Cancer Res Treat.  2015 Jul;47(3):406-415. 10.4143/crt.2014.073.

A Randomized Phase II Trial of Capecitabine Plus Vinorelbine Followed by Docetaxel Versus Adriamycin Plus Cyclophosphamide Followed by Docetaxel as Neoadjuvant Chemotherapy for Breast Cancer

Affiliations
  • 1Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. drjiny@amc.seoul.kr
  • 2Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • 3Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • 4Department of Radiation Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • 5Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

Abstract

PURPOSE
Given the promising activity of capecitabine and vinorelbine in metastatic breast cancer, this randomized phase II trial evaluated the efficacy and safety of this combination as neoadjuvant chemotherapy in breast cancer.
MATERIALS AND METHODS
Patients with operable breast cancer (n=75) were randomly assigned to receive either four cycles of adriamycin 60 mg/m2 plus cyclophosphamide 600 mg/m2 every 3 weeks followed by four cycles of docetaxel 75 mg/m2 every 3 weeks (AC-D) or four cycles of capecitabine 2,000 mg/m2 (day 1-14) plus vinorelbine 25 mg/m2 (days 1 and 8) every 3 weeks followed by four cycles of docetaxel 75 mg/m2 (CV-D). The primary endpoint was pathologic complete response (pCR) in the primary breast (ypT0/is).
RESULTS
Most patients (84%) had locally advanced (n=41) or inflammatory breast cancer (n=22). pCR rates in the primary breast were 15% (95% confidence interval [CI], 7% to 30%) and 11% (95% CI, 4% to 26%) in the AC-D and CV-D groups, respectively. The overall response rates and 5-year progression-free survival rates in the AC-D and CV-D groups were 62% and 64%, and 51.3% (95% CI, 34.6% to 68.0%) and 30.2% (95% CI, 13.3% to 47.1%), respectively. Although both regimens were well tolerated, CV-D showed less frequent grade 3-4 neutropenia and vomiting than AC-D, whereas manageable diarrhea and hand-foot syndrome were more common in the CV-D group.
CONCLUSION
CV-D is a feasible and active non-anthracycline-based neoadjuvant chemotherapy regimen for breast cancer.

Keyword

Breast neoplasm; Neoadjuvant therapy; Anthracyclines; Capecitabine; Vinorelbine

MeSH Terms

Anthracyclines
Breast
Breast Neoplasms*
Cyclophosphamide*
Diarrhea
Disease-Free Survival
Doxorubicin*
Drug Therapy*
Hand-Foot Syndrome
Humans
Inflammatory Breast Neoplasms
Neoadjuvant Therapy
Neutropenia
Polymerase Chain Reaction
Vomiting
Anthracyclines
Cyclophosphamide
Doxorubicin

Figure

  • Fig. 1. Consolidated Standards of Reporting Trials (CONSORT) diagram. AC-D, anthracycline and cyclophosphamide followed by docetaxel; CV-D, capecitabine and vinorelbine followed by docetaxel.

  • Fig. 2. Progression-free survival (A) and overall survival (B). AC-D, anthracycline and cyclophosphamide followed by docetaxel; CV-D, capecitabine and vinorelbine followed by docetaxel.

  • Fig. 3. Relative dose intensity of docetaxel. AC-D, anthracycline and cyclophosphamide followed by docetaxel; CV-D, capecitabine and vinorelbine followed by docetaxel.


Reference

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