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Combination Chemotherapy in the Treatment of Advanced Hodgkin's Disease
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1970
Year
PharmacotherapyMetronomic ChemotherapyImmunotherapyCancer ChemotherapyHematological MalignancyOncologyHematologyRadiation OncologyChemotherapyCancer ResearchHealth SciencesCombination ChemotherapyBone Marrow SuppressionResponse RateForty-three PatientsCancer TreatmentPharmacologyMalignant Blood DisorderMedicine
Patients received a six‑month cyclic combination of vincristine sulfate, nitrogen mustard (or cyclophosphamide), procarbazine hydrochloride, and prednisone. The regimen produced an 81 % complete remission rate, with durable responses (median 29–42 months), a median survival exceeding 42 months, 77 % of complete responders alive at 4 years, 47 % disease‑free, and a 63 % overall 4‑year survival, while bone‑marrow suppression was the main but generally tolerable toxicity.
Forty-three patients with advanced, primarily untreated Hodgkin's disease were treated with a combination of vincristine sulfate, nitrogen mustard (or cyclophosphamide), procarbazine hydrochloride, and prednisone, given in cyclical fashion for 6 months. The limiting toxicity was primarily bone marrow suppression and, although occasionally severe, was generally tolerable. Other toxicity such as alopecia and neurotoxicity were troublesome but reversible. The response rate was superior to that previously reported with the use of single drugs with 35 of 43, or 81% of the patients achieving a complete remission, defined as the complete disappearance of all tumor and return to normal performance status. The duration of these responses after all therapy was discontinued was gratifyingly long, with a median of not less than 29 and not more than 42 months. Seventeen of 35 patients continue free of their disease, and 28 of these 35 are still alive. The median survival of the responding group is greater than 42 months, and life table analysis of the results indicates that of those complete responders at risk for 4 years, 77% remain alive and 47% are continuously free of their disease. The surviving fraction of the entire group at risk 4 years is 63%. It appears that combinations of effective drugs that act by different mechanisms and manifest different toxicities can be used effectively to increase the response rate and probably the survival of patients with sensitive tumors such as Hodgkin's disease.
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