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SPCG-15 : a prospective randomized study comparing primary radical prostatectomy and primary radiotherapy plus androgen deprivation therapy for locally advanced prostate cancer

Stranne, Johan, 1970 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för urologi,Institute of Clinical Sciences, Department of Urology
Brasso, K. (author)
Rigshosp Copenhagen, Copenhagen Prostate Canc Ctr, Copenhagen, Denmark; Rigshosp Copenhagen, Dept Urol, Copenhagen, Denmark
Brennhovd, B. (author)
Oslo Univ Hosp HF, Dept Urooncol, Radiumhosp, Oslo, Norway
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Johansson, Eva (author)
Uppsala universitet,Urologkirurgi
Jäderling, F. (author)
Karolinska Institutet
Kouri, M. (author)
Helsinki Univ Hosp, Dept Oncol, Helsinki, Finland
Lilleby, W. (author)
Oslo Univ Hosp HF, Dept Urooncol, Radiumhosp, Oslo, Norway
Petersen, P. Meidahl (author)
Copenhagen Univ Hosp, Dept Oncol, Finsen Ctr, Copenhagen, Denmark
Mirtti, T. (author)
Univ Helsinki, Inst Mol Med Finland FIMM, Helsinki, Finland
Pettersson, A. (author)
Karolinska Institutet
Rannikko, A. (author)
Helsinki Univ Hosp, Dept Urol, Helsinki, Finland
Thellenberg, C. (author)
Norrlands Univ Hosp, Cancerctr, Umeå, Sweden
Akre, O. (author)
Karolinska Institutet
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 (creator_code:org_t)
2018-12-26
2018
English.
In: Scandinavian journal of urology. - : Medical Journals Sweden AB. - 2168-1805 .- 2168-1813. ; 52:5-6, s. 313-320
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Objective: To describe study design and procedures for a prospective randomized trial investigating whether radical prostatectomy (RP) ± radiation improves cause-specific survival in comparison with primary radiation treatment (RT) and androgen deprivation treatment (ADT) in patients with locally advanced prostate cancer (LAPC).Materials and methods: SPCG-15 is a prospective, multi-centre, open randomized phase III trial. Patients are randomized to either standard (RT + ADT) or experimental (RP with extended pelvic lymph-node dissection and with addition of adjuvant or salvage RT and/or ADT if deemed necessary) treatment. Each centre follows guidelines regarding the timing and dosing of postoperative RT and adjuvant treatment such as ADT The primary endpoint is cause-specific survival. Secondary endpoints include metastasis-free and overall survival, quality-of-life, functional outcomes and health-services requirements. Each subject will be followed up for a minimum of 10 years.Results: Twenty-three centres in Denmark, Finland, Norway and Sweden, well established in performing RP and RT for prostate cancer participated. Each country’s sites were coordinated by national coordinating investigators and sub-investigators for urology and oncology. Almost 400 men have been randomized of the stipulated 1200, with an increasing rate of accrual.Conclusions: The SPCG-15 trial aims to compare the two curatively intended techniques supplying new knowledge to support future decisions in treatment strategies for patients with LAPC The Scandinavian healthcare context is well suited for performing multi-centre long-term prospective randomized clinical trials. Similar care protocols and a history of entirely tax-funded healthcare facilitate joint trials.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Urologi och njurmedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Urology and Nephrology (hsv//eng)

Keyword

Locally advanced prostate cancer
radical prostatectomy
radiotherapy
androgen deprivation therapy

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