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Postmenopausal Metastatic Breast Cancer

A Review of First-Line Treatment Options

  • Review Article
  • Published:
American Journal of Cancer

Abstract

Endocrine therapy and chemotherapy play important roles in the management of postmenopausal women with metastatic breast cancer. This paper specifically reviews the indications and options for first-line treatment of metastatic breast cancer and recent advances are highlighted, with particular attention to randomized, controlled, phase III clinical trials.

Until recently, tamoxifen was standard first-line endocrine treatment for patients with metastatic breast cancer. Now, potent third generation aromatase inhibitors, such as letrozole and anastrozole, have shown superiority to tamoxifen as first-line endocrine treatment and provide an alternative for postmenopausal women.

The most active chemotherapy agents for patients with advanced breast cancer have, until recently, been the anthracyclines, doxorubicin and epirubicin. However, their increasing use in the adjuvant setting has resulted in a need for novel active non-cross-resistant cytotoxic drugs for metastatic breast cancer. Real progress has been made with the introduction of the taxanes, paclitaxel and docetaxel. Other developments include the use of single agent cytotoxics such as vinorelbine, the oral fluoropyrimidine capecitabine and gemcitabine, all of which have some activity following either taxanes or anthracyclines, along with a low toxicity profile. Bisphosphonates are bone-specific palliative treatments that have been instituted on the basis of their impact on symptoms and skeletal related morbidity.

Finally, the era of biological therapy in the clinic for patients with breast cancer has been heralded with the development and introduction of trastuzumab, a humanized monoclonal antibody which targets the cell surface growth factor receptor HER2/neu. Importantly, each of these new treatment options has provided an incremental improvement in efficacy over previous standard first-line therapies.

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References

  1. Office for National Statistics. Mortality statistics: review of the Register General on deaths by sex and age, England and Wales, 1999. London: The Stationery Office, 2000

    Google Scholar 

  2. Cancer Research Campaign. Cancer Research Campaign, CRC Cancer Stats; Mortality UK, London. Available from URL: http://www.crc.org.uk/cancer/pageimages/csmortality.pdf [Accessed 2002 Jul 19]

  3. Greenberg P, Hortobagyi G, Smith T, et al. Long-term follow-up of patients with complete remission following combination chemotherapy for metastatic breast cancer. J Clin Oncol 1996; 14: 2197–205

    PubMed  CAS  Google Scholar 

  4. Early Breast Cancer Trialists’ Collaborative Group. Polychemotherapy for early breast cancer: an overview of the randomised trials. Lancet 1998; 352: 930–42

    Article  Google Scholar 

  5. Early Breast Cancer Trialists’ Collaborative Group. Tamoxifen for early breast cancer: an overview of the randomised trials. Lancet 1998; 351: 1451–67

    Article  Google Scholar 

  6. Rubens R, Bajetta E, Bonneterre J, et al. Treatment of relapse of breast cancer after adjuvant systemic therapy. Eur J Cancer 1994; 30A: 106–11

    Article  PubMed  CAS  Google Scholar 

  7. Encarnacion C, Ciocca D, McGuire W, et al. Measurement of steroid hormone receptors in breast cancer patients on tamoxifen. Breast Cancer Res Treat 1993; 26: 237–46

    Article  PubMed  CAS  Google Scholar 

  8. Johnston SR, Saccani Totti G, Smith IE, et al. Changes in estrogen receptor, progesterone receptor, and pS2 expression in tamoxifen-resistant human breast cancer. Cancer Res 1995; 55(15): 3331–8

    PubMed  CAS  Google Scholar 

  9. Goldhirsch A. Breast cancer. In: Cavalli F. Hansen H. Kaye S, editors. Textbook of medical oncology. London: Martin Dunitz, 1997: 53–87

    Google Scholar 

  10. Johnston SRD. Acquired tamoxifen resistance in human breast cancer: potential mechanisms and clinical implications. Anticancer Drugs 1997; 8(10): 911–30

    Article  PubMed  CAS  Google Scholar 

  11. Howell A, DeFriend D, Robertson J, et al. Response to a specific antioestrogen (ICI 182780) in tamoxifen-resistant breast cancer. Lancet 1995; 345: 29–30

    Article  PubMed  CAS  Google Scholar 

  12. Howell A, Robertson JRF, Albano J, et al. Fuivestrant is as effective as anastrozoie in post-menopausal women with advanced breast cancerprogressing after prior treatment. J Clin Oncol 2002; 16: 3396–402

    Article  Google Scholar 

  13. Osbourne CK, Pippen J, Jones SE, et al. Double-blind randomized trial comparing the efficacy and tolerability of fuivestrant versus anastrozole in post-menopausal women with advanced breast cancer progressing after prior endocrine therapy. J Clin Oncol 2002; 16: 3386–95

    Article  Google Scholar 

  14. Johnston S. Endocrine manipulation in advanced breast cancer: recent advances with SERM therapies. Clin Cancer Res 2001; 7Suppl. 1: 4376s–87s

    PubMed  CAS  Google Scholar 

  15. Gradishar W, Giusman J, Vogel C, et al. Raloxifene HCL, a new endocrine agent, is active in estrogen receptor positive (ER+) metastatic breast cancer. Breast Cancer Res Treat 1997; 46: 53

    Google Scholar 

  16. Curnrnings S, Eckert S, Krueger K, et al. The effect of raloxifene on risk of breast cancer in posmtenopausal women: results from the multiple outcomes of raloxifene evaluation (MORE) randomized trial. JAMA 1999; 281: 2189–97

    Article  Google Scholar 

  17. Fisher B, Costantino J, Wickerham D, et al. Tamoxifen for prevention of breast cancer: report of the National Surgical Adjuvant Breast and Bowel Project P-1 study. J Natl Cancer Inst 1998; 90(18): 1371–88

    Article  PubMed  CAS  Google Scholar 

  18. Brodie A, Njar V. Aromatase inhibitors and breast cancer. Semin Oncol 1996; 23(4 Suppl. 9): 10–20

    PubMed  CAS  Google Scholar 

  19. Miller WR. Aromatase inhibitors. Endocr Relat Cancer 1996; 3(1): 65–79

    Article  CAS  Google Scholar 

  20. Geisler J, Haynes B, Anker G, et al. Influence of letrozoie and anastrozole on total body arorealization and plasma estrogen levels in postmenopausal breast cancer patients evaluated in a randomized, cross-over study. J Clin Oncol 2002: 20; 751–57

    Article  PubMed  CAS  Google Scholar 

  21. Buzdar A, Jonat W, Howell A, et al. Anastrozole, a potent and selective aromatase inhibitor, versus megestrol acetate in post-menopausal women with advanced breast cancer: results of overview analysis of 2 phase III trials. J Clin Oncol 1996; 14: 2000–11

    PubMed  CAS  Google Scholar 

  22. Buzdar A, Jonat W, Howell A, et al. Anastrozoie vs megestrol acetate in the treatment of postmsnopausal women with advanced breast carcinoma: results of a survival update based on a combined analysis of data from two mature phase III trials. Cancer 1998; 83: 1142–52

    Article  PubMed  CAS  Google Scholar 

  23. Dombernowsky P, Smith I, Falkson G, et al. Letrozoie, a new oral aromatase inhibitor for advanced breast cancer: doubie-blind randomized trial showing a dose effect and improved efficacy and tolerability compared with megestrol acetate. J Clin Oncol 1998; 16(2): 453–61

    PubMed  CAS  Google Scholar 

  24. Buzdar A, Douma J, Davidson N, et al. Phase III, multicenter, double-blind, randomized study of letrozole, an aromatase inhibitor, for advanced breast cancer versus megestrol acetate. J Clin Oncol 2001; 19(14): 3357–66

    PubMed  CAS  Google Scholar 

  25. Kvinnsiand S, Anker G, Dirix L, et al. High activity and tolerability demonstrated for exemestane in postmenopausai women with metastatic breast cancer who had previously failed on tamoxifen treatment. Eur J Cancer 2000; 36: 976–82

    Article  Google Scholar 

  26. Lonning P, Bajetta E, Murray R, et al. Activity of exemestane in metastatic breast cancer after failure of nonsteroidal aromatase inhibitors: a phase II trial. J Clin Oncol 2000; 18(11): 2234–44

    PubMed  CAS  Google Scholar 

  27. Thurlimann B, Paridaens R, Serin D, et al. Third-line hormonal treatment with exemestane in postmenopausai patients with advanced breast cancer progressing on aminogiutethimide: a phase II multicentre multinational study: Exemestane Study Group. Eur J Cancer 1997; 33(11): 1767–73

    Article  PubMed  CAS  Google Scholar 

  28. Kaufmann M, Bajetta E, Dirix L, et al. Exemestane is superior to megestrol acetate after tamoxifen failure in postmenopausai women with advanced breast cancer: results of a phase III randomized double-blind trial. J Clin Oncol 2000; 18(7): 1399–411

    PubMed  CAS  Google Scholar 

  29. Nabhoitz J, Buzdar A, Pollak M, et al. Anastrozole is superior to tamoxifen as first-line therapy for advanced breast cancer in postraenopausal women: results of a North American multicenter randomized trial. J Clin Oncol 2000; 18(22): 3758–67

    Google Scholar 

  30. Bonneterre J, Thurlimann B, Robertson J, et al. Anastrozoie versus tamoxifen as first-line therapy for advanced breast cancer in 668 postmenopausal women: results of the tamoxifen or Arimidex randomized group efficacy and tolerability study. J Clin Oncol 2000; 18(22): 3748–57

    PubMed  CAS  Google Scholar 

  31. Mouridsen H, Gershanovich M, Sun Y, et al. Superior efficacy of letrozoie versus tamoxifen as first-line therapy for postmenopausai women with advanced breast cancer: results of a phase III study of the International Letrozoie Breast Cancer Group. J Clin Oncol 2001; 19(10): 2596–606

    PubMed  CAS  Google Scholar 

  32. Dirix L, Piccart M, Lohrisch C, et al. Efficacy of and tolerance to exemestane versus tamoxifen in first line hormone therapy of postmenopausal metastatic breast cancer patients: a European Organisation for the Research and Treatment of cancer (EORTC Breast Group) Phase II trial with Pharmacia and Upjohn. Proc Am Soc Clin Oncol 2001; 20: 114a

    Google Scholar 

  33. Buzdar A, Nabhoitz J, Robertson J, et al. Anastrozole (Arimidex) versus tamoxifeu as first-line therapy for advanced breast cancer (ABC) in postmenopausal (PM) women — combined analysis from two identically designed multicenter trials [abstract 609D]. Proc Am Soc Clin Oncol 2000; 19: 154A

    Google Scholar 

  34. ATAC Trialists’ Group. Anastrozole alone or in combination with tamoxifen versus tamoxifen alone for adjuvant treatment of postmenopausal women with early breast cancer: first results of the ATAC Randomised Trial. Lancet 2002; 359: 2131–9

    Article  Google Scholar 

  35. Cold S, Jensen N, Brincker H. The influence of chemotherapy on survival after recurrence in breast cancer: a population based study of patients treated in the 1950s, 1960s, and 1970s. Eur J Cancer 1993; 29: 1146–52

    Article  Google Scholar 

  36. Geels P, Eisenhauer E, Bezjak A, et al. Palliative effect of chemotherapy: objective tumor response is associated with symptom improvement in patients with metastatic breast cancer. J Clin Oncol 2000; 18(12): 2395–405

    PubMed  CAS  Google Scholar 

  37. Falkson G, Gelman R, Glick J, et al. Metastatie breast cancer: higher versus low dose maintenance treatment when only a partial response or a no change status is obtained following doxorubicin induction treatment: an Eastern Cooperative Oncology Group study. Ann Oncol 1992; 3(9): 768–70

    PubMed  CAS  Google Scholar 

  38. Falkson G, Gelman R, Pandya K, et al. Eastern Cooperative Oncology Group randomized trials of observation versus maintenance therapy for patients with metastatic breast cancer in complete remission following induction treatment. J Clin Oncol 1998; 16(5): 1669–76

    PubMed  CAS  Google Scholar 

  39. Muss EL, Case L, Richards II F, et al. Interrupted versus continuous chemotherapy in patients with metastatic breast cancer. N Engl J Med 1991; 325(19): 1342–8

    Article  PubMed  CAS  Google Scholar 

  40. Perez E. Current management of metastatic breast cancer. Semin Oncol 1999; 26(4 Suppl. 12): 1–10

    PubMed  CAS  Google Scholar 

  41. Camaggi C, Strocchi E, Carisi P. Epirubicin metabolism and pharmacokinetics after conventional- and high-dose intravenous administration: a cross-over study. Cancer Chemother Pharmacol 1993; 32: 301–9

    Article  PubMed  CAS  Google Scholar 

  42. French Epirubicin Study Group. A prospective randomized phase III trial comparing combination chemotherapy with cyclophosphamide, fluorouracil and with either doxorubicin or epirubicin. J Clin Oncol 1988; 6: 679–88

    Google Scholar 

  43. French Epirubicin Study Group. A prospective randomized trial comparing epirubicin monochemotherapy to two fluorouracil, cylophosphamide, and epirubicin regimens differing in epirubicin dose in advanced breast cancer patients. J Clin Oncol 1991; 9: 305–12

    Google Scholar 

  44. Biganzoli L, Piccart M. The bigger the better? Or what we know and what we still need to learn about anthracycline dose per course, dose density and cumulative dose in the treatment of breast cancer. Ann Oncol 1997; 8: 1177–82

    Article  PubMed  CAS  Google Scholar 

  45. Buzdar A, Hortobagyi G, Prye D, et al. Second-line chemotherapy for metastatic breast cancer including quality of life issues. Breast 1996; 5: 312–7

    Article  Google Scholar 

  46. Sjostrom J, Biomqvist C, Mouridsen H, et al. Docetaxei compared with sequential methotrexate and 5-fluorouracil in advanced breast cancer after anthracycline failure: a randomised phase III study with cross-over on progression by the Scandinavian Breast Cancer Group. Eur J Cancer 1999; 35: 1194–201

    Article  PubMed  CAS  Google Scholar 

  47. Nabholtz J, Senn J, Beswoda W, et al. Prospective randomised trial of docetaxel vs mitomycin plus vinbiastine in patients with metastatic breast cancer progressing despite previous anthracyciine-containing chemotherapy. J Clin Oncol 1999; 17: 1413–24

    PubMed  CAS  Google Scholar 

  48. Bonneterre J, Roche H, Monnier A, et al. Taxoiere vs 5-FU and Naveibine as second-line chemotherapy in patients wiith metastatic breast cancer. Proc Am Soc Clin Oncol 1997; 16: A564

    Google Scholar 

  49. Chan S, Friedrichs K, Noel D, et al. Prospective randomised phase III triai of docetaxel vs doxorubicin in patients with metastatic breast cancer. J Clin Oncol 1999; E7: 2341–54

    Google Scholar 

  50. Sledge GW, Neuberg D, Bernando P, et al. Phase III trial of doxorubicin vs paclitaxel vs doxorabicin + paclitaxel as front-line chemotherapy for metastatic breast cancer; an intergroup trial [abstract]. J Clin Oncol 2003; 21: 588–92

    Article  PubMed  Google Scholar 

  51. Paridaens R, Biganzoli L, Broiling P, et al. Paclitaxel vs doxorabicin as first-line single agent chemotherapy for metastatic breast cancer; a European Organisation for Research and Treatment of Cancer randomised study with cross-over. J Clin Oncol 2000; 18: 724–33

    PubMed  CAS  Google Scholar 

  52. Bishop J, Dewar J, Toner G, et al. Initial paclitaxel improves outcome compared with CMFP combination chemotherapy as front-line therapy in untreated metastatic breast cancer. J Clin Oncol 1999; 17: 2355–64

    PubMed  CAS  Google Scholar 

  53. Perez EA, Vogel CL, Irwin DH, Krishner JJ, Patel R. Multicenter Phase II trial of weekly paclitaxel in women with metastatic breast cancer. J Clin Oncol 2001; 18: 4216–33

    Google Scholar 

  54. Burstein EL, Manola J, Younger J, et al. Docetaxel administered on a weekly basis for metastatic breast cancer. J Clin Oncol 2000; 19: 1212–9

    Google Scholar 

  55. Tassera J. Pienkowski T, Pluzanska A, et al. Doxorabicin and paclitaxel versus fluorouracil, doxorabicin, and cyclophopsharnide as first-line therapy for women with metastatic breast cancer: final results of a randomized phase III multicenter trial. J Clin Oncol 2001; 19(6): 1707–15

    Google Scholar 

  56. Biganzoli L, Cufer T, Braning P, et al. Doxorubicin and paclitaxel versus doxorabicin and cyclophosphamide as first line chemtoherapy in metastatic breast cancer: the European Organisation for Research and Treatment of cancer 10961 multicenter phase III trial. J Clin Oncol 2002; 20: 3114–21

    Article  PubMed  CAS  Google Scholar 

  57. Luck EL, Thomssen C, Untch M, et al. Multicentric phase III study in first line treatment of advanced metastatic breast cancer (ABC): epirubicin/paclitaxel (ET) vs epirubicin/cyclophosphamide (EC) — a study of the AGO Breast Cancer Group. Proc Am Soc Clin Oncol 2000; 19: 73A

    Google Scholar 

  58. Carmichael J. UKCCR trial of epirubicin and cyclophosphamide vs epirubicin and taxolin the first line treamtnet of women with metastatic breast cancer [abstract 84a]. Proc Am Soc Clin Oncol 2001; 20: 22

    Google Scholar 

  59. Nabhoitz J-M, Falkson G, Campos D, et al. Doccetexal and doxorubicin compared with doxorubicin and cyclophosphamide as first-line chemotherapy for metastatic breast caner; results of a randomised, multicenter phase III triai. J Clin Oncol 2003; 21: 968–75

    Article  Google Scholar 

  60. Mackey J, Paterson A, Dirix L, et al. Final results of the phase III randomized trial comparing docetaxel (T), doxorabicin (A) and cyclophosphamide (C) to FAC as first line chemotherapy for patients with metastatic breast cancer [abstract 137]. Proc Am Soc Clin Oncol 2002; 21: 35a

    Google Scholar 

  61. Sparano J, O’Neill A, Schaefer P, et al. Phase II trial of doxorabicin and docetaxel plus granuiocyte colony-stimuitating factor in metastatic breast cancer: Eastern Cooperative Oncology Group Study E1196. J Clin Oncol 2000; 18: 2369–77

    PubMed  CAS  Google Scholar 

  62. Sparano J, Hu P, Rao R, et al. Phase II trial of doxorubicn and paclitaxel pius granuiocyte colony-stimulating factor in metastatic breast cancer: an Eastern Cooperative Oncology Group Study. J Clin Oncol 1999; 17: 3828–34

    PubMed  CAS  Google Scholar 

  63. Gianni L, Munzone E, Capri G, et al. Paclitaxel by 3-hour infusion in combination with bolus doxorabicin in women with untreated metastatic breast cancer: high antiturnor efficacy and cardiac effects in a dose-finding and sequence-finding study. J Clin Oncol 1995; 13(11): 2688–99

    PubMed  CAS  Google Scholar 

  64. Nabholtz J, Pienkowski T, Mackey J, et al. Phase III trial comparing TAC (docetaxel, doxorabicin, cyclophosphamide) with FAC (5-fluorouracil, doxorabicin, cyclophosphamide) in the adjuvant treatment of node positive breast cancer aptients: interim analysis of the BCIRG 001 study [abstract 141]. Proc Am Soc Clin Oncol 2002; 21: 36a

    Google Scholar 

  65. Buzdar AU, Singletary SE, Valero V, et al. Evaluation of paclitaxel in adjuvant chemotherapy for patients with operable breast cancer; preliminary results of a prospective randomised trial. Clin Cancer Res 2002; 8: 1073–9

    PubMed  CAS  Google Scholar 

  66. Blum J, Jones S, Buzdar A, et al. Multicenter phase II study of capecitabine in paclitaxel-refractory metastatic breast cancer. J Clin Oncol 1999; 17: 485–93

    PubMed  CAS  Google Scholar 

  67. O’Shaughnessy J, Blum J, Moiseyenko V, et al. Randomized, open-label, phase II trial of oral capecitabine (Xeloda) vs a reference arm of intravenous CMF (cyclophosphamide, methotrexate and 5-fluorouracil) as first line therapy for advanced/metastatic breast cancer. Ann Oncol 2001; 12(9): 1247–54

    Article  Google Scholar 

  68. Engelsman E, Klijn J, Rubens R, et al. “Classical” CMF versus a 3-weekly intravenous CMF schedule in postmen op ausal patients with advanced breast cancer: an EORTC Breast Cancer Co-Operative Group Phase III Trial (10808). Eur J Cancer 1991; 27(8): 966–70

    Article  PubMed  CAS  Google Scholar 

  69. Fumoleau P, Largillier R, Trillet-Lenoir V, et al. Capecitabine (Xeloda) in patients with advanced breast cancer, previously treated with anthracycline s and taxanes: results of a large phase II study [abstract 247]. Proc Am Soc Clin Oncol 2002; 21: 62a

    Google Scholar 

  70. Degardin M, Bonneterre J, Hecquet B, et al. Vinorelbine (naveibine) as a salvage treatment for advanced breast cancer. Ann Oncol 1994; 5: 423–6

    PubMed  CAS  Google Scholar 

  71. Marty M, Extra J, Dieras V, et al. A review of the antitumour activity of vinorelbine in breast cancer. Drags 1992; 44Suppl. 4: 29–35

    Article  CAS  Google Scholar 

  72. Jones S, Winer E, Vogel C, et al. Randomized comparison of vinorelbine and melphalan in anthracycline-refractory advanced breast cancer. J Clin Oncol 1995; 13(10): 2567–74

    PubMed  CAS  Google Scholar 

  73. Spielmann M, Kalla S, Llombart-Cussac A, et al. Activity of gemcitabine in metastatic breast cancer patients previously treated with anthracycline-containing regimens. Eur J Cancer 1997; 33Suppl. 8: A663

    Google Scholar 

  74. Brodowicz T, Moslinger R, Herscovici V, et al. Second- and third-line treatent of metastatic breast cancer with gemcitabine. Eur J Cancer 1958; 34Suppl. 5: A180

    Google Scholar 

  75. Rahman Z, Frye D, Buzdar A, et al. Impact of selection process on response rate and long-term survival of potential high-dose chemotherapy candidates treated with standard-dose doxorubicin-containing chemotherapy in patients with metastatic breast cancer. J Clin Oncol 1997; 15: 3171–7

    PubMed  CAS  Google Scholar 

  76. Lotz J, Cure H, Janvier M, et al. High-dose chemotherapy with haemopoietic transplantation for metastatic breast cancer: results of the French protocol PEGASE 04 [abstract 161]. Proc Am Soc Clin Oncol 1999; 18: 43a

    Google Scholar 

  77. Stadtmauer E, O’Neill A, Goldstein L, et al. Conventional-dose chemotherapy compared with high-dose chemotherapy plus autoiogous haematopoetic stem cell transplant group. N Engl J Med 2000; 342: 1069–76

    Article  PubMed  CAS  Google Scholar 

  78. Stadtmauer E, O’Neill A, Goldstein L, et al. Conventional-dose chemotherapy compared with high-dose chemotherapy plus autoiogous stem-cell transplantation for metastatic breast cancer: 5-year update of the “Philadelphia Trial” [abstract 169]. Proc Am Soc Clin Oncol 2002; 21: 43a

    Google Scholar 

  79. Paterson A, Powles T, Kanis J, et al. Double-blind controlled trial of oral clodronate in patients with bone metastases from breast cancer. J Clin Oncol 1993; 11: 59–65

    PubMed  CAS  Google Scholar 

  80. Conte P, Latrielle J, Mauriac L, et al. Delay in progression of bone metastases in breast cancer patients treated with intravenous pamidronate: results from a multinational randomised controlled trial. J Clin Oncol 1996; 14: 2552–9

    PubMed  CAS  Google Scholar 

  81. Hortobagyi G, Theriault R, Porter L, et al. Efficacy of pamidronate in reducing skeletal complications in patients with breast cancer and lytic bone metastases. N Engl J Med 1996; 335: 1785–91

    Article  PubMed  CAS  Google Scholar 

  82. Lipton A, Theriault R, Hortobagyi G, et al. Pamidronate prevents skeletal complications and is effective palliative treatment in women with breast carcinoma and osteolytic bone metastases. Cancer 2000: 88: 1082–90

    Article  PubMed  CAS  Google Scholar 

  83. Theriauit R, Lipton A, Hortobagyi G, et al. Pamidronate reduces skeletal morbidity in women with advanced breast cancer and lytic bone lesions: a randomized, placebo-controlled trial-protocol 18 Aredia Breast Cancer Study Group. J Clin Oncol 1999; 17: 846–54

    Google Scholar 

  84. Breast Specialty Group of the British Association of Surgical Oncology. The management of metastatic bone disease in the United Kingdom. Eur J Surg Oncol 1999; 25: 3–23

    Article  Google Scholar 

  85. Hillner B, Ingle J, Berenson J, et al. American Society of Clinical Oncology guideline on the role of bisphosphonates in breast cancer: American Society of Oncology Bisphosphonates Expert Panel. J Clin Oncol 2000; 18: 1378–91

    PubMed  CAS  Google Scholar 

  86. Diel I, Marschner N, Kindler M, et al. Continual oral versus intravenous interval therapy with bisphosphonates in patients with breast cancer and bone metastases [abstract 488A]. Proc Am Soc Clin Oncol 1999; 18: 128

    Google Scholar 

  87. Slamon DJ, Clark GM, Wong SG, et al. Human breast cancer: correlation of relapse and survival with amplification of the HER-2/neu oncogene. Science 1987; 235(4785): 177–82

    Article  PubMed  CAS  Google Scholar 

  88. Baselga J, Tripathy D, Mendelsohn 3, et al. Phase II study of weekly intravenous recombinant humanized Anti-p185HER2 monoclonal antibody in patients with HER2/neu-overexpressing metastatic breast cancer. J Clin Oncol 1996; 14(3): 737–44

    PubMed  CAS  Google Scholar 

  89. Pegram MD, Lipton A, Hayes DF, et al. Phase II study of receptor-enhanced chernosensitivity using recombinant humanized anti-p185HER2/neu monoclonal antibody plus cisplatin in patients with HER2/neu-overexpressing metastatic breast cancer refractory to chemotherapy treatment. J Clin Oncol 1998; 16(8): 2659–71

    PubMed  CAS  Google Scholar 

  90. Cobleigh M, Vogel C, Tripathy D, et al. Multinational study of the efficacy and safety of humanized anti-HER2 monoclonal antibody in women who have HER2-overexpressiing metastatic breast cancer that has progressai after chemotherapy for metastatic disease. J Clin Oncol 1999; 17(9): 2639–48

    PubMed  CAS  Google Scholar 

  91. Vogel C, Cobleigh M, Tripathy D, et al. Efficacy and safety of trastuzumab as a single agent in first-line treatment of HER2-overexpressing metastatic breast cancer. J Clin Oncol 2002; 20(3): 719–26

    Article  PubMed  CAS  Google Scholar 

  92. Slamon J, Leyland-Jones B, Shak S, et al. Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpreses HER2. N Engl J Med 2001; 344: 783–92

    Article  PubMed  CAS  Google Scholar 

  93. Seidman A, Hudis C, Pierri M, et al. Cardiac dysfunction in the trastuzumab clinical trials experience. J Clin Oncol 2002; 20(5): 1215–21

    Article  PubMed  CAS  Google Scholar 

  94. Ciardiello F, Caputo R, Bianco R, et al. Antitumor effect and potentiation of cytotoxic drugs activity in human cancer cells by ZD1839 (Iressa), an epidermal growth factor receptor-selective tyrosine kinase inhibitor. Clin Cancer Res 2000; 6: 2053–63

    PubMed  CAS  Google Scholar 

  95. Sirotnak F, Zakowski M, Miller V, et al. Efficacy of cytotoxic agents against human tumor xenografts is markedly enhanced by co-administration of ZD1839 (Iressa), an inhibtor of EGFR tyrosine kinase. Clin Cancer Res 2000; 6: 4885–92

    PubMed  CAS  Google Scholar 

  96. Jeng M, Yue W, Eischied A, et al. Role of MAP kinase in the enhanced cell proliferation of long-term estrogen deprived human breast cancer cells. Breast Cancer Res Treat 2000; 62: 167–75

    Article  PubMed  CAS  Google Scholar 

  97. McClelland R, Barrow D, Madden T, et al. Enhanced epidermal growth factor receptor signaling in MCF7 breast cancer cells after long-term culture in the presence of the pure antiestrogen LCI 182,780 (Faslodex). Endocrinology 2001; 142(7): 2776–88

    Article  PubMed  CAS  Google Scholar 

  98. Nicholson R, Hutcheson I, Harper M, et al. Modulation of epidermal growth factor receptor in endocrine-resistant, oestrogen receptor-positive breast cancer. Endocr Relat Cancer 2001; 8: 175–82

    Article  PubMed  CAS  Google Scholar 

  99. Gee J, Hutcheson I, Knowlden J, et al. The EGFR-selective tyrosine kinase inhibitor ZD1839 (Iressa) is an effective inhibitor of tarnoxifen-resistant breast cancer growth. Proc Am Soc Clin Oncol 2001; 20: A282

    Google Scholar 

  100. Clark G, Der CJ. Aberrant function of the Ras signal transduction pathway in human breast cancer. Breast Cancer Res Treat 1995; 35: 133–44

    Article  PubMed  CAS  Google Scholar 

  101. Johnston S, Hickish T, Ellis P, et al. Clinical activity with the farnesyl transferase inhibitor R115777 in patients with advanced breast cancer: relationship with tumour phenotype. Breast Cancer Res Treat 2000; 32: A28

    Google Scholar 

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The author has received funding from the Jansen Research Foundation, AstraZenica and Novatis.

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Assersohn, L., Johnston, S.R. Postmenopausal Metastatic Breast Cancer. Am J Cancer 2, 95–109 (2003). https://doi.org/10.2165/00024669-200302020-00003

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