Overview

Pyrotinib Plus Capecitabine Versus Lapatinib Plus Capecitabine in Patients With HER2+ Metastatic Breast Cancer. (PHOEBE)

Status:
Active, not recruiting

Trial end date:
2021-03-01

Target enrollment:
0

Participant gender:
All

Summary

Pyrotinib is an oral tyrosine kinase inhibitor targeting both HER-1 and HER-2 receptors. This study is a randomized,open-label,multi-center,active-controlled, parallel design study of the combination of pyrotinib and capecitabine versus Lapatinib plus capecitabine in HER2+ MBC patients, who have prior received taxane and trastuzumab.Patients will be randomized in a 1:1 ratio to one of the following treatment arms.Arm A: pyrotinib (400 mg once daily) + capecitabine (1000 mg/m^2 twice daily),Arm B: Lapatinib (1250 mg once daily) + capecitabine (1000 mg/m^2 twice daily).Patients will receive either arm of therapy until disease progression, unacceptable toxicity, or withdrawalof consent.

Phase:

Phase 3

Accepts Healthy Volunteers?

Details

Lead Sponsor:

Jiangsu HengRui Medicine Co., Ltd.

Treatments:

Capecitabine
Lapatinib

Criteria

Inclusion Criteria:

1. Aged ≥18 and ≤70 years.

2. ECOG performance status of 0 to 1.

3. Life expectancy of more than 12 weeks.

4. According to RECIST 1.1, at least one measurable lesion exists

5. Histologically or cytologic confirmed HER2 positive metastatic breast cancer.

6. Prior treatment with trastuzumab (≥2 cycles in metastatic setting, or

≥3 months in adjuvant/neoadjuvant setting) and Taxane(≥2 cycles in any setting or
untill unendurable AE or progression during treatment).

7. Previously reveived ≤2 chemotherapy regimens in metastasis setting;

8. Required laboratory values including following parameters:

ANC: ≥ 1.5 x 10^9/L; Platelet count: ≥ 90 x 10^9/L; Hemoglobin: ≥ 90 g/L; Total
bilirubin: ≤ 1.5 x upper limit of normal (ULN); ALT and AST: ≤ 2 x ULN(patients with
liver metastases: ≤5 x ULN); BUN and Creatinine:

≤ 1x ULN;CCR≥50 mL/min;LVEF: ≥ 50%;QTcF: < 450 ms (male)，< 470 ms（female）;

9. Signed informed consent.

Exclusion Criteria:

1. Received capecitabine in metastatic setting;

2. Received HER2 targeted tyrosine kinase inhibitor (including Lapatinib, Neratinib and
Pyrotinib);

3. Cumulated dosage of Doxorubincin >400 mg/m^2 or Epirubicin >800 mg/m^2 or equal dosage
of other anthracycline drugs in adjuvant/neoadjuvant/metastatic setting );

4. Received surgery，chemotherapy,radiotherapy or target therapy within 28 days prior to
randomization. Received hormone therapy within 7 days prior to randomization;

5. Participated in other clinical trial within 28 days prior to randomization.

6. Known dihydro pyrimidine dehydrogenase（DPD）defect;

7. CT or MRI confirmed brain metastases;

8. Bone or skin lesion as unique target lesion;

9. Second malignancies within 5 years, except for cured skin basal cell
carcinoma,carcinoma in-situ of uterine cervix and squamous-cell carcinoma;

10. Factors influencing the usage of oral administration (e.g. unable to swallow, chronic
diarrhea and intestinal obstruction, etc.);

11. Uncontrolled third space effusion (such as pleural fluid and ascites) by drainage or
other clinical intervention;

12. Receiving any other anti-tumour therapy after informed consent;

13. Unprogressed after or during the last anti-tumour therapy,according to RECIST1.1;

14. History of any kind of Heart disease,including 1)Angina pectoris; (2) Arrhythmia
required medication or with clinical significance; (3) Myocardial infarction; (4)
Heart failure; (5) Any other heart disease judged by researcher as not suitable for
participating in this study, etc;

15. History of Immunodeficiency, acquired or congenital immunodeficiency (HIV positive)
,history of organ transplantation;

16. History of neurological or psychiatric disorders, including epilepsy or dementia;

17. Concomitant disease judged by investigators that may bring serious harm to the safety
of patients or the completion of this study;

18. All female patients in breastfeeding period or in child-bearing period or with
positive pregnancy test result or refusing to take a reliable method of birth control
during the study;

19. Any other situations judged by investigator as not suitable for participating in this
study.