A randomized comparative study of high-dose and low-dose hepatic arterial infusion chemotherapy for intractable, advanced hepatocellular carcinoma
Purpose Hepatic arterial infusion chemotherapy (HAIC) has been reported to be effective in patients with advanced hepatocellular carcinoma (HCC). Methods In this multicenter, prospective, open-labeled, clinical trial, we randomly assigned 68 patients with advanced HCC to receive either low-dose [n =...
Ausführliche Beschreibung
Autor*in: |
Woo, Hyun Young [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2009 |
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Schlagwörter: |
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Anmerkung: |
© Springer-Verlag 2009 |
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Übergeordnetes Werk: |
Enthalten in: Cancer chemotherapy and pharmacology - Berlin : Springer, 1978, 65(2009), 2 vom: 18. Sept. |
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Übergeordnetes Werk: |
volume:65 ; year:2009 ; number:2 ; day:18 ; month:09 |
Links: |
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DOI / URN: |
10.1007/s00280-009-1126-2 |
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Katalog-ID: |
SPR00359422X |
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100 | 1 | |a Woo, Hyun Young |e verfasserin |4 aut | |
245 | 1 | 2 | |a A randomized comparative study of high-dose and low-dose hepatic arterial infusion chemotherapy for intractable, advanced hepatocellular carcinoma |
264 | 1 | |c 2009 | |
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520 | |a Purpose Hepatic arterial infusion chemotherapy (HAIC) has been reported to be effective in patients with advanced hepatocellular carcinoma (HCC). Methods In this multicenter, prospective, open-labeled, clinical trial, we randomly assigned 68 patients with advanced HCC to receive either low-dose [n = 32, 5-fluorouracil (FU), 170 mg/$ m^{2} $ and cisplatin, 7 mg/$ m^{2} $ on days 1–5] or high-dose HAIC (n = 36, 5-FU, 500 mg/$ m^{2} $ on days 1–3 and cisplatin, 60 mg/$ m^{2} $ on day 2) every 4 weeks via an implantable port system. Results A total of 207 cycles of HAIC was given to the 68 patients. Overall, 6 patients (8.8%) achieved a partial response and 21 patients (30.9%) had stable disease. The objective response rate (CR + PR) was significantly improved in the high-dose group compared to the low-dose group (16.7% vs. 0%, P = 0.024). The median time to disease progression and overall survival were slightly prolonged in the high-dose group compared to the low-dose group (median survival, 193 vs. 153 days; P = 0.108; median time to disease progression, 145 vs. 90 days; P = 0.095). Multivariate analysis showed that tumor response to treatment [P = 0.007, RR 2.27 (95% CI, 1.248–4.132)] was the only factor associated with overall survival. All adverse events were tolerable and successfully managed in both treatment groups. Conclusions Both HAIC regimens are safe and effective in patients with advanced HCC. High-dose HAIC achieves a better tumor response compared to low-dose HAIC. | ||
650 | 4 | |a Hepatocellular carcinoma |7 (dpeaa)DE-He213 | |
650 | 4 | |a Hepatic arterial infusion chemotherapy |7 (dpeaa)DE-He213 | |
650 | 4 | |a High dose |7 (dpeaa)DE-He213 | |
650 | 4 | |a Low dose |7 (dpeaa)DE-He213 | |
650 | 4 | |a 5-Fluorouracil |7 (dpeaa)DE-He213 | |
650 | 4 | |a Cisplatin |7 (dpeaa)DE-He213 | |
700 | 1 | |a Bae, Si Hyun |4 aut | |
700 | 1 | |a Park, Jun Yong |4 aut | |
700 | 1 | |a Han, Kwang Hyub |4 aut | |
700 | 1 | |a Chun, Ho Jong |4 aut | |
700 | 1 | |a Choi, Byung Gil |4 aut | |
700 | 1 | |a Im, Hyeon U. |4 aut | |
700 | 1 | |a Choi, Jong Young |4 aut | |
700 | 1 | |a Yoon, Seung Kew |4 aut | |
700 | 1 | |a Cheong, Jae Youn |4 aut | |
700 | 1 | |a Cho, Sung Won |4 aut | |
700 | 1 | |a Jang, Byoung Kuk |4 aut | |
700 | 1 | |a Hwang, Jae Seok |4 aut | |
700 | 1 | |a Kim, Sang Gyune |4 aut | |
700 | 1 | |a Kim, Young Seok |4 aut | |
700 | 1 | |a Seo, Yeon Seok |4 aut | |
700 | 1 | |a Yim, Hyung Joon |4 aut | |
700 | 1 | |a Um, Soon Ho |4 aut | |
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10.1007/s00280-009-1126-2 doi (DE-627)SPR00359422X (SPR)s00280-009-1126-2-e DE-627 ger DE-627 rakwb eng Woo, Hyun Young verfasserin aut A randomized comparative study of high-dose and low-dose hepatic arterial infusion chemotherapy for intractable, advanced hepatocellular carcinoma 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2009 Purpose Hepatic arterial infusion chemotherapy (HAIC) has been reported to be effective in patients with advanced hepatocellular carcinoma (HCC). Methods In this multicenter, prospective, open-labeled, clinical trial, we randomly assigned 68 patients with advanced HCC to receive either low-dose [n = 32, 5-fluorouracil (FU), 170 mg/$ m^{2} $ and cisplatin, 7 mg/$ m^{2} $ on days 1–5] or high-dose HAIC (n = 36, 5-FU, 500 mg/$ m^{2} $ on days 1–3 and cisplatin, 60 mg/$ m^{2} $ on day 2) every 4 weeks via an implantable port system. Results A total of 207 cycles of HAIC was given to the 68 patients. Overall, 6 patients (8.8%) achieved a partial response and 21 patients (30.9%) had stable disease. The objective response rate (CR + PR) was significantly improved in the high-dose group compared to the low-dose group (16.7% vs. 0%, P = 0.024). The median time to disease progression and overall survival were slightly prolonged in the high-dose group compared to the low-dose group (median survival, 193 vs. 153 days; P = 0.108; median time to disease progression, 145 vs. 90 days; P = 0.095). Multivariate analysis showed that tumor response to treatment [P = 0.007, RR 2.27 (95% CI, 1.248–4.132)] was the only factor associated with overall survival. All adverse events were tolerable and successfully managed in both treatment groups. Conclusions Both HAIC regimens are safe and effective in patients with advanced HCC. High-dose HAIC achieves a better tumor response compared to low-dose HAIC. Hepatocellular carcinoma (dpeaa)DE-He213 Hepatic arterial infusion chemotherapy (dpeaa)DE-He213 High dose (dpeaa)DE-He213 Low dose (dpeaa)DE-He213 5-Fluorouracil (dpeaa)DE-He213 Cisplatin (dpeaa)DE-He213 Bae, Si Hyun aut Park, Jun Yong aut Han, Kwang Hyub aut Chun, Ho Jong aut Choi, Byung Gil aut Im, Hyeon U. aut Choi, Jong Young aut Yoon, Seung Kew aut Cheong, Jae Youn aut Cho, Sung Won aut Jang, Byoung Kuk aut Hwang, Jae Seok aut Kim, Sang Gyune aut Kim, Young Seok aut Seo, Yeon Seok aut Yim, Hyung Joon aut Um, Soon Ho aut Enthalten in Cancer chemotherapy and pharmacology Berlin : Springer, 1978 65(2009), 2 vom: 18. Sept. (DE-627)253390435 (DE-600)1458488-8 1432-0843 nnns volume:65 year:2009 number:2 day:18 month:09 https://dx.doi.org/10.1007/s00280-009-1126-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 65 2009 2 18 09 |
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10.1007/s00280-009-1126-2 doi (DE-627)SPR00359422X (SPR)s00280-009-1126-2-e DE-627 ger DE-627 rakwb eng Woo, Hyun Young verfasserin aut A randomized comparative study of high-dose and low-dose hepatic arterial infusion chemotherapy for intractable, advanced hepatocellular carcinoma 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2009 Purpose Hepatic arterial infusion chemotherapy (HAIC) has been reported to be effective in patients with advanced hepatocellular carcinoma (HCC). Methods In this multicenter, prospective, open-labeled, clinical trial, we randomly assigned 68 patients with advanced HCC to receive either low-dose [n = 32, 5-fluorouracil (FU), 170 mg/$ m^{2} $ and cisplatin, 7 mg/$ m^{2} $ on days 1–5] or high-dose HAIC (n = 36, 5-FU, 500 mg/$ m^{2} $ on days 1–3 and cisplatin, 60 mg/$ m^{2} $ on day 2) every 4 weeks via an implantable port system. Results A total of 207 cycles of HAIC was given to the 68 patients. Overall, 6 patients (8.8%) achieved a partial response and 21 patients (30.9%) had stable disease. The objective response rate (CR + PR) was significantly improved in the high-dose group compared to the low-dose group (16.7% vs. 0%, P = 0.024). The median time to disease progression and overall survival were slightly prolonged in the high-dose group compared to the low-dose group (median survival, 193 vs. 153 days; P = 0.108; median time to disease progression, 145 vs. 90 days; P = 0.095). Multivariate analysis showed that tumor response to treatment [P = 0.007, RR 2.27 (95% CI, 1.248–4.132)] was the only factor associated with overall survival. All adverse events were tolerable and successfully managed in both treatment groups. Conclusions Both HAIC regimens are safe and effective in patients with advanced HCC. High-dose HAIC achieves a better tumor response compared to low-dose HAIC. Hepatocellular carcinoma (dpeaa)DE-He213 Hepatic arterial infusion chemotherapy (dpeaa)DE-He213 High dose (dpeaa)DE-He213 Low dose (dpeaa)DE-He213 5-Fluorouracil (dpeaa)DE-He213 Cisplatin (dpeaa)DE-He213 Bae, Si Hyun aut Park, Jun Yong aut Han, Kwang Hyub aut Chun, Ho Jong aut Choi, Byung Gil aut Im, Hyeon U. aut Choi, Jong Young aut Yoon, Seung Kew aut Cheong, Jae Youn aut Cho, Sung Won aut Jang, Byoung Kuk aut Hwang, Jae Seok aut Kim, Sang Gyune aut Kim, Young Seok aut Seo, Yeon Seok aut Yim, Hyung Joon aut Um, Soon Ho aut Enthalten in Cancer chemotherapy and pharmacology Berlin : Springer, 1978 65(2009), 2 vom: 18. Sept. (DE-627)253390435 (DE-600)1458488-8 1432-0843 nnns volume:65 year:2009 number:2 day:18 month:09 https://dx.doi.org/10.1007/s00280-009-1126-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 65 2009 2 18 09 |
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10.1007/s00280-009-1126-2 doi (DE-627)SPR00359422X (SPR)s00280-009-1126-2-e DE-627 ger DE-627 rakwb eng Woo, Hyun Young verfasserin aut A randomized comparative study of high-dose and low-dose hepatic arterial infusion chemotherapy for intractable, advanced hepatocellular carcinoma 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2009 Purpose Hepatic arterial infusion chemotherapy (HAIC) has been reported to be effective in patients with advanced hepatocellular carcinoma (HCC). Methods In this multicenter, prospective, open-labeled, clinical trial, we randomly assigned 68 patients with advanced HCC to receive either low-dose [n = 32, 5-fluorouracil (FU), 170 mg/$ m^{2} $ and cisplatin, 7 mg/$ m^{2} $ on days 1–5] or high-dose HAIC (n = 36, 5-FU, 500 mg/$ m^{2} $ on days 1–3 and cisplatin, 60 mg/$ m^{2} $ on day 2) every 4 weeks via an implantable port system. Results A total of 207 cycles of HAIC was given to the 68 patients. Overall, 6 patients (8.8%) achieved a partial response and 21 patients (30.9%) had stable disease. The objective response rate (CR + PR) was significantly improved in the high-dose group compared to the low-dose group (16.7% vs. 0%, P = 0.024). The median time to disease progression and overall survival were slightly prolonged in the high-dose group compared to the low-dose group (median survival, 193 vs. 153 days; P = 0.108; median time to disease progression, 145 vs. 90 days; P = 0.095). Multivariate analysis showed that tumor response to treatment [P = 0.007, RR 2.27 (95% CI, 1.248–4.132)] was the only factor associated with overall survival. All adverse events were tolerable and successfully managed in both treatment groups. Conclusions Both HAIC regimens are safe and effective in patients with advanced HCC. High-dose HAIC achieves a better tumor response compared to low-dose HAIC. Hepatocellular carcinoma (dpeaa)DE-He213 Hepatic arterial infusion chemotherapy (dpeaa)DE-He213 High dose (dpeaa)DE-He213 Low dose (dpeaa)DE-He213 5-Fluorouracil (dpeaa)DE-He213 Cisplatin (dpeaa)DE-He213 Bae, Si Hyun aut Park, Jun Yong aut Han, Kwang Hyub aut Chun, Ho Jong aut Choi, Byung Gil aut Im, Hyeon U. aut Choi, Jong Young aut Yoon, Seung Kew aut Cheong, Jae Youn aut Cho, Sung Won aut Jang, Byoung Kuk aut Hwang, Jae Seok aut Kim, Sang Gyune aut Kim, Young Seok aut Seo, Yeon Seok aut Yim, Hyung Joon aut Um, Soon Ho aut Enthalten in Cancer chemotherapy and pharmacology Berlin : Springer, 1978 65(2009), 2 vom: 18. Sept. (DE-627)253390435 (DE-600)1458488-8 1432-0843 nnns volume:65 year:2009 number:2 day:18 month:09 https://dx.doi.org/10.1007/s00280-009-1126-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 65 2009 2 18 09 |
allfieldsGer |
10.1007/s00280-009-1126-2 doi (DE-627)SPR00359422X (SPR)s00280-009-1126-2-e DE-627 ger DE-627 rakwb eng Woo, Hyun Young verfasserin aut A randomized comparative study of high-dose and low-dose hepatic arterial infusion chemotherapy for intractable, advanced hepatocellular carcinoma 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2009 Purpose Hepatic arterial infusion chemotherapy (HAIC) has been reported to be effective in patients with advanced hepatocellular carcinoma (HCC). Methods In this multicenter, prospective, open-labeled, clinical trial, we randomly assigned 68 patients with advanced HCC to receive either low-dose [n = 32, 5-fluorouracil (FU), 170 mg/$ m^{2} $ and cisplatin, 7 mg/$ m^{2} $ on days 1–5] or high-dose HAIC (n = 36, 5-FU, 500 mg/$ m^{2} $ on days 1–3 and cisplatin, 60 mg/$ m^{2} $ on day 2) every 4 weeks via an implantable port system. Results A total of 207 cycles of HAIC was given to the 68 patients. Overall, 6 patients (8.8%) achieved a partial response and 21 patients (30.9%) had stable disease. The objective response rate (CR + PR) was significantly improved in the high-dose group compared to the low-dose group (16.7% vs. 0%, P = 0.024). The median time to disease progression and overall survival were slightly prolonged in the high-dose group compared to the low-dose group (median survival, 193 vs. 153 days; P = 0.108; median time to disease progression, 145 vs. 90 days; P = 0.095). Multivariate analysis showed that tumor response to treatment [P = 0.007, RR 2.27 (95% CI, 1.248–4.132)] was the only factor associated with overall survival. All adverse events were tolerable and successfully managed in both treatment groups. Conclusions Both HAIC regimens are safe and effective in patients with advanced HCC. High-dose HAIC achieves a better tumor response compared to low-dose HAIC. Hepatocellular carcinoma (dpeaa)DE-He213 Hepatic arterial infusion chemotherapy (dpeaa)DE-He213 High dose (dpeaa)DE-He213 Low dose (dpeaa)DE-He213 5-Fluorouracil (dpeaa)DE-He213 Cisplatin (dpeaa)DE-He213 Bae, Si Hyun aut Park, Jun Yong aut Han, Kwang Hyub aut Chun, Ho Jong aut Choi, Byung Gil aut Im, Hyeon U. aut Choi, Jong Young aut Yoon, Seung Kew aut Cheong, Jae Youn aut Cho, Sung Won aut Jang, Byoung Kuk aut Hwang, Jae Seok aut Kim, Sang Gyune aut Kim, Young Seok aut Seo, Yeon Seok aut Yim, Hyung Joon aut Um, Soon Ho aut Enthalten in Cancer chemotherapy and pharmacology Berlin : Springer, 1978 65(2009), 2 vom: 18. Sept. (DE-627)253390435 (DE-600)1458488-8 1432-0843 nnns volume:65 year:2009 number:2 day:18 month:09 https://dx.doi.org/10.1007/s00280-009-1126-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 65 2009 2 18 09 |
allfieldsSound |
10.1007/s00280-009-1126-2 doi (DE-627)SPR00359422X (SPR)s00280-009-1126-2-e DE-627 ger DE-627 rakwb eng Woo, Hyun Young verfasserin aut A randomized comparative study of high-dose and low-dose hepatic arterial infusion chemotherapy for intractable, advanced hepatocellular carcinoma 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2009 Purpose Hepatic arterial infusion chemotherapy (HAIC) has been reported to be effective in patients with advanced hepatocellular carcinoma (HCC). Methods In this multicenter, prospective, open-labeled, clinical trial, we randomly assigned 68 patients with advanced HCC to receive either low-dose [n = 32, 5-fluorouracil (FU), 170 mg/$ m^{2} $ and cisplatin, 7 mg/$ m^{2} $ on days 1–5] or high-dose HAIC (n = 36, 5-FU, 500 mg/$ m^{2} $ on days 1–3 and cisplatin, 60 mg/$ m^{2} $ on day 2) every 4 weeks via an implantable port system. Results A total of 207 cycles of HAIC was given to the 68 patients. Overall, 6 patients (8.8%) achieved a partial response and 21 patients (30.9%) had stable disease. The objective response rate (CR + PR) was significantly improved in the high-dose group compared to the low-dose group (16.7% vs. 0%, P = 0.024). The median time to disease progression and overall survival were slightly prolonged in the high-dose group compared to the low-dose group (median survival, 193 vs. 153 days; P = 0.108; median time to disease progression, 145 vs. 90 days; P = 0.095). Multivariate analysis showed that tumor response to treatment [P = 0.007, RR 2.27 (95% CI, 1.248–4.132)] was the only factor associated with overall survival. All adverse events were tolerable and successfully managed in both treatment groups. Conclusions Both HAIC regimens are safe and effective in patients with advanced HCC. High-dose HAIC achieves a better tumor response compared to low-dose HAIC. Hepatocellular carcinoma (dpeaa)DE-He213 Hepatic arterial infusion chemotherapy (dpeaa)DE-He213 High dose (dpeaa)DE-He213 Low dose (dpeaa)DE-He213 5-Fluorouracil (dpeaa)DE-He213 Cisplatin (dpeaa)DE-He213 Bae, Si Hyun aut Park, Jun Yong aut Han, Kwang Hyub aut Chun, Ho Jong aut Choi, Byung Gil aut Im, Hyeon U. aut Choi, Jong Young aut Yoon, Seung Kew aut Cheong, Jae Youn aut Cho, Sung Won aut Jang, Byoung Kuk aut Hwang, Jae Seok aut Kim, Sang Gyune aut Kim, Young Seok aut Seo, Yeon Seok aut Yim, Hyung Joon aut Um, Soon Ho aut Enthalten in Cancer chemotherapy and pharmacology Berlin : Springer, 1978 65(2009), 2 vom: 18. Sept. (DE-627)253390435 (DE-600)1458488-8 1432-0843 nnns volume:65 year:2009 number:2 day:18 month:09 https://dx.doi.org/10.1007/s00280-009-1126-2 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_711 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 65 2009 2 18 09 |
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English |
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Enthalten in Cancer chemotherapy and pharmacology 65(2009), 2 vom: 18. Sept. volume:65 year:2009 number:2 day:18 month:09 |
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Enthalten in Cancer chemotherapy and pharmacology 65(2009), 2 vom: 18. Sept. volume:65 year:2009 number:2 day:18 month:09 |
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Article |
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Hepatocellular carcinoma Hepatic arterial infusion chemotherapy High dose Low dose 5-Fluorouracil Cisplatin |
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Cancer chemotherapy and pharmacology |
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Woo, Hyun Young @@aut@@ Bae, Si Hyun @@aut@@ Park, Jun Yong @@aut@@ Han, Kwang Hyub @@aut@@ Chun, Ho Jong @@aut@@ Choi, Byung Gil @@aut@@ Im, Hyeon U. @@aut@@ Choi, Jong Young @@aut@@ Yoon, Seung Kew @@aut@@ Cheong, Jae Youn @@aut@@ Cho, Sung Won @@aut@@ Jang, Byoung Kuk @@aut@@ Hwang, Jae Seok @@aut@@ Kim, Sang Gyune @@aut@@ Kim, Young Seok @@aut@@ Seo, Yeon Seok @@aut@@ Yim, Hyung Joon @@aut@@ Um, Soon Ho @@aut@@ |
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2009-09-18T00:00:00Z |
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Methods In this multicenter, prospective, open-labeled, clinical trial, we randomly assigned 68 patients with advanced HCC to receive either low-dose [n = 32, 5-fluorouracil (FU), 170 mg/$ m^{2} $ and cisplatin, 7 mg/$ m^{2} $ on days 1–5] or high-dose HAIC (n = 36, 5-FU, 500 mg/$ m^{2} $ on days 1–3 and cisplatin, 60 mg/$ m^{2} $ on day 2) every 4 weeks via an implantable port system. Results A total of 207 cycles of HAIC was given to the 68 patients. Overall, 6 patients (8.8%) achieved a partial response and 21 patients (30.9%) had stable disease. The objective response rate (CR + PR) was significantly improved in the high-dose group compared to the low-dose group (16.7% vs. 0%, P = 0.024). The median time to disease progression and overall survival were slightly prolonged in the high-dose group compared to the low-dose group (median survival, 193 vs. 153 days; P = 0.108; median time to disease progression, 145 vs. 90 days; P = 0.095). Multivariate analysis showed that tumor response to treatment [P = 0.007, RR 2.27 (95% CI, 1.248–4.132)] was the only factor associated with overall survival. All adverse events were tolerable and successfully managed in both treatment groups. Conclusions Both HAIC regimens are safe and effective in patients with advanced HCC. 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|
author |
Woo, Hyun Young |
spellingShingle |
Woo, Hyun Young misc Hepatocellular carcinoma misc Hepatic arterial infusion chemotherapy misc High dose misc Low dose misc 5-Fluorouracil misc Cisplatin A randomized comparative study of high-dose and low-dose hepatic arterial infusion chemotherapy for intractable, advanced hepatocellular carcinoma |
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Woo, Hyun Young |
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1432-0843 |
topic_title |
A randomized comparative study of high-dose and low-dose hepatic arterial infusion chemotherapy for intractable, advanced hepatocellular carcinoma Hepatocellular carcinoma (dpeaa)DE-He213 Hepatic arterial infusion chemotherapy (dpeaa)DE-He213 High dose (dpeaa)DE-He213 Low dose (dpeaa)DE-He213 5-Fluorouracil (dpeaa)DE-He213 Cisplatin (dpeaa)DE-He213 |
topic |
misc Hepatocellular carcinoma misc Hepatic arterial infusion chemotherapy misc High dose misc Low dose misc 5-Fluorouracil misc Cisplatin |
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misc Hepatocellular carcinoma misc Hepatic arterial infusion chemotherapy misc High dose misc Low dose misc 5-Fluorouracil misc Cisplatin |
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misc Hepatocellular carcinoma misc Hepatic arterial infusion chemotherapy misc High dose misc Low dose misc 5-Fluorouracil misc Cisplatin |
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Cancer chemotherapy and pharmacology |
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A randomized comparative study of high-dose and low-dose hepatic arterial infusion chemotherapy for intractable, advanced hepatocellular carcinoma |
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A randomized comparative study of high-dose and low-dose hepatic arterial infusion chemotherapy for intractable, advanced hepatocellular carcinoma |
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Woo, Hyun Young |
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Cancer chemotherapy and pharmacology |
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2009 |
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Woo, Hyun Young Bae, Si Hyun Park, Jun Yong Han, Kwang Hyub Chun, Ho Jong Choi, Byung Gil Im, Hyeon U. Choi, Jong Young Yoon, Seung Kew Cheong, Jae Youn Cho, Sung Won Jang, Byoung Kuk Hwang, Jae Seok Kim, Sang Gyune Kim, Young Seok Seo, Yeon Seok Yim, Hyung Joon Um, Soon Ho |
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Elektronische Aufsätze |
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Woo, Hyun Young |
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10.1007/s00280-009-1126-2 |
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randomized comparative study of high-dose and low-dose hepatic arterial infusion chemotherapy for intractable, advanced hepatocellular carcinoma |
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A randomized comparative study of high-dose and low-dose hepatic arterial infusion chemotherapy for intractable, advanced hepatocellular carcinoma |
abstract |
Purpose Hepatic arterial infusion chemotherapy (HAIC) has been reported to be effective in patients with advanced hepatocellular carcinoma (HCC). Methods In this multicenter, prospective, open-labeled, clinical trial, we randomly assigned 68 patients with advanced HCC to receive either low-dose [n = 32, 5-fluorouracil (FU), 170 mg/$ m^{2} $ and cisplatin, 7 mg/$ m^{2} $ on days 1–5] or high-dose HAIC (n = 36, 5-FU, 500 mg/$ m^{2} $ on days 1–3 and cisplatin, 60 mg/$ m^{2} $ on day 2) every 4 weeks via an implantable port system. Results A total of 207 cycles of HAIC was given to the 68 patients. Overall, 6 patients (8.8%) achieved a partial response and 21 patients (30.9%) had stable disease. The objective response rate (CR + PR) was significantly improved in the high-dose group compared to the low-dose group (16.7% vs. 0%, P = 0.024). The median time to disease progression and overall survival were slightly prolonged in the high-dose group compared to the low-dose group (median survival, 193 vs. 153 days; P = 0.108; median time to disease progression, 145 vs. 90 days; P = 0.095). Multivariate analysis showed that tumor response to treatment [P = 0.007, RR 2.27 (95% CI, 1.248–4.132)] was the only factor associated with overall survival. All adverse events were tolerable and successfully managed in both treatment groups. Conclusions Both HAIC regimens are safe and effective in patients with advanced HCC. High-dose HAIC achieves a better tumor response compared to low-dose HAIC. © Springer-Verlag 2009 |
abstractGer |
Purpose Hepatic arterial infusion chemotherapy (HAIC) has been reported to be effective in patients with advanced hepatocellular carcinoma (HCC). Methods In this multicenter, prospective, open-labeled, clinical trial, we randomly assigned 68 patients with advanced HCC to receive either low-dose [n = 32, 5-fluorouracil (FU), 170 mg/$ m^{2} $ and cisplatin, 7 mg/$ m^{2} $ on days 1–5] or high-dose HAIC (n = 36, 5-FU, 500 mg/$ m^{2} $ on days 1–3 and cisplatin, 60 mg/$ m^{2} $ on day 2) every 4 weeks via an implantable port system. Results A total of 207 cycles of HAIC was given to the 68 patients. Overall, 6 patients (8.8%) achieved a partial response and 21 patients (30.9%) had stable disease. The objective response rate (CR + PR) was significantly improved in the high-dose group compared to the low-dose group (16.7% vs. 0%, P = 0.024). The median time to disease progression and overall survival were slightly prolonged in the high-dose group compared to the low-dose group (median survival, 193 vs. 153 days; P = 0.108; median time to disease progression, 145 vs. 90 days; P = 0.095). Multivariate analysis showed that tumor response to treatment [P = 0.007, RR 2.27 (95% CI, 1.248–4.132)] was the only factor associated with overall survival. All adverse events were tolerable and successfully managed in both treatment groups. Conclusions Both HAIC regimens are safe and effective in patients with advanced HCC. High-dose HAIC achieves a better tumor response compared to low-dose HAIC. © Springer-Verlag 2009 |
abstract_unstemmed |
Purpose Hepatic arterial infusion chemotherapy (HAIC) has been reported to be effective in patients with advanced hepatocellular carcinoma (HCC). Methods In this multicenter, prospective, open-labeled, clinical trial, we randomly assigned 68 patients with advanced HCC to receive either low-dose [n = 32, 5-fluorouracil (FU), 170 mg/$ m^{2} $ and cisplatin, 7 mg/$ m^{2} $ on days 1–5] or high-dose HAIC (n = 36, 5-FU, 500 mg/$ m^{2} $ on days 1–3 and cisplatin, 60 mg/$ m^{2} $ on day 2) every 4 weeks via an implantable port system. Results A total of 207 cycles of HAIC was given to the 68 patients. Overall, 6 patients (8.8%) achieved a partial response and 21 patients (30.9%) had stable disease. The objective response rate (CR + PR) was significantly improved in the high-dose group compared to the low-dose group (16.7% vs. 0%, P = 0.024). The median time to disease progression and overall survival were slightly prolonged in the high-dose group compared to the low-dose group (median survival, 193 vs. 153 days; P = 0.108; median time to disease progression, 145 vs. 90 days; P = 0.095). Multivariate analysis showed that tumor response to treatment [P = 0.007, RR 2.27 (95% CI, 1.248–4.132)] was the only factor associated with overall survival. All adverse events were tolerable and successfully managed in both treatment groups. Conclusions Both HAIC regimens are safe and effective in patients with advanced HCC. High-dose HAIC achieves a better tumor response compared to low-dose HAIC. © Springer-Verlag 2009 |
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A randomized comparative study of high-dose and low-dose hepatic arterial infusion chemotherapy for intractable, advanced hepatocellular carcinoma |
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Bae, Si Hyun Park, Jun Yong Han, Kwang Hyub Chun, Ho Jong Choi, Byung Gil Im, Hyeon U. Choi, Jong Young Yoon, Seung Kew Cheong, Jae Youn Cho, Sung Won Jang, Byoung Kuk Hwang, Jae Seok Kim, Sang Gyune Kim, Young Seok Seo, Yeon Seok Yim, Hyung Joon Um, Soon Ho |
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score |
7.402936 |