A phase II feasibility study of concurrent docetaxel chemotherapy and radiation to chest wall and peripheral lymphatics after four cycles of AC chemotherapy in patients with high risk operable breast cancer. A trial of the Pakistan Cancer Research Group

2005 ◽  
Vol 23 (16_suppl) ◽  
pp. 858-858
Author(s):  
A. Shaharyar ◽  
I. H. Shah ◽  
S. Abubaker ◽  
M. Hafeez ◽  
P. Shahina ◽  
...  
2006 ◽  
Vol 24 (18_suppl) ◽  
pp. 10684-10684
Author(s):  
I. H. Shah ◽  
A. Shaharyar ◽  
A. Shahid ◽  
M. Hafeez ◽  
S. Perveen ◽  
...  

10684 Background: Sequential use of docetaxel after four cycles of AC chemotherapy delays the postoperative radiation and can compromise loco-regional control. This delay can be avoided by starting radiotherapy concurrent with the docetaxel. We evaluated the feasibility of concurrent docetaxel and radiation therapy to chest wall and peripheral lymphatics after four cycles of AC chemotherapy. The preliminary results were reported in ASCO 2005 (Abstract 858). Methods: Females between 18–50 years, T2-T3 lesions, four or more positive nodes and hormone receptor negative tumors were eligible. Patients were enrolled after MRM. Four cycles of AC at 60/600 mg/m2 were followed by four cycles of docetaxel at 75mg/m2 every 21-days. Concurrent radiation to chest wall and peripheral lymphatics was started with the third cycle of docetaxel. A dose of 50 Gy in 5 weeks or equivalent was delivered. Successful completion of treatment in 18 out of 20 or 25 out of 30 patients was chosen as an index of feasibility. CTC version 2.0 of NCI and RTOG/EORTC Late Radiation Morbidity Scoring Scheme was used. Results: All the 30 enrolled patients successfully completed the planned treatment. Radiation was completed within 6 months of surgery in 27(90%) of the patients. Febrile neutropenia was seen in 5(16.7%). Grade-3 neutropenia and diarrhea in 8(26.7%) and 6(20%) respectively. Grade-3 dermatitis in the radiated area was seen in 2(6.7%) and grade-2 in 5(16.7%). Late toxicity included grade-2 skin atrophy and telangiectasia in radiated area in 6(20%) each. At a median follow up of 20 months (range 9–25 months) two local recurrences and two systemic relapses have been seen. Conclusion: This treatment schedule is feasible and safe in patients with high-risk operable breast cancer. It allows delivery of post mastectomy radiation within 6 months of surgery in patients undergoing sequential AC-docetaxel chemotherapy. No significant financial relationships to disclose.


2006 ◽  
Vol 9 (S1) ◽  
pp. 332-339
Author(s):  

This section provides current contact details and a summary of recent or ongoing clinical trials being coordinated by Japan Breast Cancer Research Group (JBCRG). Clinical trials include: Study of CEF-DOC as primary systemic chemotherapy for operable breast cancer.Study of FEC-DOC100 as primary systemic chemotherapy for operable breast cancer.DOC-FEC as primary systemic chemotherapy.


2004 ◽  
Vol 71 (3) ◽  
pp. 281-285 ◽  
Author(s):  
Ian S Fentiman ◽  
Vinay Deshmane ◽  
David Tong ◽  
John Winter ◽  
Helen Mayles ◽  
...  

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