Nonrandomized Comparison between Concomitant and Sequential Chemoradiotherapy with Anthracyclines in Breast Cancer

Author:

Leonardi Maria Cristina1,Morra Anna1,Santoro Luigi2,Balduzzi Alessandra3,Ivaldi Giovanni Battista4,Vischioni Barbara5,Ferrari Annamaria1,Fodor Cristiana1,Dell'Acqua Veronica1,Cardinale Daniela Maria6,Cipolla Carlo6,Luini Alberto7,Colleoni Marco3,Jereczek-Fossa Barbara Alicja18,Orecchia Roberto18

Affiliation:

1. Division of Radiotherapy, European Institute of Oncology, Milan - Italy

2. Division of Epidemiology and Biostatistics, European Institute of Oncology, Milan - Italy

3. Research Unit in Medical Senology, Department of Medicine, European Institute of Oncology, Milan - Italy

4. Department of Radiation Oncology, Maugeri Foundation, Pavia - Italy

5. National Centre for Hadron Therapy (CNAO), Pavia - Italy

6. Division of Cardiology, European Institute of Oncology, Milan - Italy

7. Division of Senology, European Institute of Oncology, Milan - Italy

8. University of Milan, Milan - Italy

Abstract

Purpose To evaluate the tolerance of concomitant administration of anthracycline-based chemotherapy (CHT) and 3-dimensional conformal radiotherapy (RT) after breast-conserving surgery. Methods and Materials Sixty-seven patients, treated with conservative surgery followed by 3-dimensional whole breast RT and concomitant CHT regimens including “Canadian modified” CEF (5-fluorouracil, epirubicin, cyclophosphamide) or AC (doxorubicin, cyclophosphamide) were evaluated for toxicity. They were compared in terms in compliance and acute toxicity with 67 patients irradiated sequentially after having received anthracyclines. Results Acute grade ≥2 skin toxicity was significantly higher in the concomitant group compared to the sequential group, although the incidence of Grade 3 desquamation showed no statistical difference (9% vs. 3%, p = 0.14). Haematological toxicity represented the main cause of treatment discontinuation, reporting higher rate of grade 3-4 leuco-neutropenia in the concomitant group (20.9% vs. 6%, p = 0.01). Mean RT duration was longer in the concomitant group (51 days vs. 45 days) owing to RT breaks. Late toxicity was acceptable. No symptomatic lung and heart events were reported. Radiological lung hyperdensity was detected in 27.7% of the patients in the concomitant group. Post-treatment left ventricular ejection fraction significantly decreased compared with baseline, but cardiac function remained within the normal range, without any difference between left or right-sided RT. Conclusions Although there was more acute grade ≥2 skin toxicity in the concomitant group, the rate of grade 3 dermatitis was lower than expected, suggesting some advantages of 3-D CRT over older techniques. Haematological toxicity exerted a significant impact on both RT and CHT delivery.

Publisher

SAGE Publications

Subject

Cancer Research,Oncology,General Medicine

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