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Chemotherapy vs tamoxifen in platinum-resistant ovarian cancer: a phase III, randomised, multicentre trial (Ovaresist)

Lindemann, Kristina (author)
Oslo University Hospital, Norway; University of Sydney, Australia; Westmead Hospital, Australia
Gibbs, Emma (author)
University of Sydney, Australia
Åvall-Lundqvist, Elisabeth, 1957- (author)
Karolinska Institutet,Linköpings universitet,Avdelningen för Kirurgi, Ortopedi och Onkologi,Medicinska fakulteten,Region Östergötland, Onkologiska kliniken US,Karolinska Institute, Sweden
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dePont Christensen, Rene (author)
University of Southern Denmark, Denmark
Woie, Kathrine (author)
Haukeland Hospital, Norway
Kalling, Marten (author)
Skåne University Hospital, Sweden
Auranen, Annika (author)
Tampere University Hospital, Finland
Grenman, Seija (author)
Turku University Hospital, Finland; University of Turku, Finland
Hoegberg, Thomas (author)
Skåne University Hospital Lund, Sweden
Rosenberg, Per (author)
Linköpings universitet,Avdelningen för kliniska vetenskaper,Medicinska fakulteten,Region Östergötland, Onkologiska kliniken US
Skeie-Jensen, Tone (author)
Oslo University Hospital, Norway
Hjerpe, Elisabet (author)
Karolinska Institutet,University of Southern Denmark, Denmark
Dorum, Anne (author)
Oslo University Hospital, Norway
Gebski, Val (author)
University of Sydney, Australia
Kristensen, Gunnar (author)
Oslo University Hospital, Norway; University of Oslo, Norway
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 (creator_code:org_t)
2017-01-24
2017
English.
In: British Journal of Cancer. - : NATURE PUBLISHING GROUP. - 0007-0920 .- 1532-1827. ; 116:4, s. 455-463
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: Chemotherapy in platinum-resistant ovarian cancer (PROC) aims for palliation and prolonging of progression-free survival (PFS). This study compares Health-related Quality of Life (HRQoL) and efficacy between single-agent chemotherapy and tamoxifen in PROC. Methods: Patients with PROC were randomised (2 : 1) to chemotherapy (weekly paclitaxel 80 mg m(-2) or four weekly pegylated liposomal doxorubicin 40 mg m(-2)) or tamoxifen 40mg daily. The primary end point was HRQoL. Secondary end points were PFS by RECIST and overall survival (OS). Results: Between March 2002 and December 2007, 156 and 82 patients were randomised to chemotherapy and tamoxifen, respectively. In the chemotherapy arm, a significantly larger proportion of patients experienced a worsening in their social functioning. There was no difference in the proportion of patients experiencing improvement of gastrointestinal symptoms. Median PFS on tamoxifen was 8.3 weeks (95% CI, 8.0-10.4) compared with 12.7 weeks (95% CI, 9.0-16.3) on chemotherapy (HR, 1.54; 95% CI, 1.16-2.05; log-rank P = 0.003). There was no difference in OS between the treatment arms. Conclusions: Patients on chemotherapy had longer PFS but experienced more toxicity and poorer HRQoL compared with tamoxifen. Control over gastrointestinal symptoms was not better on chemotherapy. These data are important for patient counselling and highlight the need to incorporate HRQoL end points in studies of PROC.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kirurgi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Surgery (hsv//eng)

Keyword

platinum-resistent ovarian cancer; chemotherapy; tamoxifen; quality of life; survival; phase III

Publication and Content Type

ref (subject category)
art (subject category)

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