Literature DB >> 19853437

Prognostic and predictive factors for outcome to first-line ifosfamide-containing chemotherapy for adult patients with advanced soft tissue sarcomas: an exploratory, retrospective analysis on large series from the European Organization for Research and Treatment of Cancer-Soft Tissue and Bone Sarcoma Group (EORTC-STBSG).

Stefan Sleijfer1, Monia Ouali, Martine van Glabbeke, Anders Krarup-Hansen, Sjoerd Rodenhuis, Axel Le Cesne, Pancras C W Hogendoorn, Jaap Verweij, Jean-Yves Blay.   

Abstract

BACKGROUND: Adult patients with advanced soft tissue sarcomas (STS) are generally treated similarly, regardless of great differences between STS subtypes, disease presentation and patients' characteristics. As ifosfamide is frequently applied in first line systemic therapy, we aimed to establish prognostic and predictive factors for outcome to ifosfamide-based therapy.
METHODS: A retrospective, exploratory analysis was performed on data from 1337 advanced STS patients who received first-line ifosfamide-containing chemotherapy. For predictive factor analysis, 660 patients treated with doxorubicin monotherapy served as comparators.
RESULTS: Independent favourable prognostic factors for overall survival (OS) were good performance status, female gender, low histological grade, extremity primary tumour site and locally advanced disease; for progression-free survival (PFS), the combination of doxorubicin and ifosfamide, locally advanced disease, and tumour entity with a lower risk to progress for synovial sarcoma patients compared to leiomyosarcoma. For response, independent favourable prognostic factors were doxorubicin combined with ifosfamide, higher histological grade, and histology with synovial sarcoma patients having the highest chance to respond. Predictive factor analysis showed that compared to doxorubicin monotherapy, patients who benefited less from ifosfamide-based therapies were leiomyosarcoma patients in terms of OS, and patients with liposarcoma for response. No predictive factors were found for PFS.
CONCLUSION: In this study, we established an independent set of prognostic and predictive factors for outcome to ifosfamide-based chemotherapy in advanced STS patients. This study provides important information for the interpretation and design of clinical trials for specific STS entities and may contribute to further treatment individualisation of advanced STS patients.

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Year:  2010        PMID: 19853437     DOI: 10.1016/j.ejca.2009.09.022

Source DB:  PubMed          Journal:  Eur J Cancer        ISSN: 0959-8049            Impact factor:   9.162


  68 in total

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4.  Outcomes of Elderly Patients with Advanced Soft Tissue Sarcoma Treated with First-Line Chemotherapy: A Pooled Analysis of 12 EORTC Soft Tissue and Bone Sarcoma Group Trials.

Authors:  Eugenie Younger; Saskia Litière; Axel Le Cesne; Olivier Mir; Hans Gelderblom; Antoine Italiano; Sandrine Marreaud; Robin Lewis Jones; Alessandro Gronchi; Winette T A van der Graaf
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Authors:  Rashi Bharat Patel; Ting Li; Zhichao Liao; Jivani Aakash Jaldeepbhai; H A Pavanika N V Perera; Sujani Kaushalya Muthukuda; Dholiya Hardeep Dhirubhai; Vaibhav Singh; Xiaoling Du; Jilong Yang
Journal:  Stem Cell Investig       Date:  2017-03-15

6.  Long-term responders and survivors on pazopanib for advanced soft tissue sarcomas: subanalysis of two European Organisation for Research and Treatment of Cancer (EORTC) clinical trials 62043 and 62072.

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Review 7.  Current status of engineered T-cell therapy for synovial sarcoma.

Authors:  Matthew Dallos; William D Tap; Sandra P D'Angelo
Journal:  Immunotherapy       Date:  2016-09       Impact factor: 4.196

8.  Leiomyosarcoma: Principles of management.

Authors:  Juan Martin-Liberal
Journal:  Intractable Rare Dis Res       Date:  2013-11

9.  Low level of baseline circulating VEGF-A is associated with better outcome in patients with vascular sarcomas receiving sorafenib: an ancillary study from a phase II trial.

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Journal:  Target Oncol       Date:  2013-11-12       Impact factor: 4.493

Review 10.  Children's Oncology Group's 2013 blueprint for research: Soft tissue sarcomas.

Authors:  Douglas S Hawkins; Sheri L Spunt; Stephen X Skapek
Journal:  Pediatr Blood Cancer       Date:  2012-12-19       Impact factor: 3.167

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