TY - JOUR
T1 - Plasma cell leukemia
T2 - An evaluation of response to therapy
AU - Noel, Pierre
AU - Kyle, Robert A.
N1 - Funding Information:
From the Division of Hematology and Internal Medicine, Mayo Clinic and Mayo Foundation, Rochester, Minnesota. This work was supported in part by Research Grant CA-16835 from the National Institutes of Health, Public Health Service, and the Mayo Comprehensive Cancer Center, Grant CA-15083. Dr. Noel is a Mayo Foundation Scholar. Requests for reprints should be addressed to Dr. Robert A. Kyle, Mayo Clinic, 200 First Street Southwest, Rochester, Minnesota 55905. Manuscript submitted March 25, 1987, and accepted July 20, 1987.
PY - 1987/12
Y1 - 1987/12
N2 - Forty-three patients with plasma cell leukemia were seen at the Mayo Clinic. Twenty-five (58 percent) had primary plasma cell leukemia (diagnosis first made in the leukemic phase) and 18 (42 percent) had secondary plasma cell leukemia (leukemic transformation of a previously diagnosed multiple myeloma). Patients with secondary plasma cell leukemia were older, had a greater incidence of lytic bone lesions, had a lower platelet count, and had a larger M-protein in the serum than did patients with primary plasma cell leukemia. The median survival was 6.8 months for patients with primary plasma cell leukemia and 1.3 months for patients with secondary plasma cell leukemia. In patients with primary plasma cell leukemia, multiple alkylating agents produced a higher response rate than did melphalan, but the median time from treatment to progression or death was not significantly improved with such therapy. Review of the literature also suggests that the response rate is higher with combination chemotherapy than with single alkylating agents. Patients with secondary plasma cell leukemia usually show resistance to any type of chemotherapy and have a short survival.
AB - Forty-three patients with plasma cell leukemia were seen at the Mayo Clinic. Twenty-five (58 percent) had primary plasma cell leukemia (diagnosis first made in the leukemic phase) and 18 (42 percent) had secondary plasma cell leukemia (leukemic transformation of a previously diagnosed multiple myeloma). Patients with secondary plasma cell leukemia were older, had a greater incidence of lytic bone lesions, had a lower platelet count, and had a larger M-protein in the serum than did patients with primary plasma cell leukemia. The median survival was 6.8 months for patients with primary plasma cell leukemia and 1.3 months for patients with secondary plasma cell leukemia. In patients with primary plasma cell leukemia, multiple alkylating agents produced a higher response rate than did melphalan, but the median time from treatment to progression or death was not significantly improved with such therapy. Review of the literature also suggests that the response rate is higher with combination chemotherapy than with single alkylating agents. Patients with secondary plasma cell leukemia usually show resistance to any type of chemotherapy and have a short survival.
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U2 - 10.1016/0002-9343(87)90942-9
DO - 10.1016/0002-9343(87)90942-9
M3 - Article
C2 - 3503574
AN - SCOPUS:0023634218
SN - 0002-9343
VL - 83
SP - 1062
EP - 1068
JO - American Journal of Medicine
JF - American Journal of Medicine
IS - 6
ER -