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Observed benefit and safety of aflibercept in elderly patients with metastatic colorectal cancer: An age-based analysis from the randomized placebo-controlled phase III VELOUR trial

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11130%2F18%3A10375404" target="_blank" >RIV/00216208:11130/18:10375404 - isvavai.cz</a>

  • Alternative codes found

    RIV/00064203:_____/18:10375404 RIV/00209805:_____/18:00078107

  • Result on the web

    <a href="https://doi.org/10.1016/j.jgo.2017.07.010" target="_blank" >https://doi.org/10.1016/j.jgo.2017.07.010</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jgo.2017.07.010" target="_blank" >10.1016/j.jgo.2017.07.010</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Observed benefit and safety of aflibercept in elderly patients with metastatic colorectal cancer: An age-based analysis from the randomized placebo-controlled phase III VELOUR trial

  • Original language description

    Objectives: Aflibercept (ziv-aflibercept) significantly improves progression-free (PFS) and overall survival (OS) when added to 5-fluorouracil, leucovorin and irinotecan (FOLFIRI), compared with FOLFIRI alone, in patients with metastatic colorectal cancer previously treated with oxaliplatin-based therapy. This subset analysis of the VELOUR study investigates aflibercept plus FOLFIRI versus placebo plus FOLFIRI according to age. Methods: Efficacy and safety were analyzed by treatment arm and age (&gt;= or &lt;65 years). Results: Overall, 443 patients were 65 years old (205 in aflibercept arm; 238 in placebo arm) and 783 were &lt;65 years old (407 in aflibercept arm; 376 in placebo arm). Median OS was 12.6 versus 11.3 months (hazard ratio [HR]: 0.85; 95.34% CI 0.68-1.07) in patients &gt;= 65 years old and 14.5 versus 12.5 months (HR: 0.80; 95.34% CI 0.67-0.95) in those patients &lt;65 years old, for patients receiving FOLFIRI plus aflibercept or placebo, respectively. There was no interaction between treatment and age. Treatment-emergent adverse events (AEs) were comparable for patients &lt;65 years and &gt;= 65 years old. The incidence of grade 3/4 AEs was higher for patients &gt;= 65 years old than for those &lt;65 years old in both the aflibercept (89.3% versus 80.5%) and placebo (67.4% versus 59.4%) arms. Interaction tests for grade 3/4 antiangiogenic agent-related AEs suggested no heterogeneity between the older and younger patient populations (p &gt; 0.1). Conclusion: A limited but consistent benefit on both OS and PFS was associated with the addition of aflibercept to FOLFIRI compared with placebo in patients &lt;65 and &gt;= 65 years old, with a marked but manageable increase in the toxicity profile in older patients.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30204 - Oncology

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Geriatric Oncology

  • ISSN

    1879-4068

  • e-ISSN

  • Volume of the periodical

    9

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    8

  • Pages from-to

    32-39

  • UT code for WoS article

    000422701400006

  • EID of the result in the Scopus database

    2-s2.0-85028304694