The Threshold Dose of P32 for Leukemic Cells of the Lymphocytic and Granulocytic Series
Open Access
- 1 August 1960
- journal article
- research article
- Published by American Society of Hematology in Blood
- Vol. 16 (2) , 1104-1121
- https://doi.org/10.1182/blood.v16.2.1104.1104
Abstract
Analyses of the threshold dose of P32 to control 201 chronic lymphocytic leukemia patients and 100 chronic granulocytic leukemia patients and of the P32 dose to maintain 133 chronic lymphocytic leukemia patients for a mean period of 50.2 months and 49 chronic granulocytic leukemia patients for a mean period of 33.6 months are analyzed. These threshold doses fit the logarithmic probability distributions given in the tables and figures. See PDF for Figure See PDF for Figure When the dose in mc. to control was plotted against the leukocyte count, a straight line was obtained on log log paper. The equation for this curve for the median dose to control chronic granulocytic leukemia is: log mc. P32 per 12 weeks = 0.33 log L - 0.633, where L is the leukocyte count on the day the first P32 was given. The equation for the log log curve relating median dose to control chronic lymphocytic leukemia to initial counts above 15,000 is: log mc. P32 per 12 weeks = 0.47 log L - 1.420. But the 40 aleukemic or subleukemic cases with leukocyte counts below 15,000 had a median P32 requirement and standard deviation that did not differ significantly from that for the entire group, suggesting that this subleukemic group includes patients resembling the entire spectrum of cases with elevated initial leukocyte counts. See PDF for Figure See PDF for Figure The median dose of P32 per year to maintain chronic granulocytic leukemia cases fits the equation: log P32 per year = 0.546 log L - 1.506, and the corresponding equation for chronic leukemic lymphocytic leukemia is: log mc. P32 per year = 0.45 log L - 1.22. The group of lymphocytic leukemias with initial counts below 15,000 again showed a median and distribution similar to that for the entire leukemic group. The remarkable fact that the dose requirement years later is related to the initial leukocyte count is discussed. Revised recommendations on dosage schedule for titrated, regularly spaced P32 therapy of the chronic leukemias are presented. For each individual patient with chronic leukemia, there is a threshold dose of intravenously administered P32 below which no effect is observed. The dose and interval which will maintain a uniform leukocyte count of about 15,000 may remain unchanged for years or may show abrupt changes at any time to either a lower or higher requirement.Keywords
This publication has 11 references indexed in Scilit:
- Myeloproliferative Diseases: Clinical and Pathologic Study of 69 CasesAmerican Journal of Clinical Pathology, 1959
- SOME ASPECTS OF DRUG RESISTANCE IN NEOPLASMSAnnals of the New York Academy of Sciences, 1958
- A Unifying Concept of the Etiology of the Leukemias, Lymphomas, and Cancers2JNCI Journal of the National Cancer Institute, 1957
- A Histochemical Procedure for Localizing and Evaluating Leukocyte Alkaline Phosphatase Activity in Smears of Blood and MarrowBlood, 1955
- TREATMENT OF CHRONIC LEUKEMIASJAMA, 1952
- The relative rates of formation of new leukocytes in patients with acute and chronic leukemias.Measured by the uptake of radioactive phosphorus in the isolated desoxyribosenucleic acidCancer, 1952
- The biological half-life of radioactive phosphorus in the blood of patients with leukemia.IV. Leukocytes—radioactive phosphorus content and the relation to plasma-P32 levelsCancer, 1950
- The biological half-life of radioactive phosphorus in the blood of patients with leukemia.III. Erythrocytes—with deviations of observations from predicted valuesCancer, 1950
- The biological half-life of radioactive phosphorus in the blood of patients with leukemia.II. Plasma—with deviations of observations from predicted values and an estimate of total-phosphorus turnover rateCancer, 1950
- The biological half-life of radioactive phosphorus in the blood of patients with leukemia.I. Whole blood—with deviations of observations from predicted values and an estimate of total-phosphorus turnover rateCancer, 1950