[Combination chemotherapy with bleomycin, vincristine and methotrexate for stage I non-seminomatous germ cell testicular tumors]. 1983

I Fukui, and M Yokokawa, and M Wakui, and M Washizuka, and M Katoh, and K Igarashi, and S Takeuchi, and S Gotoh, and H Afuso, and Y Tachibana

Ten patients with Stage I non-seminomatous germ cell testicular tumors underwent orchiectomy and combination chemotherapy with bleomycin, vincristine and methotrexate with CF rescue (BOM) as an induction therapy followed by cyclophosphamide, vincristine and methotrexate as a maintenance therapy (COM). The results were as follows: BOM seemed to be effective as a further treatment for Stage I non-seminomatous germ cell testicular tumor patients. All 10 patients are alive and disease-free for a period from 1 year and 6 months to 5 years and 3 months (mean: 3 years and 9 months). The chemotherapy should be continued at least for a year, since relapse occurred in 2 of 4 patients who received only induction therapy. However, they completely responded to other chemotherapy regimens (BVP and BOAM ). BOM and COM therapy were scarcely toxic and no serious side effects were recognized. From the above results, it was considered that combination chemotherapy (BOM and COM) can be an alternative treatment to the conventional retroperitoneal node dissection and radiation therapy for Stage I non-seminomatous germ cell tumors.

UI MeSH Term Description Entries
D008297 Male Males
D008727 Methotrexate An antineoplastic antimetabolite with immunosuppressant properties. It is an inhibitor of TETRAHYDROFOLATE DEHYDROGENASE and prevents the formation of tetrahydrofolate, necessary for synthesis of thymidylate, an essential component of DNA. Amethopterin,Methotrexate Hydrate,Methotrexate Sodium,Methotrexate, (D)-Isomer,Methotrexate, (DL)-Isomer,Methotrexate, Dicesium Salt,Methotrexate, Disodium Salt,Methotrexate, Sodium Salt,Mexate,Dicesium Salt Methotrexate,Hydrate, Methotrexate,Sodium, Methotrexate
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D001761 Bleomycin A complex of related glycopeptide antibiotics from Streptomyces verticillus consisting of bleomycin A2 and B2. It inhibits DNA metabolism and is used as an antineoplastic, especially for solid tumors. BLEO-cell,Blanoxan,Blenoxane,Bleolem,Bleomicina,Bleomycin A(2),Bleomycin A2,Bleomycin B(2),Bleomycin B2,Bleomycin Sulfate,Bleomycins,Bleomycinum Mack,Bléomycine Bellon,BLEO cell,BLEOcell,Bellon, Bléomycine,Mack, Bleomycinum,Sulfate, Bleomycin
D003520 Cyclophosphamide Precursor of an alkylating nitrogen mustard antineoplastic and immunosuppressive agent that must be activated in the LIVER to form the active aldophosphamide. It has been used in the treatment of LYMPHOMA and LEUKEMIA. Its side effect, ALOPECIA, has been used for defleecing sheep. Cyclophosphamide may also cause sterility, birth defects, mutations, and cancer. (+,-)-2-(bis(2-Chloroethyl)amino)tetrahydro-2H-1,3,2-oxazaphosphorine 2-Oxide Monohydrate,B-518,Cyclophosphamide Anhydrous,Cyclophosphamide Monohydrate,Cyclophosphamide, (R)-Isomer,Cyclophosphamide, (S)-Isomer,Cyclophosphane,Cytophosphan,Cytophosphane,Cytoxan,Endoxan,NSC-26271,Neosar,Procytox,Sendoxan,B 518,B518,NSC 26271,NSC26271
D005500 Follow-Up Studies Studies in which individuals or populations are followed to assess the outcome of exposures, procedures, or effects of a characteristic, e.g., occurrence of disease. Followup Studies,Follow Up Studies,Follow-Up Study,Followup Study,Studies, Follow-Up,Studies, Followup,Study, Follow-Up,Study, Followup
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D000971 Antineoplastic Combined Chemotherapy Protocols The use of two or more chemicals simultaneously or sequentially in the drug therapy of neoplasms. The drugs need not be in the same dosage form. Anticancer Drug Combinations,Antineoplastic Agents, Combined,Antineoplastic Chemotherapy Protocols,Antineoplastic Drug Combinations,Cancer Chemotherapy Protocols,Chemotherapy Protocols, Antineoplastic,Drug Combinations, Antineoplastic,Antineoplastic Combined Chemotherapy Regimens,Combined Antineoplastic Agents,Agent, Combined Antineoplastic,Agents, Combined Antineoplastic,Anticancer Drug Combination,Antineoplastic Agent, Combined,Antineoplastic Chemotherapy Protocol,Antineoplastic Drug Combination,Cancer Chemotherapy Protocol,Chemotherapy Protocol, Antineoplastic,Chemotherapy Protocol, Cancer,Chemotherapy Protocols, Cancer,Combinations, Antineoplastic Drug,Combined Antineoplastic Agent,Drug Combination, Anticancer,Drug Combination, Antineoplastic,Drug Combinations, Anticancer,Protocol, Antineoplastic Chemotherapy,Protocol, Cancer Chemotherapy,Protocols, Antineoplastic Chemotherapy,Protocols, Cancer Chemotherapy
D013724 Teratoma A true neoplasm composed of a number of different types of tissue, none of which is native to the area in which it occurs. It is composed of tissues that are derived from three germinal layers, the endoderm, mesoderm, and ectoderm. They are classified histologically as mature (benign) or immature (malignant). (From DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1642) Dysembryoma,Teratoid Tumor,Teratoma, Cystic,Teratoma, Mature,Teratoma, Benign,Teratoma, Immature,Teratoma, Malignant,Benign Teratoma,Benign Teratomas,Dysembryomas,Immature Teratoma,Immature Teratomas,Malignant Teratoma,Malignant Teratomas,Teratoid Tumors,Teratomas,Teratomas, Benign,Teratomas, Immature,Teratomas, Malignant,Tumor, Teratoid,Tumors, Teratoid

Related Publications

I Fukui, and M Yokokawa, and M Wakui, and M Washizuka, and M Katoh, and K Igarashi, and S Takeuchi, and S Gotoh, and H Afuso, and Y Tachibana
October 1995, Gan to kagaku ryoho. Cancer & chemotherapy,
I Fukui, and M Yokokawa, and M Wakui, and M Washizuka, and M Katoh, and K Igarashi, and S Takeuchi, and S Gotoh, and H Afuso, and Y Tachibana
January 2021, Indian journal of urology : IJU : journal of the Urological Society of India,
I Fukui, and M Yokokawa, and M Wakui, and M Washizuka, and M Katoh, and K Igarashi, and S Takeuchi, and S Gotoh, and H Afuso, and Y Tachibana
January 1992, Annales d'urologie,
I Fukui, and M Yokokawa, and M Wakui, and M Washizuka, and M Katoh, and K Igarashi, and S Takeuchi, and S Gotoh, and H Afuso, and Y Tachibana
January 2016, Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti,
I Fukui, and M Yokokawa, and M Wakui, and M Washizuka, and M Katoh, and K Igarashi, and S Takeuchi, and S Gotoh, and H Afuso, and Y Tachibana
July 1986, Journal of clinical oncology : official journal of the American Society of Clinical Oncology,
I Fukui, and M Yokokawa, and M Wakui, and M Washizuka, and M Katoh, and K Igarashi, and S Takeuchi, and S Gotoh, and H Afuso, and Y Tachibana
September 1982, Lancet (London, England),
I Fukui, and M Yokokawa, and M Wakui, and M Washizuka, and M Katoh, and K Igarashi, and S Takeuchi, and S Gotoh, and H Afuso, and Y Tachibana
May 2009, Critical reviews in oncology/hematology,
I Fukui, and M Yokokawa, and M Wakui, and M Washizuka, and M Katoh, and K Igarashi, and S Takeuchi, and S Gotoh, and H Afuso, and Y Tachibana
September 1994, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde,
I Fukui, and M Yokokawa, and M Wakui, and M Washizuka, and M Katoh, and K Igarashi, and S Takeuchi, and S Gotoh, and H Afuso, and Y Tachibana
December 1979, The Medical journal of Australia,
I Fukui, and M Yokokawa, and M Wakui, and M Washizuka, and M Katoh, and K Igarashi, and S Takeuchi, and S Gotoh, and H Afuso, and Y Tachibana
April 1981, British journal of urology,
Copied contents to your clipboard!