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Completed

NCT Number: NCT03888677

Dose-adjusted Adjuvant FEC Compared to Standard FEC for Breast Cancer

This is an open randomized phase III study. The primary objective of this study is to compare FEC adjuvant chemotherapy in operable breast cancer given either as fixed doses calculated according to the patients surface area or with doses adjusted according to leukopenia after course one in order to achieve hematological equitoxicity. The main aim of the study is to test whether chemotherapy dosage aimed at hematological equitoxicity will improve the effect of adjuvant chemotherapy.

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Key information

Age range

18 year–60 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

About this study

Group A, FECStandard(standard FEC) is given 7 courses of 5-fluorouracil-epirubicin (Farmorubicin)-cyclophosphamide with doses based on the patient's surface area. Leukocyte nadir values at day 10, 12 or 13 and 15 are measured. Dose-reductions of one step according to table 8.2.1 are performed in case of leukopenic fever or grade 4 leukopenia.

Group B FECTailored(Tailored FEC) receives course one at identical doses to group A. Leukocyte nadir values at day 10,12 or 13 and 15 are measured. Doses of subsequent courses are adjusted to achieve grade 3 leukopenia (leukocyte nadir 1.0 to 2.0) in patients experiencing only grade 0 to 2 leukopenia after course one.

Dose-reductions of one step according to table 8.2.1 are performed in case of leukopenic fever or grade 4 leukopenia .

Patients achieving only grade 0-2 leukopenia at the first course will be randomized into continued treatment at standard doses (Group A) or to doses tailored to achieve grade 3 leukopenia (Group B). The primary comparisons will be made between these two groups of patients.

Patients with grade 3-4 leukopenia after the first course not be randomized but followed according to the protocol and received treatment as group A, FECStandard.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Node positive or 2) High-risk node negative#
  • no major cardiovascular morbidity
  • female age 18-60
  • ECOG/WHO performance status <1
  • histologically proven invasive breast cancer
  • written or oral witnessed informed consent according to the local Ethics Committee requirements
  • start of adjuvant chemotherapy within 8 weeks after surgery

Exclusion criteria

  • distant metastases (M1)
  • locally advanced cancer
  • nonradically operated (positive resection margins)
  • pregnancy or lactation
  • leukocyte count < 3.5 x109 /l
  • platelets < 100 x109 /l
  • other serious medical condition
  • previous or concurrent malignancies at other sites, except basal cell carcinoma and carcinoma cervicis uteri in situ

Treatment and study plan

5-FU, epirubicin and cyclophosphamide

Drug

Tailored dose escalation of epirubicin and cyclophosphamide.

Primary outcomes

  1. Distant disease-free survival.

    Time frame: 5-10 years

    Distant disease-free survival comparing standard and tailored arm.

Secondary outcomes

  1. Regio-locally relapsed disease

    Time frame: 5-10 years

    Regiolocal disease-free survival

  2. Overall survival

    Time frame: 5-10 years

    Overall survival

  3. Toxicity of treatment.

    Time frame: 5-10 years

    Adverse events

  4. Leukopenia and correlation to prognosis in distant disease-free survival.

    Time frame: 5-10 years.

    Distant disease-free survival in patients groups based on nadir leukopenia after third cycle.

  5. Effect of dose escalation of leukopenia and correlation to prognosis in distant disease-free survival.

    Time frame: 5-10 years.

    Comparing distant disease-free survival difference between patients randomized to tailored and dose-escalated FEC with the Group of patients with standard FEC but with similar grade of leukopenia.

Sponsors and collaborators

Lead sponsor

Henrik Lindman

Other

Collaborators

  • Danish Breast Cancer Cooperative Group
  • Pharmacia Pharmaceutical Company
  • Scandinavian Breast Group
  • Swedish Breast Cancer Group
  • Swedish Cancer Foundation
  • Swedish Cancer Society

Registry information

Official study title

SBG 2000-1. Individually Dose-adjusted FEC Compared to Standard FEC as Adjuvant Chemotherapy for Node Positive or High-risk Node Negative Breast Cancer. A Randomized Study by the Scandinavian Breast Group

Important dates

Study start
2001
Primary completion
2003
Study completion
2014
First posted
Mar 25, 2019
Registry last updated
Mar 28, 2019

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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