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Initial dose intensity has limited impact on the outcome of ABVD chemotherapy for advanced Hodgkin lymphoma (HL): data from UKLG LY09 (ISRCTN97144519).
Owadally, W S; Sydes, M R; Radford, J A; Hancock, B W; Cullen, M H; Stenning, S P; Johnson, P W M.
Afiliação
  • Owadally WS; Cancer Sciences Division, Cancer Research UK Clinical Centre, Southampton.
  • Sydes MR; Cancer Division, Medical Research Council Clinical Trials Unit, London.
  • Radford JA; Department of Medical Oncology, Christie Hospital, Manchester.
  • Hancock BW; Department of Medical Oncology, Weston Park Hospital, Sheffield.
  • Cullen MH; Cancer Centre, Birmingham University Hospitals, Birmingham, UK.
  • Stenning SP; Cancer Division, Medical Research Council Clinical Trials Unit, London.
  • Johnson PWM; Cancer Sciences Division, Cancer Research UK Clinical Centre, Southampton. Electronic address: johnsonp@soton.ac.uk.
Ann Oncol ; 21(3): 568-573, 2010 Mar.
Article em En | MEDLINE | ID: mdl-19684105
ABSTRACT

BACKGROUND:

This analysis was undertaken to assess the relationship between the dose intensity (DI) of initial chemotherapy and outcome in a large cohort of patients with advanced Hodgkin lymphoma treated in a randomised controlled trial, in which detailed dose data were collected prospectively. PATIENTS AND

METHODS:

Three-hundred and eighty patients randomly assigned to receive standard doxorubicin, bleomycin, vinblastine and dacarbazine who underwent at least two cycles of treatment were studied. With a median follow-up of 6.9 years, progression-free survival (PFS) from the end of cycle 2 was analysed according to DI during those cycles.

RESULTS:

During the first two cycles, 25% of patients received >97% of planned DI, 37% received between 86% and 97% and 38% received <86%. DI during the first two cycles was correlated with DI during the remainder of the course, but there was no evidence that early DI influenced PFS (hazard ratio 0.87, 95% confidence interval 0.67-1.11; P = 0.265). Multivariate analysis also failed to confirm the influence of early DI on PFS or overall survival.

CONCLUSIONS:

At the range of DI delivered in a multicentre trial using conventional therapy, there is no clear evidence that early DI influences outcome. This should be tested in a prospective study.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Hodgkin / Protocolos de Quimioterapia Combinada Antineoplásica Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Adult / Humans / Middle aged Idioma: En Ano de publicação: 2010 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Hodgkin / Protocolos de Quimioterapia Combinada Antineoplásica Tipo de estudo: Clinical_trials / Observational_studies / Risk_factors_studies Limite: Adult / Humans / Middle aged Idioma: En Ano de publicação: 2010 Tipo de documento: Article