Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.

±Þ¼º °ñ¼ö¼º ¹éÇ÷º´¿¡¼­ Ara-C, Daunorubicin È­Çпä¹ýÀÇ Ä¡·á È¿°ú Effect of Cytosine Arabinoside and Daunorubicin(AD) Combination Chemotherapy in Acute Myelogenous Leukemia

´ëÇѾÏÇÐȸÁö 1997³â 29±Ç 1È£ p.160 ~ 170
¼Ò¼Ó »ó¼¼Á¤º¸
°­¿µ¼÷ Á¤Çö½Ä/±èż®/À±Çü¼±/±èµæÁ¶/À±Á¤È£/À̼º±¤/ÁöÇö±Ô/³²±ÍÇö

Abstract

°á·Ð
ÀúÀÚµéÀº 1989³â 8¿ùºÎÅÍ 1995³â 11¿ù±îÁö Áß¾Ó ±æº´¿ø ³»°ú¿¡¼­ ±Þ¼º °ñ¼ö¼º ¹éÇ÷º´À¸·Î
Áø´Ü ¹Þ°í Ä¡·á°¡ °¡´ÉÇÏ¿´´ø 34¸í¿¡ ´ëÇÏ¿© ara-C¿Í daunorubicinÀ» »ç¿ëÇÑ °üÇØ ¿ä¹ýÀ»
½Ç½ÃÇÏ¿© ´ÙÀ½°ú °°Àº °á°ú¸¦ ¾ò¾ú´Ù.
1) 34¸í Áß 23¸í¿¡¼­ ¿ÏÀü °üÇØ¿¡ µµ´ÞÇÏ¿© 68%ÀÇ ¿ÏÀü °üÇØÀ²À» º¸¿´À¸¸ç, ¿ÏÀü°üÇØÁö¼Ó
±â°£Àº 4 ¡­312+ Áַμ­ Áß¾ÓÄ¡´Â 50ÁÖ¿´´Ù.
2) ÀüüȯÀÚÀÇ »ýÁ¸±â°£ Áß¾ÓÄ¡´Â 62+ÁÖ¿´À¸¸ç, ¿ÏÀü°üÇØ¿¡ µµ´ÞÇÑ È¯ÀÚ Áß
36%¿¡¼­ 5³â ÀÌ»óÀÇ »ýÁ¸À²À» º¸¿´´Ù.
3) ÃÑ 4¿¹¿¡¼­ °ñ¼ö ¿Ü Á¶Á÷À» ħ½ÀÇÑ ¹éÇ÷º´ÀÌ Áø´ÜµÇ¾ú´Âµ¥, M4,
M5a ÀÌ¿Ü¿¡ M2, M3¿¡¼­µµ °¢°¢ 1¿¹¾¿ Áø´ÜµÇ¾ú
´Ù.
4) ³ªÀÌ, Ä¡·á Àü ¹éÇ÷±¸¼ö, blastÀÇ ¹éºÐÀ² µîÀº ¿¹ÈÄ¿¡ ¿µÇâÀ» ¹ÌÄ¡Áö ¾Ê¾Ò´Ù.
#ÃÊ·Ï#
Purpose : Important advances in the treatment of acute myelogenous leukemia have
been made with the introduction of cytosine arabinoside(ara-C) and anthracyclines
(daunorubicin) over the past 20 years. Currently, 60 to 80% of patients with acute
myelogenous leukemia achieve complete remission with induction chemotherapy
consisting of aria-C and daunorubicin(adriamycin) AD('7+3'). The one-fourth of
complete responders will have extended long-term survival and may be cured. Therefore
wetreated patients with acute myelogenous leukemia admitted to our hospital with
AD('7+3') regimen.
Methods : Induction therapy; Thirty four Patients with Previously untreated acute
myelogenous leukemia received AD('7+3') regimen(ara-C, 200 mg/m2/d by
continuous infusion for seven days, and daunorubicin, 45mg/m2/d for 3
days). The second course of therapy was AD('5+2'), if the Patients failed to enter
remission. Consolidation therapy; three cycles of consolidation chemotherapy were
administered with at least 4 week interval following remission. Course 1; ara-C at 100
mg/m2 by subcutaneous injection every 12 hour for seven days,
6-thioguanine at every 12 hour 100 mg/m2 orally every 12 hour for 7
days). Course 2; ara-C(same as course 1) at 100 mg/m2 by subcutaneous
injection every 12 hour for seven days, vincristine at 1.5 mg/m2
(maximum 2 mg) by bolus injection for 1 day, prednisolone at 40
mg/m2(maximum 60 mg) orally for 7 days. Course 3; ara-C(same as
course 1) daunorubicin at 45 mg/m2 by 1 hour infusion for 3 days.
Results : Sixty-eight percent of the 34 patients entered complete remission. The
remission duration for all patients in complete remission ranged from 4 weeks to
3122+ weeks, with the median of 50 weeks. The median duration of
survival in complete responder group was 62 weeks. Twenty-Six percent of patients
with complete remission are alive at 5 years. Cases with extramedullary leukemic
involvement were found in four patients; M2 with orbital mass, M3 and M4 with CNS
leukemia, M5a with subcutaneous nodules. Among the potential prognostic variables
including age, initial WBC count, percent of blast in peripheral blood, none was
statistically related to prognosis.
Conclusion : Combination chemotherapy with cytosine arabinoside and daunorubicin is
a effective regimen for acute myelogenous leukemia as much as other regimen. Further
clinical trials for effective treatment regimen and method are necessary to raise the
complete remission rate.

Å°¿öµå

Chemotherapy; Aute myelogenous leukemia; AD regimen;

¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸

 

µîÀçÀú³Î Á¤º¸

KoreaMed
KAMS