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Randomized Open Label Phase III Trial of Irinotecan Plus Capecitabine versus Capecitabine Monotherapy in Patients with Metastatic Breast Cancer Previously Treated with Anthracycline and Taxane: PROCEED Trial (KCSG BR 11-01)

PURPOSE: We investigated whether irinotecan plus capecitabine improved progression-free survival (PFS) compared with capecitabine alone in patients with human epidermal growth factor 2 (HER2) negative and anthracycline and taxane pretreated metastatic breast cancer (MBC). MATERIALS AND METHODS: A to...

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Autores principales: Park, In Hae, Im, Seock-Ah, Jung, Kyung Hae, Sohn, Joo Hyuk, Park, Yeon Hee, Lee, Keun Seok, Sim, Sung Hoon, Park, Kyong-Hwa, Kim, Jee Hyun, Nam, Byung Ho, Kim, Hee-Jun, Kim, Tae-Yong, Lee, Kyung-Hun, Kim, Sung-Bae, Ahn, Jin-Hee, Lee, Suee, Ro, Jungsil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Cancer Association 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333992/
https://www.ncbi.nlm.nih.gov/pubmed/29458237
http://dx.doi.org/10.4143/crt.2017.562
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author Park, In Hae
Im, Seock-Ah
Jung, Kyung Hae
Sohn, Joo Hyuk
Park, Yeon Hee
Lee, Keun Seok
Sim, Sung Hoon
Park, Kyong-Hwa
Kim, Jee Hyun
Nam, Byung Ho
Kim, Hee-Jun
Kim, Tae-Yong
Lee, Kyung-Hun
Kim, Sung-Bae
Ahn, Jin-Hee
Lee, Suee
Ro, Jungsil
author_facet Park, In Hae
Im, Seock-Ah
Jung, Kyung Hae
Sohn, Joo Hyuk
Park, Yeon Hee
Lee, Keun Seok
Sim, Sung Hoon
Park, Kyong-Hwa
Kim, Jee Hyun
Nam, Byung Ho
Kim, Hee-Jun
Kim, Tae-Yong
Lee, Kyung-Hun
Kim, Sung-Bae
Ahn, Jin-Hee
Lee, Suee
Ro, Jungsil
author_sort Park, In Hae
collection PubMed
description PURPOSE: We investigated whether irinotecan plus capecitabine improved progression-free survival (PFS) compared with capecitabine alone in patients with human epidermal growth factor 2 (HER2) negative and anthracycline and taxane pretreated metastatic breast cancer (MBC). MATERIALS AND METHODS: A total of 221 patients were randomly assigned to irinotecan (80 mg/m(2), days 1 and 8) and capecitabine (1,000 mg/m(2) twice a day, days 1-14) or capecitabine alone (1,250 mg/m(2) twice a day, days 1-14) every 3 weeks. The primary endpoint was PFS. RESULTS: There was no significant difference in PFS between the combination and monotherapy arm (median, 6.4 months vs. 4.7 months; hazard ratio [HR], 0.84; 95% confidence interval [CI], 0.63 to 1.11; p=0.84). In patients with triple-negative breast cancer (TNBC, n=90), the combination significantly improved PFS (median, 4.7 months vs. 2.5 months; HR, 0.58; 95% CI, 0.37 to 0.91; p=0.02). Objective response rate was numerically higher in the combination arm, though it failed to reach statistical significance (44.4% vs. 33.3%, p=0.30). Overall survival did not differ between arms (median, 20.4 months vs. 24.0 months; p=0.63). While grade 3 or 4 neutropenia was more common in the combination arm (39.6% vs. 9.0%), hand-foot syndrome was more often observed in capecitabine arm. Quality of life measurements in global health status was similar. However, patients in the combination arm showed significantly worse symptom scales especially in nausea/vomiting and diarrhea. CONCLUSION: Irinotecan plus capecitabine did not prove clinically superior to single-agent capecitabine in anthracycline- and taxane-pretreated HER2 negative MBC patients. Toxicity profiles of the two groups differed but were manageable. The role of added irinotecan in patients with TNBC remains to be elucidated.
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spelling pubmed-63339922019-01-22 Randomized Open Label Phase III Trial of Irinotecan Plus Capecitabine versus Capecitabine Monotherapy in Patients with Metastatic Breast Cancer Previously Treated with Anthracycline and Taxane: PROCEED Trial (KCSG BR 11-01) Park, In Hae Im, Seock-Ah Jung, Kyung Hae Sohn, Joo Hyuk Park, Yeon Hee Lee, Keun Seok Sim, Sung Hoon Park, Kyong-Hwa Kim, Jee Hyun Nam, Byung Ho Kim, Hee-Jun Kim, Tae-Yong Lee, Kyung-Hun Kim, Sung-Bae Ahn, Jin-Hee Lee, Suee Ro, Jungsil Cancer Res Treat Original Article PURPOSE: We investigated whether irinotecan plus capecitabine improved progression-free survival (PFS) compared with capecitabine alone in patients with human epidermal growth factor 2 (HER2) negative and anthracycline and taxane pretreated metastatic breast cancer (MBC). MATERIALS AND METHODS: A total of 221 patients were randomly assigned to irinotecan (80 mg/m(2), days 1 and 8) and capecitabine (1,000 mg/m(2) twice a day, days 1-14) or capecitabine alone (1,250 mg/m(2) twice a day, days 1-14) every 3 weeks. The primary endpoint was PFS. RESULTS: There was no significant difference in PFS between the combination and monotherapy arm (median, 6.4 months vs. 4.7 months; hazard ratio [HR], 0.84; 95% confidence interval [CI], 0.63 to 1.11; p=0.84). In patients with triple-negative breast cancer (TNBC, n=90), the combination significantly improved PFS (median, 4.7 months vs. 2.5 months; HR, 0.58; 95% CI, 0.37 to 0.91; p=0.02). Objective response rate was numerically higher in the combination arm, though it failed to reach statistical significance (44.4% vs. 33.3%, p=0.30). Overall survival did not differ between arms (median, 20.4 months vs. 24.0 months; p=0.63). While grade 3 or 4 neutropenia was more common in the combination arm (39.6% vs. 9.0%), hand-foot syndrome was more often observed in capecitabine arm. Quality of life measurements in global health status was similar. However, patients in the combination arm showed significantly worse symptom scales especially in nausea/vomiting and diarrhea. CONCLUSION: Irinotecan plus capecitabine did not prove clinically superior to single-agent capecitabine in anthracycline- and taxane-pretreated HER2 negative MBC patients. Toxicity profiles of the two groups differed but were manageable. The role of added irinotecan in patients with TNBC remains to be elucidated. Korean Cancer Association 2019-01 2018-02-14 /pmc/articles/PMC6333992/ /pubmed/29458237 http://dx.doi.org/10.4143/crt.2017.562 Text en Copyright © 2019 by the Korean Cancer Association This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Park, In Hae
Im, Seock-Ah
Jung, Kyung Hae
Sohn, Joo Hyuk
Park, Yeon Hee
Lee, Keun Seok
Sim, Sung Hoon
Park, Kyong-Hwa
Kim, Jee Hyun
Nam, Byung Ho
Kim, Hee-Jun
Kim, Tae-Yong
Lee, Kyung-Hun
Kim, Sung-Bae
Ahn, Jin-Hee
Lee, Suee
Ro, Jungsil
Randomized Open Label Phase III Trial of Irinotecan Plus Capecitabine versus Capecitabine Monotherapy in Patients with Metastatic Breast Cancer Previously Treated with Anthracycline and Taxane: PROCEED Trial (KCSG BR 11-01)
title Randomized Open Label Phase III Trial of Irinotecan Plus Capecitabine versus Capecitabine Monotherapy in Patients with Metastatic Breast Cancer Previously Treated with Anthracycline and Taxane: PROCEED Trial (KCSG BR 11-01)
title_full Randomized Open Label Phase III Trial of Irinotecan Plus Capecitabine versus Capecitabine Monotherapy in Patients with Metastatic Breast Cancer Previously Treated with Anthracycline and Taxane: PROCEED Trial (KCSG BR 11-01)
title_fullStr Randomized Open Label Phase III Trial of Irinotecan Plus Capecitabine versus Capecitabine Monotherapy in Patients with Metastatic Breast Cancer Previously Treated with Anthracycline and Taxane: PROCEED Trial (KCSG BR 11-01)
title_full_unstemmed Randomized Open Label Phase III Trial of Irinotecan Plus Capecitabine versus Capecitabine Monotherapy in Patients with Metastatic Breast Cancer Previously Treated with Anthracycline and Taxane: PROCEED Trial (KCSG BR 11-01)
title_short Randomized Open Label Phase III Trial of Irinotecan Plus Capecitabine versus Capecitabine Monotherapy in Patients with Metastatic Breast Cancer Previously Treated with Anthracycline and Taxane: PROCEED Trial (KCSG BR 11-01)
title_sort randomized open label phase iii trial of irinotecan plus capecitabine versus capecitabine monotherapy in patients with metastatic breast cancer previously treated with anthracycline and taxane: proceed trial (kcsg br 11-01)
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333992/
https://www.ncbi.nlm.nih.gov/pubmed/29458237
http://dx.doi.org/10.4143/crt.2017.562
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