Know Cancer

forgot password

A Randomized, Open-Label Trial Comparing Treatment With Either Pegylated Liposomal Doxorubicin or Capecitabine as First Line Chemotherapy for Metastatic Breast Cancer (PELICAN Trial)

Phase 3
18 Years
Not Enrolling
Breast Cancer

Thank you

Trial Information

A Randomized, Open-Label Trial Comparing Treatment With Either Pegylated Liposomal Doxorubicin or Capecitabine as First Line Chemotherapy for Metastatic Breast Cancer (PELICAN Trial)

Inclusion Criteria:

- Patients must be female.

- Patients must have metastatic disease of a cytological or histological confirmed
breast cancer.

- Patients must be 18 years or older.

- Patients should have evaluable disease (at least uni-dimensionally measurable lesion
according to the RECIST criteria in at least one site that has not been irradiated),
however, patients who only have non-measurable/evaluable disease are not excluded.
Also patients with only bone metastasis are not excluded.

- Patients must have an Eastern Cooperative Oncology Group (ECOG) 0-2.

- Patients must have a sufficient life expectancy to be treated with chemotherapy.

- Patients must be willing and able to complete study questionnaires.

- Patients must have adequate renal function as evidenced by serum creatinine <=1.5
mg/dL, or a creatinine clearance of >=45 mL/min (if serum creatinine is > 1.5 mg/dL
but <= 1.8 mg/dL).

- Patients must have adequate bone marrow function as evidenced by leukocyte count
greater than 3.5 g/L, hemoglobin >=9.0 g/dL, and platelet count >=100x10^9/L.

- Patients must have adequate liver function as evidenced by bilirubin of <=1.5 times
the upper limits of normal (ULN) and alkaline phosphatase <=3 times, ULN unless
related to liver metastasis.

- Patients must have Sodium and Potassium values within normal limits.

- Patients whose clinical condition (co-morbidity) allows a treatment with monotherapy
or who expressed their wish to be treated with monotherapy.

- Patients must have signed an informed consent document indicating that they
understand the purpose of and procedures required for the study and are willing to
participate in the study.

Exclusion Criteria:

- History of receiving prior chemotherapy in the metastatic setting (Note: patients may
have had hormonal therapy or chemotherapy in the adjuvant setting; patients may have
received hormonal therapy in metastatic setting, patients may have received local

- Patients with positive estrogen- / progesterone-receptor status, where an endocrine
therapy is indicated. However, patients progressing under hormonal therapy are not

- Patients with known hypersensitivity to doxorubicinhydrochlorid or to any of the
excipients OR known hypersensitivity to capecitabine or fluorouracil or to any of the

- Patients with known DPD (dihydro pyrimidine dehydrogenase) deficiency.

- Patients who are receiving a concomitant treatment with sorivudine or its chemically
related analogues, such as brivudine.

- Patients who are taking concomitant medications (except bisphosphonates) for
metastatic disease, including hormonal therapy, radiation therapy, trastuzumab, or
biologicals are also not permitted.

- Patients with Human epidermal growth factor receptor 2 (Her-2/neu) overexpressing
tumors with the most recent evaluation as the relevant result

- immunologically Her2neu 3+ positive

- Her2neu-2+ positive and ´Fluorescent in-situ hybridization (FISH)´ positive

- History of treatment with capecitabine

- History of treatment with anthracyclines in the adjuvant setting exceeding cumulative
doses of anthracyclines by more than 360 mg/m^2 doxorubicin (or equivalents, i.e.
600mg/m^2 epirubicine).

- Patients with anthracycline resistant disease are not permitted. Anthracycline
resistance is defined as development of locally recurrent or metastatic disease while
on adjuvant anthracycline therapy, or relapse less than 12 months after completion of
anthracycline therapy.

- Strong remission pressure that requires polychemotherapy with the exception of
patients who are not suitable for a treatment with polychemotherapy or not accepting

- Evidence of primary or metastatic malignancy involving the central nervous system
unless previously treated and asymptomatic for 3 months or greater.

- Patients with reduced liver functions (evidenced by bilirubin of above 1.5 times the
upper limits of normal (ULN); alkaline phosphatase above 3 times ULN (except related
to liver metastasis, in which case <=5 x ULN).

- Dyspnea on exertion.

- History of cardiac disease, with New York Heart Association Class II or greater, or
clinical evidence of congestive heart failure or myocardial infarct within less than
six months or an left ventricular ejection fraction (LVEF) below 50%.

- Woman with childbearing potential with insufficient contraception [e.g. intra-uterine
device (IUD) are regarded as sufficient] during the study period and the six months
following the last study drug application. All methods based on hormonal
contraception are not permitted.

- Existing pregnancy or lactation (note on pregnancy test). A negative pregnancy test
for women of childbearing potential has to be in place prior randomization (Note: A
pregnancy test has to be done for patients who are not postmenopausal. Postmenopausal
is defined as those not having a menstrual period for 12 months in a row).

- Existing doubts on ability and willingness of the subject for cooperation.

- Participation of the subject at a clinical study within the last 30 days.

- Participation of the subject in the same clinical study at an earlier date.

- Concomitant participation in another study than the one described here.

- Abuse of drugs, alcohol, or pharmaceuticals.

- Any condition, whether medical or non-medical, that may interfere, in the opinion of
the investigator, with aim of this study.

Type of Study:


Study Design:

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Time to Disease Progression (TTP) Using Response Evaluation Criteria in Solid Tumors (RECIST)

Outcome Description:

TTP was defined as the time from onset of treatment with study drug until first evidence/diagnosis of progressive disease or - in the absence of any diagnosis of progressive disease - until the participant´s death. Diagnosis of progressive disease was done according to RECIST (Version 1.0) and/or investigator assessment based on RECIST. RECIST criteria used changes in the largest diameter of target/non-target lesions. Target (measurable) lesions were up to a maximum of 5 per organ & >20 mm by clinical imaging (>=10 mm with spiral CT scan). Non-target lesions were all other lesions.

Outcome Time Frame:

From Day 1 (Cycle 1) until First Evidence/Diagnosis of Progressive Disease or Death

Safety Issue:



Germany: Federal Institute for Drugs and Medical Devices

Study ID:




Start Date:

January 2006

Completion Date:

October 2010

Related Keywords:

  • Breast Cancer
  • Breast Neoplasms