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Metronomic oral chemotherapy with cyclophosphamide plus capecitabine combined with trastuzumab (HEX) as first line therapy of HER-2 positive advanced breast cancer: A phase II trial of the Gruppo Oncologico Italia Meridionale (GOIM)
Background. The combination of chemotherapy plus anti HER-2 agents is the mainstay of HER-2 positive advanced breast cancer (ABC) therapy. We conducted a phase II trial testing activity and safety of trastuzumab and metronomic capecitabine/cyclophosphamide (HEX) as first-line therapy in HER-2 positi...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375616/ https://www.ncbi.nlm.nih.gov/pubmed/32540553 http://dx.doi.org/10.1016/j.breast.2020.06.002 |
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author | Orlando, Laura Lorusso, Vito Giotta, Francesco Di Maio, Massimo Schiavone, Paola Fedele, Palma Quaranta, Annamaria Caliolo, Chiara Ciccarese, Mariangela Cinefra, Margherita Romito, Sante Pisconti, Salvatore Prete, Salvatore del Aieta, Michele Rizzi, Daniele Maiello, Evaristo Colucci, Giuseppe Cinieri, Saverio |
author_facet | Orlando, Laura Lorusso, Vito Giotta, Francesco Di Maio, Massimo Schiavone, Paola Fedele, Palma Quaranta, Annamaria Caliolo, Chiara Ciccarese, Mariangela Cinefra, Margherita Romito, Sante Pisconti, Salvatore Prete, Salvatore del Aieta, Michele Rizzi, Daniele Maiello, Evaristo Colucci, Giuseppe Cinieri, Saverio |
author_sort | Orlando, Laura |
collection | PubMed |
description | Background. The combination of chemotherapy plus anti HER-2 agents is the mainstay of HER-2 positive advanced breast cancer (ABC) therapy. We conducted a phase II trial testing activity and safety of trastuzumab and metronomic capecitabine/cyclophosphamide (HEX) as first-line therapy in HER-2 positive ABC.
Methods. Patients at first relapse or with synchronous metastasis were treated with trastuzumab (4 mg/kg, biweekly) plus oral capecitabine (1500 mg/daily) and cyclophosphamide (50 mg/daily). Primary endpoint was objective response rate (ORR), secondary endpoints progression-free survival (PFS), clinical benefit rate (CBR; PR + CR + SD for ≥ 24 weeks) and tolerability. Optimal two-stage design was applied. Results. Sixty patients with measurable ABC, tumors scored as +3 for HER-2 or FISH +, untreated for advanced disease were enrolled. Median age was 62.5 years, visceral metastases were present in most patients (57.9%). Median number of cycles was 16 (range 1–98). ORR was 56.7% (95% CI, 44.1–68.4%), with 5 CR (8.3%) and 29 PR (48.3%). Fifteen patients had SD (25%). The CBR was 78.2%. Nine progressions were observed (15%). Median PFS was 11 months. One year PFS was 47.7%. Median OS was 45.9 months. Worst toxicities were grade 3 hand-foot syndrome in 2 pts (3.3%), grade 3 anaemia in 2 pts (3.3%), grade 2 nausea in 2 pts (3.3%) and grade 3–4 diarrhea in 2 pts (3.3%). Cardiac toxicity grade 1 was reported in 1 pt. Conclusions. Combination of trastuzumab and metronomic oral chemotherapy has clinical activity. The tolerability was excellent and allowed the prolonged delivery of treatment. |
format | Online Article Text |
id | pubmed-7375616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-73756162020-07-29 Metronomic oral chemotherapy with cyclophosphamide plus capecitabine combined with trastuzumab (HEX) as first line therapy of HER-2 positive advanced breast cancer: A phase II trial of the Gruppo Oncologico Italia Meridionale (GOIM) Orlando, Laura Lorusso, Vito Giotta, Francesco Di Maio, Massimo Schiavone, Paola Fedele, Palma Quaranta, Annamaria Caliolo, Chiara Ciccarese, Mariangela Cinefra, Margherita Romito, Sante Pisconti, Salvatore Prete, Salvatore del Aieta, Michele Rizzi, Daniele Maiello, Evaristo Colucci, Giuseppe Cinieri, Saverio Breast Original Article Background. The combination of chemotherapy plus anti HER-2 agents is the mainstay of HER-2 positive advanced breast cancer (ABC) therapy. We conducted a phase II trial testing activity and safety of trastuzumab and metronomic capecitabine/cyclophosphamide (HEX) as first-line therapy in HER-2 positive ABC.
Methods. Patients at first relapse or with synchronous metastasis were treated with trastuzumab (4 mg/kg, biweekly) plus oral capecitabine (1500 mg/daily) and cyclophosphamide (50 mg/daily). Primary endpoint was objective response rate (ORR), secondary endpoints progression-free survival (PFS), clinical benefit rate (CBR; PR + CR + SD for ≥ 24 weeks) and tolerability. Optimal two-stage design was applied. Results. Sixty patients with measurable ABC, tumors scored as +3 for HER-2 or FISH +, untreated for advanced disease were enrolled. Median age was 62.5 years, visceral metastases were present in most patients (57.9%). Median number of cycles was 16 (range 1–98). ORR was 56.7% (95% CI, 44.1–68.4%), with 5 CR (8.3%) and 29 PR (48.3%). Fifteen patients had SD (25%). The CBR was 78.2%. Nine progressions were observed (15%). Median PFS was 11 months. One year PFS was 47.7%. Median OS was 45.9 months. Worst toxicities were grade 3 hand-foot syndrome in 2 pts (3.3%), grade 3 anaemia in 2 pts (3.3%), grade 2 nausea in 2 pts (3.3%) and grade 3–4 diarrhea in 2 pts (3.3%). Cardiac toxicity grade 1 was reported in 1 pt. Conclusions. Combination of trastuzumab and metronomic oral chemotherapy has clinical activity. The tolerability was excellent and allowed the prolonged delivery of treatment. Elsevier 2020-06-05 /pmc/articles/PMC7375616/ /pubmed/32540553 http://dx.doi.org/10.1016/j.breast.2020.06.002 Text en © 2020 The Authors. Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Orlando, Laura Lorusso, Vito Giotta, Francesco Di Maio, Massimo Schiavone, Paola Fedele, Palma Quaranta, Annamaria Caliolo, Chiara Ciccarese, Mariangela Cinefra, Margherita Romito, Sante Pisconti, Salvatore Prete, Salvatore del Aieta, Michele Rizzi, Daniele Maiello, Evaristo Colucci, Giuseppe Cinieri, Saverio Metronomic oral chemotherapy with cyclophosphamide plus capecitabine combined with trastuzumab (HEX) as first line therapy of HER-2 positive advanced breast cancer: A phase II trial of the Gruppo Oncologico Italia Meridionale (GOIM) |
title | Metronomic oral chemotherapy with cyclophosphamide plus capecitabine combined with trastuzumab (HEX) as first line therapy of HER-2 positive advanced breast cancer: A phase II trial of the Gruppo Oncologico Italia Meridionale (GOIM) |
title_full | Metronomic oral chemotherapy with cyclophosphamide plus capecitabine combined with trastuzumab (HEX) as first line therapy of HER-2 positive advanced breast cancer: A phase II trial of the Gruppo Oncologico Italia Meridionale (GOIM) |
title_fullStr | Metronomic oral chemotherapy with cyclophosphamide plus capecitabine combined with trastuzumab (HEX) as first line therapy of HER-2 positive advanced breast cancer: A phase II trial of the Gruppo Oncologico Italia Meridionale (GOIM) |
title_full_unstemmed | Metronomic oral chemotherapy with cyclophosphamide plus capecitabine combined with trastuzumab (HEX) as first line therapy of HER-2 positive advanced breast cancer: A phase II trial of the Gruppo Oncologico Italia Meridionale (GOIM) |
title_short | Metronomic oral chemotherapy with cyclophosphamide plus capecitabine combined with trastuzumab (HEX) as first line therapy of HER-2 positive advanced breast cancer: A phase II trial of the Gruppo Oncologico Italia Meridionale (GOIM) |
title_sort | metronomic oral chemotherapy with cyclophosphamide plus capecitabine combined with trastuzumab (hex) as first line therapy of her-2 positive advanced breast cancer: a phase ii trial of the gruppo oncologico italia meridionale (goim) |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7375616/ https://www.ncbi.nlm.nih.gov/pubmed/32540553 http://dx.doi.org/10.1016/j.breast.2020.06.002 |
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