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The efficacy of irinotecan, paclitaxel, and oxaliplatin (IPO) in relapsed germ cell tumours with high-dose chemotherapy as consolidation: a non-cisplatin-based induction approach.
Badreldin, Waleed; Krell, Jonathan; Chowdhury, Simon; Harland, Stephen J; Mazhar, Danish; Harding, Victoria; Frampton, Adam E; Wilson, Peter; Berney, Daniel; Stebbing, Justin; Shamash, Jonathan.
Afiliação
  • Badreldin W; St Bartholomew's Hospital, London, UK.
  • Krell J; Charing Cross Hospital, London, UK.
  • Chowdhury S; Guy's and St. Thomas' NHS Foundation Trust, London, UK.
  • Harland SJ; University College London Cancer Institute, London, UK.
  • Mazhar D; Addenbrooke's Hospital, Cambridge, UK.
  • Harding V; Charing Cross Hospital, London, UK.
  • Frampton AE; Charing Cross Hospital, London, UK.
  • Wilson P; Charing Cross Hospital, London, UK.
  • Berney D; St Bartholomew's Hospital, London, UK.
  • Stebbing J; Charing Cross Hospital, London, UK.
  • Shamash J; St Bartholomew's Hospital, London, UK.
BJU Int ; 117(3): 418-23, 2016 Mar.
Article em En | MEDLINE | ID: mdl-25430674
ABSTRACT

OBJECTIVES:

To determine the outcome of an expanded cohort of patients with relapsed germ cell tumours (GCTs) treated with a salvage chemotherapy regimen consisting of irinotecan, paclitaxel and oxaliplatin (IPO) and assess the role of IPO as an alternative to standard cisplatin-based chemotherapy regimens in this setting. PATIENTS AND

METHODS:

The results of 72 consecutive patients were reviewed retrospectively. IPO was used either as a second-line treatment (29 patients), of which 20 patients subsequently received high-dose chemotherapy (HDCT), or third-line (43), of which 32 patients proceeded to HDCT.

RESULTS:

The 2-year progression-free survival (PFS) and 3-year overall survival (OS) rates for the whole cohort were 30.2% (95% confidence interval [CI] 17.3-40.5%) and 33.4% (95% CI 20.1-43.8%), respectively. Complete remission was achieved in 3%, marker-negative partial response (PR) in 41%, marker-positive PR in 18%, stable disease in 17% and progressive disease in 20%. In the second-line setting, the 2-year PFS rate was 43.5% (95% CI 21.7-60.8%) and 3-year OS 49.1% (95% CI 24.2-65.1%). In the third-line setting, the 2-year PFS rate was 21.0% (95% CI 9.5-35.4%) and the 3-year OS rate was 23.9% (95% CI 11.7-38.2). According to the current international prognostic factor study group criteria for first relapse for the high- and very high-risk group the 2-year PFS rates were 50% and 30%, respectively. There were two treatment-related deaths from IPO, and four from HDCT. Grade 3 or 4 toxicities included neutropenia (35%), thrombocytopaenia (18%), infection (15%), diarrhoea (11%) and lethargy (8%).

CONCLUSIONS:

IPO offers an effective, well-tolerated, non-nephrotoxic alternative to cisplatin-based salvage regimens for patients with relapsed GCTs. It appears particularly useful in high-risk patients and for those in whom cisplatin is ineffective or contra-indicated.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Embrionárias de Células Germinativas Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Humans / Male / Middle aged Idioma: En Revista: BJU Int Assunto da revista: UROLOGIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Neoplasias Embrionárias de Células Germinativas Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Humans / Male / Middle aged Idioma: En Revista: BJU Int Assunto da revista: UROLOGIA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Reino Unido