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Patterns of failure after iodine-125 seed implantation for prostate cancer.
Lamb, David S; Greig, Lynne; Russell, Grant L; Nacey, John N; Broome, Kim; Studd, Rod; Delahunt, Brett; Iupati, Douglas; Jain, Mohua; Rooney, Colin; Murray, Judy; Lamb, Peter J; Bethwaite, Peter B.
Afiliación
  • Lamb DS; Prostate Cancer Trials Unit, Department of Pathology and Molecular Medicine, University of Otago, Wellington, New Zealand; Radiation Oncology, Southern Cross Hospital, Wellington, New Zealand. Electronic address: David.Lamb@otago.ac.nz.
  • Greig L; Medical Physics, Southern Cross Hospital, Wellington, New Zealand.
  • Russell GL; Urology, Southern Cross Hospital, Wellington, New Zealand.
  • Nacey JN; Prostate Cancer Trials Unit, Department of Pathology and Molecular Medicine, University of Otago, Wellington, New Zealand; Urology, Southern Cross Hospital, Wellington, New Zealand.
  • Broome K; Omahu Urology Clinic, Hawkes Bay, New Zealand.
  • Studd R; Urology, Southern Cross Hospital, Wellington, New Zealand.
  • Delahunt B; Prostate Cancer Trials Unit, Department of Pathology and Molecular Medicine, University of Otago, Wellington, New Zealand.
  • Iupati D; Radiation Oncology, Southern Cross Hospital, Wellington, New Zealand.
  • Jain M; Anesthetics, Southern Cross Hospital, Wellington, New Zealand.
  • Rooney C; Medical Physics, Southern Cross Hospital, Wellington, New Zealand.
  • Murray J; Prostate Cancer Trials Unit, Department of Pathology and Molecular Medicine, University of Otago, Wellington, New Zealand.
  • Lamb PJ; Prostate Cancer Trials Unit, Department of Pathology and Molecular Medicine, University of Otago, Wellington, New Zealand.
  • Bethwaite PB; Prostate Cancer Trials Unit, Department of Pathology and Molecular Medicine, University of Otago, Wellington, New Zealand.
Radiother Oncol ; 112(1): 68-71, 2014 Jul.
Article en En | MEDLINE | ID: mdl-25082097
ABSTRACT

PURPOSE:

To determine the site of relapse when biochemical failure (BF) occurs after iodine-125 seed implantation for prostate cancer. MATERIALS AND

METHODS:

From 2001-2009, 500 men underwent implantation in Wellington, New Zealand. Men who sustained BF were placed on relapse guidelines that delayed restaging and intervention until the prostate-specific antigen (PSA) was ⩾20 ng/mL.

RESULTS:

Most implants (86%) had a prostate D90 of ⩾90%, and multivariate analysis showed that this parameter was not a variable that affected the risk of BF. Of 21 BFs that occurred, the site of failure was discovered to be local in one case and distant in nine cases. Restaging failed to identify the site of relapse in two cases. In nine cases the trigger for restaging had not been reached.

CONCLUSIONS:

If post-implant dosimetry is generally within the optimal range, distant rather than local failure appears to be the main cause of BF. Hormone treatment is therefore the most commonly indicated secondary treatment intervention (STI). Delaying the start of STI prevents the unnecessary treatment of men who undergo PSA 'bounce' and have PSA dynamics initially mimicking those of BF.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Braquiterapia / Antígeno Prostático Específico / Radioisótopos de Yodo / Recurrencia Local de Neoplasia Tipo de estudio: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Humans / Male / Middle aged Idioma: En Revista: Radiother Oncol Año: 2014 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias de la Próstata / Braquiterapia / Antígeno Prostático Específico / Radioisótopos de Yodo / Recurrencia Local de Neoplasia Tipo de estudio: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Humans / Male / Middle aged Idioma: En Revista: Radiother Oncol Año: 2014 Tipo del documento: Article