2014, Número 3
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Rev Mex Mastol 2014; 4 (3)
Análisis de la efectividad de epirrubicina neoadyuvante de alta dosis al usar 4 vs. 6 ciclos en pacientes con cáncer de mama localmente avanzado
Ramírez-Torres N, Pérez-Puentes A, Astudillo-de la Vega H
Idioma: Español
Referencias bibliográficas: 43
Paginas: 91-99
Archivo PDF: 329.54 Kb.
RESUMEN
Propósito: Agentes citostáticos como las antraciclinas han demostrado ser eficaces en el tratamiento del cáncer de mama localmente avanzado (CMLA). La epirrubicina puede utilizarse en dosis altas sin incrementar la toxicidad severa. Nuestro objetivo fue evaluar la dosis alta de epirrubicina al usar 4 vs. 6 ciclos.
Pacientes y métodos: Pacientes diagnosticadas con CMLA se incluyeron en nuestro hospital. Una cohorte (n = 48) recibió 5-fluorouracilo 500 mg/m
2, epirrubicina 100 mg/m
2 y ciclofosfamida 600 mg/m
2 (FE
100C) por cuatro ciclos (4FE
100C). Otra cohorte (n = 48) recibió seis ciclos del mismo esquema (6FE
100C). A todas las pacientes se les realizó cirugía, radioterapia y quimioterapia adyuvante.
Resultados: Se obtuvo una tasa significativa de respuesta objetiva (RO) de 87.5% para 6FE100C frente al 62.5% para 4FE
100C (p ‹ 0.004). Al aumentar el número de ciclos administrados (6FE
100C) hubo una mejora no significativa en las tasas de respuesta patológica completa (RPc) (20.8%; p = 0.273) y de ganglios negativos postquimioterapia (37.5%; p = 0.960). La toxicidad predominante para 6FE
100C fue vómito (52.4%; p = 0.001) y náusea (91.6%; p = .563), ambos con grado 1-2. La
odds ratio indicó que el uso de 6FE
100C comparado con 4FE
100C incrementó 1.6 veces la posibilidad de RPc y la dosis intensiva de epirrubicina fue el factor controlable más importante para determinar la RPc sin incrementar la toxicidad severa.
Conclusión: El beneficio de la respuesta clínica y patológica fue mejor para el tratamiento prolongado de seis ciclos al usar una dosis alta de epirrubicina.
REFERENCIAS (EN ESTE ARTÍCULO)
De Lena M, Varini M, Zucali R et al. Multimodality treatment for locally advanced breast cancer. Cancer Clin Trials. 1981; 4: 229-236.
Tranum BL, McDonald B, Thigpen T et al. Adriamycin combinations in advanced breast cancer. A Southwest Oncology Group Study. Cancer. 1982; 49: 835-839.
Hortobagyi GN, Ames FC, Buzdar AU. Management of stage III primary breast cancer with primary chemotherapy, surgery and radiation therapy. Cancer. 1988; 62: 2507-2516.
Italian Multicentre Breast Study with epirubicin. Phase III randomized study of fluorouracil, epirubicin and cyclophosphamide vs. fluorouracil, doxorubicin and cyclophosphamide in advanced breast cancer: an Italian multicentre trial. J Clin Oncol. 1988; 6: 976-982.
French Epirubicin Study Group. A prospective randomized phase III trial comparing combination chemotherapy with cyclophosphamide, fluorouracil and either doxorubicin or epirubicin. J Clin Oncol. 1988; 6: 679-688.
Fisher B, Brown AM, Mamounas E et al. Effect of preoperative chemotherapy on local-regional disease in women with operable breast cancer: findings from National Surgical Adjuvant Breast Project B-18. J Clin Oncol. 1997; 15: 2483-2493.
Mouret-Reynier MA, Abrial CJ, Ferriere JP et al. Neoadjuvant FEC100 for operable breast cancer: eight-year experience at Centre Jean Perrin. Clin Breast Cancer. 2004; 5: 303-307.
Shenkier T, Weir L, Levine M et al. Clinical practice guidelines for the care and treatment of breast cancer: 15. Treatment for women with stage III or locally advanced breast cancer. CMAJ. 2004; 170: 983-994.
Sachelarie I, Grossbard ML, Chadha M et al. Primary systemic therapy of breast cancer. The Oncologist. 2006; 11: 574-589.
Jacquillat C, Baillet F, Weil M et al. Results of a conservative treatment combining induction (neoadjuvant) and consolidation chemotherapy, hormonotherapy and external irradiation and interstitial irradiation in 98 patients with locally advanced breast cancer (IIIA-IIIB). Cancer. 1988; 61: 1977-1982.
Cocconi G, di Blasio B, Bisagni G et al. Neoadjuvant chemotherapy and endocrine therapy in locally advanced breast carcinoma. A prospective randomised study. Am J Oncol. 1990; 13: 226-232.
Feldman DL, Hortobagyi GN, Buzdar AU et al. Pathologic assessment of response to induction chemotherapy in breast cancer. Cancer Res. 1986; 46: 2578-2581.
Jacquillat C, Weil M, Baillet F et al. Results of the neoadjuvant chemotherapy, and external and radiation therapy in breast-conserving treatment of 250 patients with all stages of infiltrative breast cancer. Cancer. 1990; 66: 119-129.
Calais G, Berger C, Descamps P et al. Conservative treatment feasibility with induction chemotherapy, surgery and radiotherapy for patients with breast carcinoma larger than 3 cm. Cancer. 1994; 74: 1283-1288.
Torti FM, Bristol MM, Lum BL et al. Cardiotoxicity of epirubicin and doxorubicin: assessment by endomyocardial biopsy. Cancer Res. 1986; 46: 3722-3727.
Ryberg M, Nielsen D, Skovsgaard T et al. Epirubicin cardiotoxicity: an analysis of 469 patients with metastatic breast cancer. J Clin Oncol. 1998; 6: 3502-3508.
French Epirubicin Study Group. A prospective trial comparing epirubicin monochemotherapy to two fluorouracil, cyclophosphamide and epirubicin regimens differing in epirubicin dose in advanced breast cancer patients. J Clin Oncol. 1991; 9: 305-312.
Focan C, Andrien JM, Closon MT et al. Dose-response relationship of epirubicin based first-line chemotherapy for advanced breast cancer: a prospective randomised trial. J Clin Oncol. 1993; 11: 1253-1263.
Bastit P, Roche H, Namer M et al. Final results of a randomized trial comparing three epirubicin based regimens as first line chemotherapy in metastatic breast cancer (MBC) patients (PTS). Proc Am Soc Clin Oncol. 1999; 18: 128 (Abstr 487).
French Epirubicin Study Group. Epirubicin-based chemotherapy in metastatic breast cancer patients: role of dose-intensity and duration of treatment. J Clin Oncol. 2000; 18: 3115-3124.
Singletary SE, Alfred C, Ashley P et al. Revision of the American Joint Committee on Cancer staging system for breast cancer. J Clin Oncol. 2002; 20: 3628-3636.
Karnorfsky DA, Abelman WH, Craver LF et al. The use of nitrogen mustards in the palliative treatment of cancer. Cancer. 1948; 1: 634-645.
Miller AB, Hoogstraten B, Staquet et al. Reporting results of cancer treatment. Cancer. 1981; 47: 207-214.
Chevallier B, Roche H, Olivier JP et al. Inflammatory breast cancer. Pilot study of intensive induction chemotherapy (FEC-HD) results in a high histologic response rate. Am J Clin Oncol. 1993; 16: 223-228.
Bonadonna G, Valagussa P, Brambilla C et al. Primary chemotherapy in operable breast cancer: eight-year experience at the Milan Cancer Institute. J Clin Oncol. 1998; 16: 93-100.
Broët P, Scholl SM, de la Rochefordière A et al. Short and long term effects on survival in breast cancer patients treated by primary chemotherapy: updated analysis of a randomised trial. Br Cancer Res Treat. 1999; 58: 151-156.
Early Breast Cancer Trialists’ Collaborative Group. Polychemotherapy for early breast cancer: an overview of the randomised trials. Lancet. 1998; 352: 930-942.
Bonneterre J, Roche H, Kerbrat P et al. Epirubicin 100 mg/m2 increases long-term survival in adjuvant chemotherapy of patients with poor-prognosis, node-positive, early breast cancer: 10-year follow-up results of French Adjuvant Study Group 05 randomized trial. J Clin Oncol. 2005; 23: 2686-2693.
Kuerer HM, Newman LA, Smith TL et al. Clinical course of breast cancer patients with complete pathologic primary tumor and axillary lymph node response to doxorubicin-based neoadjuvant chemotherapy. J Clin Oncol. 1999; 17: 460-469.
van der Hage JA, van de Velde CJ et al. Preoperative chemotherapy in primary operable breast cancer: nine-year results from the European Organization for Research and Treatment on Cancer trial 10902. J Clin Oncol. 2001; 19: 4224-4237.
Dieras V, Fumoleau P, Romieu G et al. Randomized parallel study of doxorubicin plus paclitaxel and doxorubicin plus cyclophosphamide as neoadjuvant therapy in patients with breast cancer. J Clin Oncol. 2004; 22: 4958-4965.
Chollet P, Amat S, Cure H et al. Prognostic significance of a complete pathological response after induction chemotherapy in operable breast cancer. Br J Cancer. 2002; 86: 1041-1046.
Luporsi E, Vanlemmens L, Coudert et al. 6 cycles of FEC vs. 6 cycles of epirubicin-docetaxel as neoadjuvant chemotherapy in operable breast cancer patients: preliminary results of a randomized phase II trial of Girec S01 (abstract). Proc Am Soc Clin Oncol. 2000; 19: 92a, 355.
Camaggi CM, Comparsi R, Strocchi E et al. Epirubicin and doxorubicin comparative metabolism and pharmacokinetics. A cross-over study. Cancer Chemother Pharmacol. 1988; 21: 221-228.
Colajori E, Tosello C, Pannuit F et al. Randomized multinational trial comparing epirubicin 50 mg/m2 vs. 100 mg/m2 in combination with 5-fluorouracil and cyclophosphamide as front line treatment of metastatic breast cancer. Ann Oncol. 1994; 5: s3023.
Brufman G, Colajori E, Ghilezan N et al. Doubling epirubicin dose intensity (100 mg/m2 versus 50 mg/m2) in the FEC regimen significantly increases response rates. An international randomized phase III study in metastatic breast cancer. The Epirubicin High Dose (HEPI 010) Study group. Ann Oncol. 1997; 8: 155-162.
Camaggi CM, Strocchi E, Carisi P et al. Epirubicin metabolism and pharmacokinetics after conventional-and high-dose intravenous administration: a cross-over study. Cancer Chemother Pharmacol. 1993; 32: 301-309.
Bastholt L, Dalmark M, Gjedde SB et al. Dose-response relationship of epirubicin in the treatment of postmenopausal patients with metastatic breast cancer: a randomized study of epirubicin at four different dose levels performed by the Danish Breast Cancer Cooperative Group. J Clin Oncol. 1996; 14: 1146-1155.
Therasse P, Mauriac L, Welnicka-Jaskiewicz M et al. Final results of a randomized phase III trial comparing cyclophosphamide, epirubicin and fluorouracil with a dose-intensified epirubicin and cyclophosphamide plus filgrastim as neoadjuvant treatment in locally advanced breast cancer: an EORT-NCIC-SAKK multicenter study. J Clin Oncol. 2003; 21: 843-850.
Velasco-Pérez F, Del Río-González L, Aldaco-Sarvide F et al. Comparación en eficacia y toxicidad del esquema FEC75 vs. FEC100 (fluorouracilo, epirrubicina y ciclofosfamida) como neoadyuvancia en pacientes con cáncer de mama localmente avanzado. Estudio retrospectivo en el Centro Médico Nacional “20 de Noviembre”, ISSSTE. GAMO. 2008; 7 (5): 174-178.
Levine MN, Bramwell VH, Pritchard KI et al. Randomized trial of intensive cyclophosphamide, epirubicin and fluorouracil chemotherapy compared with cyclophosphamide, methotrexate and fluorouracil in premenopausal women with node-positive breast cancer. National Cancer Institute of Canada Clinical Trials Group. J Clin Oncol. 1998; 16: 2651-2658.
Fumoleau P, Kerbrat P, Romestaing P et al. Randomized trial comparing six versus three cycles of epirubicin based adjuvant chemotherapy in premenopausal node-positive breast cancer patients: 10-year follow-up results of the French Adjuvant Study Group 01 trial. J Clin Oncol. 2003; 21: 298-305.
Martin M, Villar A, Sole-Calvo A et al. Doxorubicin in combination with fluorouracil and cyclophosphamide (i.v. FAC regimen, day 1, 21) versus methotrexate in combination with fluorouracil and cyclophosphamide (i.v. CMF regimen, day 1, 21) as adjuvant chemotherapy for operable breast cancer: a study by the GEICAM group. Ann Oncol. 2003; 14: 833-842.