Cyclical combination chemotherapy for advanced breast carcinoma
- PMID: 4818162
- PMCID: PMC1633086
- DOI: 10.1136/bmj.1.5901.218
Cyclical combination chemotherapy for advanced breast carcinoma
Abstract
Twenty-five patients with advanced metastatic breast cancer were treated with the combination of methotrexate 60 mg/M(2) and 5-fluorouracil 700 mg/M(2) intravenously on the first and eighth days, and cyclophosphamide 100 mg/M(2) and prednisone 40 mg/M(2) by mouth daily for the first 14 days of a 28-day cycle. The patients had had no previous chemotherapy or extensive radiotherapy and all but two had not responded to hormonal therapy or endocrine ablation. The major metastatic lesions were: lung (12 patients), liver (four patients), bone (four patients), soft tissue (three patients), nodes (two patients). Seventeen of the 25 patients (68%) responded to treatment with seven complete remissions; these included patients suffering metastatic lesions in the lung, nodes, and soft tissue. The overall median duration of response was nine months (range 6-26 months). Toxicity was primarily haematological, but the group received an average of at least 75% of their calculated dose for each monthly cycle. Haematological toxicity was most pronounced in patients with liver dysfunction and bone marrow involvement. Out of eight nonresponders seven died, with a median survival of six months. Only six of 17 responders died, and the median survival in this group will exceed thirteen months. There was no correlation between the length of the metastasis-free interval after previous treatment and subsequent response to chemotherapy.
Similar articles
-
Combination chemotherapy for advanced breast cancer: response and effect on survival.Ann Intern Med. 1976 Apr;84(4):389-92. doi: 10.7326/0003-4819-84-4-389. Ann Intern Med. 1976. PMID: 1259283
-
Adjuvant chemotherapy with cyclophosphamide, methotrexate, and 5-fluorouracil, vincristine, and prednisone compared with single-agent L-phenylalanine mustard for patients with operable breast carcinoma and positive axillary lymph nodes: 20-year results of a Southwest Oncology Group study.Cancer. 2003 Jan 1;97(1):21-9. doi: 10.1002/cncr.10982. Cancer. 2003. PMID: 12491501 Clinical Trial.
-
[Chemotherapy of metastasizing breast cancers. Indications and results].Dtsch Med Wochenschr. 1975 Jan 10;100(2):35-41. doi: 10.1055/s-0028-1106166. Dtsch Med Wochenschr. 1975. PMID: 1112210 Clinical Trial. German.
-
Management of breast cancer.Clin Pharm. 1982 Nov-Dec;1(6):515-29. Clin Pharm. 1982. PMID: 6192963 Review.
-
Chemotherapy of skeletal metastases.Int J Radiat Oncol Biol Phys. 1976 Nov-Dec;1(11-12):1211-5. doi: 10.1016/0360-3016(76)90097-3. Int J Radiat Oncol Biol Phys. 1976. PMID: 62744 Review. No abstract available.
Cited by
-
β-Elemene Enhances the Chemotherapeutic Effect of 5-Fluorouracil in Triple-Negative Breast Cancer via PI3K/AKT, RAF-MEK-ErK, and NF-κB Signaling Pathways.Onco Targets Ther. 2020 Jun 9;13:5207-5222. doi: 10.2147/OTT.S242820. eCollection 2020. Onco Targets Ther. 2020. PMID: 32606741 Free PMC article.
-
Combination chemotherapy followed by skin grafts in the management of locally advanced breast cancer.Ann Surg. 1978 Nov;188(5):666-8. doi: 10.1097/00000658-197811000-00014. Ann Surg. 1978. PMID: 363074 Free PMC article.
-
Is it time for a new paradigm for systemic cancer treatment? Lessons from a century of cancer chemotherapy.Front Pharmacol. 2013 Jun 25;4:68. doi: 10.3389/fphar.2013.00068. eCollection 2013. Front Pharmacol. 2013. PMID: 23805101 Free PMC article.
-
Hybrid Drugs-A Strategy for Overcoming Anticancer Drug Resistance?Molecules. 2021 Apr 29;26(9):2601. doi: 10.3390/molecules26092601. Molecules. 2021. PMID: 33946916 Free PMC article. Review.
-
Rationale and methods for the use of nude mice to study the biology and therapy of human cancer metastasis.Cancer Metastasis Rev. 1986;5(1):29-49. doi: 10.1007/BF00049529. Cancer Metastasis Rev. 1986. PMID: 2942306 Review.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources