Low-Dose Oral Cyclophosphamide and Methotrexate Maintenance for Hormone Receptor-Negative Early Breast Cancer: International Breast Cancer Study Group Trial 22-00
Descripción del Articulo
Purpose: To evaluate the benefit of low-dose cyclophosphamide and methotrexate (CM) maintenance, which previously demonstrated antitumor activity and few adverse effects in advanced breast cancer, in early breast cancer. Patients and methods: International Breast Cancer Study Group (IBCSG) Trial 22-...
Autores: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | artículo |
Fecha de Publicación: | 2017 |
Institución: | Instituto Nacional de Enfermedades Neoplásicas |
Repositorio: | INEN-Institucional |
Lenguaje: | inglés |
OAI Identifier: | oai:repositorio.inen.sld.pe:inen/118 |
Enlace del recurso: | https://repositorio.inen.sld.pe/handle/inen/118 |
Nivel de acceso: | acceso abierto |
Materia: | https://purl.org/pe-repo/ocde/ford#3.02.21 |
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Colleoni, MGray, KPGelber,SLáng, IThürlimann, BGianni, LAbdi, EAGomez, HLinderholm, BKPuglis,i FTondini, CKralidis, EEniu, ACagossi, KRauch, DChirgwin, JGelber, RDRegan, MMCoates, ASPrice, KNViale, GGoldhirsch, A2024-07-01T16:28:50Z2024-07-01T16:28:50Z2017Purpose: To evaluate the benefit of low-dose cyclophosphamide and methotrexate (CM) maintenance, which previously demonstrated antitumor activity and few adverse effects in advanced breast cancer, in early breast cancer. Patients and methods: International Breast Cancer Study Group (IBCSG) Trial 22-00, a randomized phase III clinical trial, enrolled 1,086 women (1,081 intent-to-treat) from November 2000 to December 2012. Women with estrogen receptor- and progesterone receptor-negative (< 10% positive cells by immunohistochemistry) early breast cancer any nodal and human epidermal growth factor receptor 2 status, were randomly assigned anytime between primary surgery and 56 days after the first day of last course of adjuvant chemotherapy to CM maintenance (cyclophosphamide 50 mg/day orally continuously and methotrexate 2.5 mg twice/day orally on days 1 and 2 of every week for 1 year) or to no CM. The primary end point was disease-free survival (DFS), which included invasive recurrences, second (breast and nonbreast) malignancies, and deaths. Results: After a median of 6.9 years of follow-up, DFS was not significantly better for patients assigned to CM maintenance compared with patients assigned to no CM, both overall (hazard ratio [HR], 0.84; 95% CI, 0.66 to 1.06;P = .14) and in triple-negative (TN) disease (n = 814; HR, 0.80; 95% CI, 0.60 to 1.06). Patients with TN, node-positive disease had a nonstatistically significant reduced HR (n = 340; HR, 0.72; 95% CI, 0.49 to 1.05). Seventy-one (13%) of 542 patients assigned to CM maintenance did not start CM. Of 473 patients who received at least one CM maintenance dose (including two patients assigned to no CM), 64 (14%) experienced a grade 3 or 4 treatment-related adverse event; elevated serum transaminases was the most frequently reported (7%), followed by leukopenia (2%). Conclusion: CM maintenance did not produce a significant reduction in DFS events in hormone receptor-negative early breast cancer. The trend toward benefit observed in the TN, node-positive subgroup supports additional exploration of this strategy in the TN, higher-risk population.application/pdf10.1200/JCO.2015.65.6595https://repositorio.inen.sld.pe/handle/inen/118engJ Clin OncolUSAmerican Society of Clinical Oncologyinfo:eu-repo/semantics/openAccessdc.rights.uri: https//creativecomons.org/licenses/by/4.0/https://purl.org/pe-repo/ocde/ford#3.02.21Low-Dose Oral Cyclophosphamide and Methotrexate Maintenance for Hormone Receptor-Negative Early Breast Cancer: International Breast Cancer Study Group Trial 22-00info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionreponame:INEN-Institucionalinstname:Instituto Nacional de Enfermedades Neoplásicasinstacron:INENPublicationORIGINALMarco Colleoni 2016.pdfapplication/pdf1007850https://repositorio.inen.sld.pe/bitstreams/9a3c7c0f-d2b5-4d4f-9bd0-4c2e43ce82de/downloadfc2f395548ad408e7681b6f9e1085efdMD51TEXTMarco Colleoni 2016.pdf.txtMarco Colleoni 2016.pdf.txtExtracted texttext/plain48312https://repositorio.inen.sld.pe/bitstreams/45e35e83-0e24-40f0-8635-6398550ffa26/downloadde39625e06199570e67ff9cabca6555dMD52THUMBNAILMarco Colleoni 2016.pdf.jpgMarco Colleoni 2016.pdf.jpgGenerated Thumbnailimage/jpeg5946https://repositorio.inen.sld.pe/bitstreams/abf9dd8e-2d32-46be-9d90-0f20edc22dcf/downloadc67f2114f6bed6e0c75ca054d7de4aeeMD53inen/118oai:repositorio.inen.sld.pe:inen/1182024-10-24 03:00:23.289dc.rights.uri: https//creativecomons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttps://repositorio.inen.sld.peRepositorio INENrepositorioinendspace@gmail.com |
dc.title.none.fl_str_mv |
Low-Dose Oral Cyclophosphamide and Methotrexate Maintenance for Hormone Receptor-Negative Early Breast Cancer: International Breast Cancer Study Group Trial 22-00 |
title |
Low-Dose Oral Cyclophosphamide and Methotrexate Maintenance for Hormone Receptor-Negative Early Breast Cancer: International Breast Cancer Study Group Trial 22-00 |
spellingShingle |
Low-Dose Oral Cyclophosphamide and Methotrexate Maintenance for Hormone Receptor-Negative Early Breast Cancer: International Breast Cancer Study Group Trial 22-00 Colleoni, M https://purl.org/pe-repo/ocde/ford#3.02.21 |
title_short |
Low-Dose Oral Cyclophosphamide and Methotrexate Maintenance for Hormone Receptor-Negative Early Breast Cancer: International Breast Cancer Study Group Trial 22-00 |
title_full |
Low-Dose Oral Cyclophosphamide and Methotrexate Maintenance for Hormone Receptor-Negative Early Breast Cancer: International Breast Cancer Study Group Trial 22-00 |
title_fullStr |
Low-Dose Oral Cyclophosphamide and Methotrexate Maintenance for Hormone Receptor-Negative Early Breast Cancer: International Breast Cancer Study Group Trial 22-00 |
title_full_unstemmed |
Low-Dose Oral Cyclophosphamide and Methotrexate Maintenance for Hormone Receptor-Negative Early Breast Cancer: International Breast Cancer Study Group Trial 22-00 |
title_sort |
Low-Dose Oral Cyclophosphamide and Methotrexate Maintenance for Hormone Receptor-Negative Early Breast Cancer: International Breast Cancer Study Group Trial 22-00 |
author |
Colleoni, M |
author_facet |
Colleoni, M Gray, KP Gelber,S Láng, I Thürlimann, B Gianni, L Abdi, EA Gomez, HL inderholm, BK Puglis,i F Tondini, C Kralidis, E Eniu, A Cagossi, K Rauch, D Chirgwin, J Gelber, RD Regan, MM Coates, AS Price, KN Viale, G Goldhirsch, A |
author_role |
author |
author2 |
Gray, KP Gelber,S Láng, I Thürlimann, B Gianni, L Abdi, EA Gomez, HL inderholm, BK Puglis,i F Tondini, C Kralidis, E Eniu, A Cagossi, K Rauch, D Chirgwin, J Gelber, RD Regan, MM Coates, AS Price, KN Viale, G Goldhirsch, A |
author2_role |
author author author author author author author author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Colleoni, M Gray, KP Gelber,S Láng, I Thürlimann, B Gianni, L Abdi, EA Gomez, HL inderholm, BK Puglis,i F Tondini, C Kralidis, E Eniu, A Cagossi, K Rauch, D Chirgwin, J Gelber, RD Regan, MM Coates, AS Price, KN Viale, G Goldhirsch, A |
dc.subject.ocde.none.fl_str_mv |
https://purl.org/pe-repo/ocde/ford#3.02.21 |
topic |
https://purl.org/pe-repo/ocde/ford#3.02.21 |
description |
Purpose: To evaluate the benefit of low-dose cyclophosphamide and methotrexate (CM) maintenance, which previously demonstrated antitumor activity and few adverse effects in advanced breast cancer, in early breast cancer. Patients and methods: International Breast Cancer Study Group (IBCSG) Trial 22-00, a randomized phase III clinical trial, enrolled 1,086 women (1,081 intent-to-treat) from November 2000 to December 2012. Women with estrogen receptor- and progesterone receptor-negative (< 10% positive cells by immunohistochemistry) early breast cancer any nodal and human epidermal growth factor receptor 2 status, were randomly assigned anytime between primary surgery and 56 days after the first day of last course of adjuvant chemotherapy to CM maintenance (cyclophosphamide 50 mg/day orally continuously and methotrexate 2.5 mg twice/day orally on days 1 and 2 of every week for 1 year) or to no CM. The primary end point was disease-free survival (DFS), which included invasive recurrences, second (breast and nonbreast) malignancies, and deaths. Results: After a median of 6.9 years of follow-up, DFS was not significantly better for patients assigned to CM maintenance compared with patients assigned to no CM, both overall (hazard ratio [HR], 0.84; 95% CI, 0.66 to 1.06;P = .14) and in triple-negative (TN) disease (n = 814; HR, 0.80; 95% CI, 0.60 to 1.06). Patients with TN, node-positive disease had a nonstatistically significant reduced HR (n = 340; HR, 0.72; 95% CI, 0.49 to 1.05). Seventy-one (13%) of 542 patients assigned to CM maintenance did not start CM. Of 473 patients who received at least one CM maintenance dose (including two patients assigned to no CM), 64 (14%) experienced a grade 3 or 4 treatment-related adverse event; elevated serum transaminases was the most frequently reported (7%), followed by leukopenia (2%). Conclusion: CM maintenance did not produce a significant reduction in DFS events in hormone receptor-negative early breast cancer. The trend toward benefit observed in the TN, node-positive subgroup supports additional exploration of this strategy in the TN, higher-risk population. |
publishDate |
2017 |
dc.date.accessioned.none.fl_str_mv |
2024-07-01T16:28:50Z |
dc.date.available.none.fl_str_mv |
2024-07-01T16:28:50Z |
dc.date.issued.fl_str_mv |
2017 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.version.none.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.doi.none.fl_str_mv |
10.1200/JCO.2015.65.6595 |
dc.identifier.uri.none.fl_str_mv |
https://repositorio.inen.sld.pe/handle/inen/118 |
identifier_str_mv |
10.1200/JCO.2015.65.6595 |
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https://repositorio.inen.sld.pe/handle/inen/118 |
dc.language.iso.none.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.none.fl_str_mv |
American Society of Clinical Oncology |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess |
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dc.rights.uri: https//creativecomons.org/licenses/by/4.0/ |
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dc.rights.uri: https//creativecomons.org/licenses/by/4.0/ |
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application/pdf |
dc.publisher.none.fl_str_mv |
J Clin Oncol |
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US |
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J Clin Oncol |
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