1.Combination chemotherapy for the treatment of multiple myeloma.
Hyo Jin KIM ; Chang In SEO ; Keun Chil PARK ; Heung Tae KIM ; Dae Seog HEO ; Yung Hue BANG ; Seonyang PARK ; Byoung Kook KIM ; Noe Kyeong KIM
Journal of the Korean Cancer Association 1992;24(4):577-585
No abstract available.
Drug Therapy, Combination*
;
Multiple Myeloma*
5.Strategic consideration on treatment of multiple myeloma.
Hua JIANG ; Qing YI ; Jian HOU
Chinese Medical Journal 2011;124(19):2965-2968
6.Combination chemotherapy with vincristine, melphalan and prednisone for multiple myeloma.
Tae You KIM ; Dae Seog HEO ; Yung Jue BANG ; Seon Yang PARK ; Byoung Kook KIM ; Noe Kyeong KIM ; Hyo Jin KIM
Korean Journal of Medicine 1993;45(1):1-11
No abstract available.
Drug Therapy, Combination*
;
Melphalan*
;
Multiple Myeloma*
;
Prednisone*
;
Vincristine*
7.A Case of Phagocytic Myeloma after Chemotherapy.
Eun Jung LEE ; Jihyang LIM ; Hae Kyung LEE ; Myungshin KIM ; Yonggoo KIM ; Kyungja HAN ; Chang Suk KANG ; Gibeom KIM
Korean Journal of Hematology 2002;37(2):161-163
Hemophagocytosis by myeloma cells after chemotherapy is a rare phenomenon. We have experienced a case of phagocytic, IgG, Kappa type plasma cell myeloma in a 41-year-old man after chemotherapy. Phagocytosis of erythrocytes and platelets was found.
Adult
;
Drug Therapy*
;
Erythrocytes
;
Humans
;
Immunoglobulin G
;
Multiple Myeloma
;
Phagocytosis
8.Nonsecretory Multiple Myeloma associated with Immune Thrombocytopenia and Complicated by Malignant Ascites.
Hyun Min PARK ; Inho KIM ; Moon Hee LEE ; Jee Young HAN ; Chul Soo KIM
Korean Journal of Hematology 2002;37(2):153-157
Thrombocytopenia is frequently seen in patients with multiple myeloma when most often the etiology is either chemotherapy induced marrow suppression or bone marrow replacement by myeloma cells. But immune thrombocytopenia has only rarely been documented in patients with multiple myeloma. Also ascites caused by peritoneal infiltration with myeloma cell rarely develops in patients with multiple myeloma. We report a patient with nonsecretory multiple myeloma associated with immune thrombocytopenia and complicated by malignant ascites and periumbilical nodules.
Ascites*
;
Bone Marrow
;
Drug Therapy
;
Humans
;
Multiple Myeloma*
;
Thrombocytopenia*
9.High Dose Chemotherapy with Autologous Stem Cell Transplantation on Multiple Myeloma.
Jae Hoon LEE ; Soo Mee BANG ; Seok LEE ; Hyun Soo KIM ; Jin Seok AHN ; Eun Kyung CHO ; Jung Ae LEE ; Myung Ju AHN ; Deog Yeon JO ; Tae You KIM ; Young Suk PARK ; Sung Soo YOON ; Hong Back LEE ; Cheolwon SUH ; Chu Myoung SEONG ; Soon Nam LEE ; Hwi Joong YOON ; Samyong KIM ; Chul Soo KIM ; Seonyang PARK ; Kyung Sam CHO ; Byoung Kook KIM ; Hugh Chul KIM ; Chan H PARK ; Sang Hee KIM
Korean Journal of Hematology 1999;34(2):306-316
No abstract available.
Drug Therapy*
;
Multiple Myeloma*
;
Stem Cell Transplantation*
;
Stem Cells*
10.Evaluation of the Efficacy and Safety of Chemotherapy in Elderly Patients with Multiple Myeloma under Different Frailty Scores.
Ru XUE ; Lu CHENG ; Li-Min SONG ; Yan-Ping MA
Journal of Experimental Hematology 2022;30(1):170-174
OBJECTIVE:
To compare the efficacy and safety of different chemotherapy regimens in elderly multiple myeloma (MM) patients with different Frailty scores.
METHODS:
The clinical data of elderly patients with MM were retrospectively analyzed, including age, treatment regimen, efficacy, adverse reactions, and the Frailty score included in the activity of daily living score, the instrumental activity of daily living scale and the Charlson comorbidity index. The patients were divided into fit group, mediate fit group and frail group according to the scoring standard. The treatment efficiency and adverse reaction rates of elderly MM with different physical conditions treated by different chemotherapy regimens were analyzed.
RESULTS:
Among the 70 patients, the effective rates of the patients in fit group, the mediate fit group, and the frail group were 79.5%, 81%, and 40%, and the effective rates of the fit patients in double and triple groups were 54.5% and 89.3%, 70% and 90.9% for mediate fit patients, 42.9% and 33.3% for frail patients, the triple regimen in fit patients showed obvious advantages, and the difference showed statistically significant (P<0.05), while the efficacy for mediate patients and frail patients showed no significant difference. During the induction of bortezomib, the incidence of adverse reactions for the patients in the triple group (78.6%) was higher than 67.9% in the double group, and the difference showed no statistically significant (P>0.05).There was no significant difference in the 1-year overall survival rate of the patients and with molecular genetic abnormalities among each groups.
CONCLUSION
The therapeutic effect is related to the patient's physical condition. For patients with healthy physique, the triple regimen should be used first. For patients with weak physical constitution, the chemotherapy regimen with low drug toxicity should be selected for safety.
Aged
;
Bortezomib
;
Frailty
;
Humans
;
Multiple Myeloma/drug therapy*
;
Retrospective Studies