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Health-related quality of life in recurrent platinum-sensitive ovarian cancer--results from the CALYPSO trial.
Brundage, M; Gropp, M; Mefti, F; Mann, K; Lund, B; Gebski, V; Wolfram, G; Reed, N; Pignata, S; Ferrero, A; Brown, C; Eisenhauer, E; Pujade-Lauraine, E.
Afiliação
  • Brundage M; NCIC Clinical Trials Group; Department of Medical Oncology, Queen's University, Kingston, Canada. Electronic address: michael.brundage@krcc.on.ca.
  • Gropp M; Department of Medical Oncology, AGO, Düsseldorf, Germany.
  • Mefti F; Department of Medical Oncology, GINECO, Saint-Cloud, France.
  • Mann K; Department of Medical Oncology, National Health and Medical Research Council Clinical Trials Centre, Sydney, Australia.
  • Lund B; Department of Oncology, Aalborg Hospital, Aalborg, Denmark.
  • Gebski V; National Health and Medical Research Council Clinical Trials Centre, University of Sydney, Sydney, Australia.
  • Wolfram G; Department of Gynecology, Arbeitsgemeinschaft Gynaekologische Onkologie-Austria, Ried, Austria.
  • Reed N; Beatson Oncology Centre, Gartnavel General Hospital, Glasgow, UK.
  • Pignata S; Multicenter Italian Trials in Ovarian Cancer (MITO), Napoli.
  • Ferrero A; Academic Division of Gynecologic Oncology, Mauriziano Hospital, Torino, Italy.
  • Brown C; NHMRC Clinical Trials Centre, Sydney, Australia.
  • Eisenhauer E; NCIC Clinical Trials Group; Department of Medical Oncology, Queen's University, Kingston, Canada.
  • Pujade-Lauraine E; Department of Oncology, Hôpital Hôtel-Dieu, Paris, France.
Ann Oncol ; 23(8): 2020-2027, 2012 Aug.
Article em En | MEDLINE | ID: mdl-22291207
ABSTRACT

BACKGROUND:

In the CALYPSO trial, carboplatin-pegylated liposomal doxorubicin (CD) demonstrated superior therapeutic index versus carboplatin-paclitaxel (CP) in patients with recurrent ovarian cancer. This paper reports the health-related quality of life (HRQoL) findings. MATERIALS AND

METHODS:

HRQoL was measured with the EORTC QoL-QC30 questionnaire and OV28 ovarian cancer module. Mean change scores from baseline in HRQoL subscales (five functional scales and global health status) in each arm and the proportion of patients improved or worsened were calculated every 3 months until 12 months.

RESULTS:

Compliance was 90% at baseline and 76%, 64%, 57% at 3, 6, and 9 months, respectively. Baseline HRQoL showed already impaired global scores (mean 62/100) and considerable symptom burden (90% of patients reporting nonzero scores). Global QoL and abdominal symptom scores improved over time in both arms; at 6 months, 36% of patients met criteria for improved symptoms. Treatment with CD resulted in less peripheral neuropathy (9.8 versus 24.2), fewer other chemotherapy side-effects (9.5 versus 16.2), and less impact on body image (3.8 versus 10.4) versus CP (all P<0.02) at 6 months.

CONCLUSIONS:

These patient-reported outcomes confirm the overall lower toxicity of CD versus CP. The improved disease-related outcomes achieved with CD were not at the expense of QoL.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Protocolos de Quimioterapia Combinada Antineoplásica / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials / Diagnostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2012 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Protocolos de Quimioterapia Combinada Antineoplásica / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials / Diagnostic_studies Limite: Female / Humans Idioma: En Ano de publicação: 2012 Tipo de documento: Article