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OpenTrials
Completed

NCT Number: NCT02860585

Evaluation of Survival in Patients With Metastatic Breast Cancer Receiving High-dose Chemotherapy With Autologous Haematopoietic Stem Cell Transplantation

The objective of this study was to evaluate the outcome of patients affected with different subtypes of metastatic breast cancer following treatment with high-dose chemotherapy and autologous haematopoietic progenitor cell transplantation.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Institut Paoli-Calmettes

Marseille, 13009, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age>18 years
  • Metastatic breast Cancer
  • Treatment with high-dose chemotherapy and autologous haematopoietic progenitor cell transplantation between 2003 and 2012

Exclusion criteria

  • Lack of follow-up data

Treatment and study plan

Primary outcomes

  1. Overall Survival according to Immunohistochemical subtypes .

    Time frame: 8 years

Secondary outcomes

  1. Progression free Survival according to Immunohistochemical subtypes .

    Time frame: 8 years

Sponsors and collaborators

Lead sponsor

Institut Paoli-Calmettes

Other

Registry information

Acronym: BREAST-HDCT

Important dates

Study start
2013
Primary completion
2016
Study completion
2016
First posted
Aug 9, 2016
Registry last updated
Sep 26, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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