Àá½Ã¸¸ ±â´Ù·Á ÁÖ¼¼¿ä. ·ÎµùÁßÀÔ´Ï´Ù.

ÁøÇ༺ ´ëÀå¾Ï¿¡ ´ëÇÑ Leucovorin, 5-Fluorouracil ¹× Cisplatin(LV-FP) º¹ÇÕÈ­Çпä¹ýÀÇ Ä¡·áÈ¿°ú Leucovorin, 5-Fluorouracil and Cisplatin(LV-FP) Chemotherapy for Advanced Colorectal Cancer

´ëÇѾÏÇÐȸÁö 1995³â 27±Ç 1È£ p.44 ~ 51
¼Ò¼Ó »ó¼¼Á¤º¸
À¯¿µÁø ÀÓ¿µÇõ/°­À±±¸/±èºÀ¼®/±èÇü°Ç/¼ÕÅ¿ë/ÀÌ»ó±¸/õÀº¹Ì/±èÀ¯Ã¶

Abstract


The biochemical modulation of 5-fluorouracil(5-FU) by leucovorin has been demonstrated to enhance the activity of 5-FU in patients with advanced colorectal cancer and the synergism between 5-FU and cisplatin is well known in advanced
gastrointestinal
tract cancers. We conducted a phase ¥±trial to evaluated the effect of a combination of leucovorin, 5-FU, and cisplatin(LV FP)in patients with advanced colorectal cancer. LV-FP regimen consisted of leucovorin 20mg/m*/day ¥³ in day 1~5, 5-FU
1.000mg/m*/day continuous ¥³. Infusion in day 1~5, and cisplatin 20mg/m*/day¥³in day 1~5. The regimen was repeated every 3 weeks. Among 46 patients with histologically confirmed advanced colorectal adenocarcinoma, 31 patients had measurable
lesion(s)
with median age of 55 years(22~ 70 years). 27 patients had previous history of chemotherapy and 19 were previously untreated.
There was no complete response. 11 patients responded partially to the regimen to make the response rate 35%(11/31). The median time to progression was 16 weeks(2~44 weeks), and the median survival time was 42 weeks(1+~80 weeks). There was no
difference
I response rates between the previously treated and the previously untreated. Hematologic toxicities were mild and non-hematologic toxicities were also tolerable. There was no treatment-related mortality.
These results indicate that the LV-FP regimen is safe and effective in advanced colorectal adenocarcinoma.

Å°¿öµå

¿ø¹® ¹× ¸µÅ©¾Æ¿ô Á¤º¸

 

µîÀçÀú³Î Á¤º¸

KoreaMed
KAMS