BT group (42% vs. 23%/20% after HDR-BT/EBRT; p<0.01). In a multivariate Cox regression analysis, LDR-BT and HDR-BT were associated with a significantly lower biochemical failure rate in comparison to EBRT.RESULTSPatients without biochemical failure reached a lower nadir after brachytherapy (median < or = 0.05 ng/ml after LDR- and HDR-BT without NHT) in comparison to EBRT (0.55 ng/ml without NHT; p<0.01). Not a single patient without NHT and a nadir <0.1 ng/ml failed biochemically (0% vs. 45% with a nadir > or = 0.1 ng/ml; p<0.01). PSA bounces were found predominantly in the LDR-BT group (42% vs. 23%/20% after HDR-BT/EBRT; p<0.01). In a multivariate Cox regression analysis, LDR-BT and HDR-BT were associated with a significantly lower biochemical failure rate in comparison to EBRT.PSA kinetics differ significantly following different radiotherapy methods. A lower nadir and a higher biochemical control rate suggest a higher radiobiological efficiency of brachytherapy in comparison to EBRT (with a dose of 70.2 Gy).CONCLUSIONSPSA kinetics differ significantly following different radiotherapy methods. A lower nadir and a higher biochemical control rate suggest a higher radiobiological efficiency of brachytherapy in comparison to EBRT (with a dose of 70.2 Gy).
Author Fischedick, Karin
Borchers, Holger
Piroth, Marc D.
Holy, Richard
Schaar, Sandra
Eble, Michael J.
Heidenreich, Axel
Pinkawa, Michael
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/20231039$$D View this record in MEDLINE/PubMed
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Issue 1
Keywords Hormone therapy
Prostate-specific antigen
I-125
Brachytherapy
Ir-192
Radiotherapy
Prostate cancer
Language English
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Snippet The aim of the study was the evaluation of PSA kinetics after different radiotherapy methods. Two-hundred and ninety five patients received external-beam...
AbstractBackground and purposeThe aim of the study was the evaluation of PSA kinetics after different radiotherapy methods. Materials and methodsTwo-hundred...
The aim of the study was the evaluation of PSA kinetics after different radiotherapy methods.BACKGROUND AND PURPOSEThe aim of the study was the evaluation of...
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StartPage 25
SubjectTerms Adenocarcinoma - blood
Adenocarcinoma - mortality
Adenocarcinoma - pathology
Adenocarcinoma - radiotherapy
Aged
Aged, 80 and over
Brachytherapy
Brachytherapy - methods
Chi-Square Distribution
Cohort Studies
Confidence Intervals
Dose-Response Relationship, Radiation
Follow-Up Studies
Hematology, Oncology, and Palliative Medicine
Hormone therapy
Humans
I-125
Ir-192
Kaplan-Meier Estimate
Male
Middle Aged
Neoplasm Staging
Proportional Hazards Models
Prostate cancer
Prostate-specific antigen
Prostate-Specific Antigen - pharmacokinetics
Prostate-Specific Antigen - radiation effects
Prostatic Neoplasms - blood
Prostatic Neoplasms - mortality
Prostatic Neoplasms - pathology
Prostatic Neoplasms - radiotherapy
Radiotherapy
Radiotherapy Dosage
Radiotherapy, High-Energy - methods
Risk Assessment
Survival Rate
Time Factors
Treatment Outcome
Title Prostate-specific antigen kinetics following external-beam radiotherapy and temporary (Ir-192) or permanent (I-125) brachytherapy for prostate cancer
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0167814010001039
https://www.clinicalkey.es/playcontent/1-s2.0-S0167814010001039
https://dx.doi.org/10.1016/j.radonc.2010.02.010
https://www.ncbi.nlm.nih.gov/pubmed/20231039
https://www.proquest.com/docview/733655595
Volume 96
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