Evaluation of efficacy and toxicity of anthracycline plus cyclophosphamide every three weeks followed by weekly paclitaxel: The Izmır Oncology Group (IZOG) Study
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Original Article
P: 450-454
2019

Evaluation of efficacy and toxicity of anthracycline plus cyclophosphamide every three weeks followed by weekly paclitaxel: The Izmır Oncology Group (IZOG) Study

Acta Haematol Oncol Turc 2019;52(3):450-454
1. Department of Medical Oncology, Kahramanmaras Necip Fazıl City Hospital, Kahramanmaras, Turkey
2. Department of Internal Medicine, Izmir Katip Celebi University Ataturk Training and Research Hospital, Izmir, Turkey
3. Department of Medical Oncology, Izmir Katip Celebi University Ataturk Training and Research Hospital, Izmir, Turkey
4. Department of Internal Medicine, Izmir Demokrasi University, Izmir, Turkey
5. Institute of Oncology, Dokuz Eylul University, Izmir, Turkey
6.
No information available.
No information available
Received Date: 2019-06-23T18:07:08
Accepted Date: 2019-12-27T14:29:27
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Abstract

INTRODUCTION

Dose-dense chemotherapy (AC Q2×4→P Q2×4) is widely used in the adjuvant treatment of high-risk breast cancer patients. However, there is no direct comparison of dose-dense chemotherapy consisting of anthracycline plus cyclophosphamide every three weeks followed by weekly paclitaxel (AC Q3 × 4 → P W × 12) regimen. Moreover, when weekly paclitaxel is added to anthracycline plus cyclophosphamide, it is unknown whether or not dose-dense AC (AC Q2×4) is superior to conventional AC (AC Q3×4). The study aimed to evaluate the efficacy and toxicity of AC Q3 × 4 → P W × 12 regimen.

METHODS

Patients diagnosed with breast cancer from 2013 to 2016 were retrospectively evaluated. The study included women who had histologically-involved lymph nodes (tumor stage T1, T2, or T3 and nodal stage N1, N2, or N3) or high-risk, axillary node-negative disease (T2 or T3, N0) without distant metastases.

RESULTS

This study included 150 patients with breast cancer. After a median follow up period of 31 months, 13 patients had developed distant metastases and 6 patients had died. The estimated 5-year disease-free survival and overall survival rates were 88.4% and 92%, respectively. Severe neutropenia (grade 3, 4) occurred in 38.6%of the patients whereas no severe cardiotoxicity was observed.

DISCUSSION AND CONCLUSION

AC Q3 × 4 → P W × 12 regimen is well-tolerated and effective in patients with node-positive or high-risk node-negative early-stage breast cancer.