Glembatumumab vedotin for patients with metastatic, gpNMB overexpressing, triple-negative breast cancer (“METRIC”): a randomized multicenter study
Abstract The METRIC study (NCT#0199733) explored a novel antibody–drug conjugate, glembatumumab vedotin (GV), targeting gpNMB that is overexpressed in ~40% of patients with triple-negative breast cancer (TNBC) and associated with poor prognosis. The study was a randomized, open-label, phase 2b study...
Guardado en:
Autores principales: | , , , , , , , , , , , , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/17180d15d53a444b97cb83ce78fb7480 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:17180d15d53a444b97cb83ce78fb7480 |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:17180d15d53a444b97cb83ce78fb74802021-12-02T17:18:05ZGlembatumumab vedotin for patients with metastatic, gpNMB overexpressing, triple-negative breast cancer (“METRIC”): a randomized multicenter study10.1038/s41523-021-00244-62374-4677https://doaj.org/article/17180d15d53a444b97cb83ce78fb74802021-05-01T00:00:00Zhttps://doi.org/10.1038/s41523-021-00244-6https://doaj.org/toc/2374-4677Abstract The METRIC study (NCT#0199733) explored a novel antibody–drug conjugate, glembatumumab vedotin (GV), targeting gpNMB that is overexpressed in ~40% of patients with triple-negative breast cancer (TNBC) and associated with poor prognosis. The study was a randomized, open-label, phase 2b study that evaluated progression-free survival (PFS) of GV compared with capecitabine in gpNMB-overexpressing TNBC. Patients who had previously received anthracycline and taxane-based therapy were randomized 2:1 to receive, GV (1.88 mg/kg IV q21 days) or capecitabine (2500 mg/m2 PO daily d1–14 q21 days). The primary endpoint was RECIST 1.1 PFS per independent, blinded central review. In all, 327 patients were randomized to GV (213 treated) or capecitabine (92 treated). Median PFS was 2.9 months for GV vs. 2.8 months for capecitabine. The most common grade ≥3 toxicities for GV were neutropenia, rash, and leukopenia, and for capecitabine were fatigue, diarrhea, and palmar-plantar erythrodysesthesia. The study did not meet the primary endpoint of improved PFS over capecitabine or demonstrate a relative risk/benefit improvement over capecitabine.Linda T. VahdatPeter SchmidAndres Forero-TorresKimberly BlackwellMelinda L. TelliMichelle MeliskoVolker MöbusJavier CortesAlberto J. MonteroCynthia MaRita NandaGail S. WrightYi HeThomas HawthorneRebecca G. BagleyAbdel-Baset HalimChristopher D. TurnerDenise A. YardleyNature PortfolioarticleNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENnpj Breast Cancer, Vol 7, Iss 1, Pp 1-10 (2021) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 |
spellingShingle |
Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 Linda T. Vahdat Peter Schmid Andres Forero-Torres Kimberly Blackwell Melinda L. Telli Michelle Melisko Volker Möbus Javier Cortes Alberto J. Montero Cynthia Ma Rita Nanda Gail S. Wright Yi He Thomas Hawthorne Rebecca G. Bagley Abdel-Baset Halim Christopher D. Turner Denise A. Yardley Glembatumumab vedotin for patients with metastatic, gpNMB overexpressing, triple-negative breast cancer (“METRIC”): a randomized multicenter study |
description |
Abstract The METRIC study (NCT#0199733) explored a novel antibody–drug conjugate, glembatumumab vedotin (GV), targeting gpNMB that is overexpressed in ~40% of patients with triple-negative breast cancer (TNBC) and associated with poor prognosis. The study was a randomized, open-label, phase 2b study that evaluated progression-free survival (PFS) of GV compared with capecitabine in gpNMB-overexpressing TNBC. Patients who had previously received anthracycline and taxane-based therapy were randomized 2:1 to receive, GV (1.88 mg/kg IV q21 days) or capecitabine (2500 mg/m2 PO daily d1–14 q21 days). The primary endpoint was RECIST 1.1 PFS per independent, blinded central review. In all, 327 patients were randomized to GV (213 treated) or capecitabine (92 treated). Median PFS was 2.9 months for GV vs. 2.8 months for capecitabine. The most common grade ≥3 toxicities for GV were neutropenia, rash, and leukopenia, and for capecitabine were fatigue, diarrhea, and palmar-plantar erythrodysesthesia. The study did not meet the primary endpoint of improved PFS over capecitabine or demonstrate a relative risk/benefit improvement over capecitabine. |
format |
article |
author |
Linda T. Vahdat Peter Schmid Andres Forero-Torres Kimberly Blackwell Melinda L. Telli Michelle Melisko Volker Möbus Javier Cortes Alberto J. Montero Cynthia Ma Rita Nanda Gail S. Wright Yi He Thomas Hawthorne Rebecca G. Bagley Abdel-Baset Halim Christopher D. Turner Denise A. Yardley |
author_facet |
Linda T. Vahdat Peter Schmid Andres Forero-Torres Kimberly Blackwell Melinda L. Telli Michelle Melisko Volker Möbus Javier Cortes Alberto J. Montero Cynthia Ma Rita Nanda Gail S. Wright Yi He Thomas Hawthorne Rebecca G. Bagley Abdel-Baset Halim Christopher D. Turner Denise A. Yardley |
author_sort |
Linda T. Vahdat |
title |
Glembatumumab vedotin for patients with metastatic, gpNMB overexpressing, triple-negative breast cancer (“METRIC”): a randomized multicenter study |
title_short |
Glembatumumab vedotin for patients with metastatic, gpNMB overexpressing, triple-negative breast cancer (“METRIC”): a randomized multicenter study |
title_full |
Glembatumumab vedotin for patients with metastatic, gpNMB overexpressing, triple-negative breast cancer (“METRIC”): a randomized multicenter study |
title_fullStr |
Glembatumumab vedotin for patients with metastatic, gpNMB overexpressing, triple-negative breast cancer (“METRIC”): a randomized multicenter study |
title_full_unstemmed |
Glembatumumab vedotin for patients with metastatic, gpNMB overexpressing, triple-negative breast cancer (“METRIC”): a randomized multicenter study |
title_sort |
glembatumumab vedotin for patients with metastatic, gpnmb overexpressing, triple-negative breast cancer (“metric”): a randomized multicenter study |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/17180d15d53a444b97cb83ce78fb7480 |
work_keys_str_mv |
AT lindatvahdat glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT peterschmid glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT andresforerotorres glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT kimberlyblackwell glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT melindaltelli glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT michellemelisko glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT volkermobus glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT javiercortes glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT albertojmontero glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT cynthiama glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT ritananda glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT gailswright glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT yihe glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT thomashawthorne glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT rebeccagbagley glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT abdelbasethalim glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT christopherdturner glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy AT deniseayardley glembatumumabvedotinforpatientswithmetastaticgpnmboverexpressingtriplenegativebreastcancermetricarandomizedmulticenterstudy |
_version_ |
1718381129783836672 |