A Study to Evaluate Safety and Effectiveness of Bevacizumab in Combination With Paclitaxel and Cisplatin/Carboplatin or Toptecan in Participants With Advanced Cervical Cancer

  • Cancer
  • Cervical Cancer
Please note that the recruitment status of the trial at your site may differ from the overall study status because some study sites may recruit earlier than others.
Trial Status:

Completed

This trial runs in
Country
  • Argentina
Trial Identifier:

NCT03071848 ML39360

  • CENICLAR

    2493 San LuisS2002RosarioArgentina
  • Centro Medico San Roque

    579 BalcarceT4000San Miguel de TucumánArgentina
  • Centro Oncologico Riojano Integral (CORI)

    269 DorregoF5300La RiojaArgentina
  • Hosp Provincial D. Centenarios; Oncology Dept

    3101 UrquizaS2002Santa FeArgentina
  • Hospital General de Agudos J. A. Penna ; Breast Pathology

    C1437
  • Hospital General de Agudos Juan Antonio Fernandez

    3356 Av. CerviñoC1425Buenos AiresArgentina
  • Hospital Interzonal General De Agudos "Luisa C. de Gandulfo"

    351 BalcarceB1832Lomas de ZamoraArgentina
  • Hospital Julio C. Perrando

    1100 Av. 9 de JulioH3508ResistenciaArgentina
  • Hospital Pablo Soria

    1345 Gral. GüemesY4600San Salvador de JujuyArgentina
  • Hospital Privado de Comunidad; Oncology

    4545 CórdobaB7602Mar del PlataArgentina
  • Instituto Ángel H. Roffo - Universidad de Buenos Aires

    5481 Av. San MartínC1417dtbArgentina
  • Policlínico regional de San Luis

    225 Héroes de MalvinasD5700Villa MercedesArgentina
    Show trial locations

    The source of the below information is public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc.. It has been summarised and edited into simpler language. For more information about this clinical trial see the For Expert tab on the specific ForPatients page or follow these links to https://clinicaltrials.gov and/or https://euclinicaltrials.eu and/or https://www.isrctn.com.

    The below information is taken directly from public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc., and has not been edited.

    Results Disclaimer

    Trial Summary

    This study will evaluate the safety of bevacizumab (Avastin®) combined with standard chemotherapy in participant with advanced cervical cancer, with special focus on the incidence of gastrointestinal (GI) and genitourinary (GU) fistulas and GI perforations in the common practice setting.

    Hoffmann-La Roche Sponsor
    N/A Phase
    NCT03071848, ML39360 Trial Identifier
    No Intervention Treatments
    Cervical Cancer Condition
    Official Title

    Retrospective Multicenter Observational Study to Evaluate Safety and Effectiveness of Bevacizumab (Avastin®) in Combination With Paclitaxel and Cisplatin/Carboplatin or Toptecan in Patients With Advanced Cervical Cancer

    Eligibility Criteria

    Female Gender
    ≥ 18 Years Age
    No Healthy Volunteers
    Inclusion Criteria
    • Age 18 or older
    • Diagnosis of primary stage IVB, recurrent or persistent squamous cell carcinoma, adenosquamous carcinoma, or adenocarcinoma of the cervix which is not amenable to curative treatment with surgery and/or radiation therapy
    • Retrospective clinical decision made to initiate therapy with bevacizumab (Avastin®) combined with standard chemotherapy (cisplatin or carboplatin or topotecan and paclitaxel) between 01 January 2015 and 01 January 2016
    • All participants must have received at least one dose of bevacizumab combined with standard chemotherapy between 01 January 2015 and 01 January 2016 AND have at least 12 months of documented follow up, from treatment start, unless died or lost to follow up within the minimum study entry follow up period
    • Availability of documentation of for advanced cervical cancer (including prior treatment as applicable) and follow up in the participant's medical records
    Exclusion Criteria
    • Participation during the study period in an interventional clinical trial or any other interventional study that may impact advanced cervical cancer outcome
    • Participants who have received prior therapy with any anti‑VEGF drug, including bevacizumab

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