Publications

Detailed Information

A Real-World Efficacy of Nab-Paclitaxel Monotherapy in Metastatic Breast Cancer

DC Field Value Language
dc.contributor.authorKim, Jung Sun-
dc.contributor.authorSuh, Koung Jin-
dc.contributor.authorLee, Dae-Won-
dc.contributor.authorWoo, Go-Un-
dc.contributor.authorKim, Miso-
dc.contributor.authorKim, Se Hyun-
dc.contributor.authorRyu, Han Suk-
dc.contributor.authorLee, Kyung-Hun-
dc.contributor.authorKim, Tae-Yong-
dc.contributor.authorHan, Sae-Won-
dc.contributor.authorPark, So Yeon-
dc.contributor.authorPark, In Ae-
dc.contributor.authorKim, Jee Hyun-
dc.contributor.authorIm, Seock-Ah-
dc.date.accessioned2023-03-20T08:42:29Z-
dc.date.available2023-03-20T08:42:29Z-
dc.date.created2022-05-25-
dc.date.created2022-05-25-
dc.date.created2022-05-25-
dc.date.issued2022-04-
dc.identifier.citationCancer Research and Treatment, Vol.54 No.2, pp.488-496-
dc.identifier.issn1598-2998-
dc.identifier.urihttps://hdl.handle.net/10371/189453-
dc.description.abstractPurpose We aimed to assess the real-world efficacy of nab-paclitaxel in metastatic breast cancer patients. Materials and Methods This is a retrospective study performed in two tertiary referral hospitals in Korea. Patients with metastatic breast cancer treated with nab-paclitaxel (Abraxane) between March 2016 and March 2020 were enrolled. Results A total of 102 patients with metastatic breast cancer were included. Patients were heavily pre-treated with a median of four prior lines of chemotherapy (5 lines when including endocrine therapy in hormone-receptor-positive patients), and 66 patients (64.7%) were exposed to taxanes in the metastatic setting. According to St. Gallen molecular subtypes, 36 patients (35.3%) were luminal A, 28 (27.5%) were luminal B, 18 (17.7%) were human epidermal growth factor receptor 2-positive and 20 (19.6%) had triple-negative disease. Fifty patients (49.0%) were treated with a 3-weekly regimen (260 mg/m(2) on day 1 every 3 weeks), and 52 (51.0%) were treated with a weekly regimen (100 mg/m(2) every week). Objective response rate was 22.9%. After a median follow-up of 22.0 months, median progression-free survival (PFS) was 4.0 months (95% confidence interval [CI], 2.6 to 4.8) and median overall survival was 8.7 months (95% CI, 7.5 to 11.2). Patients treated with weekly regimen had longer PFS compared to 3-weekly regimen (5.5 vs. 2.3 months, p < 0.001). Multivariate analysis revealed the treatment regimen as an independent prognostic factor for PFS. There was no grade 3 or 4 hypersensitivity reaction. Conclusion This real-world data shows that nab-paclitaxel is a reasonable treatment option in heavily pre-treated and/or taxane-exposed metastatic breast cancer patients.-
dc.language영어-
dc.publisher대한암학회-
dc.titleA Real-World Efficacy of Nab-Paclitaxel Monotherapy in Metastatic Breast Cancer-
dc.typeArticle-
dc.identifier.doi10.4143/crt.2021.394-
dc.citation.journaltitleCancer Research and Treatment-
dc.identifier.wosid000789993400017-
dc.identifier.scopusid2-s2.0-85120547574-
dc.citation.endpage496-
dc.citation.number2-
dc.citation.startpage488-
dc.citation.volume54-
dc.identifier.kciidART002830466-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorLee, Dae-Won-
dc.contributor.affiliatedAuthorRyu, Han Suk-
dc.contributor.affiliatedAuthorPark, So Yeon-
dc.contributor.affiliatedAuthorPark, In Ae-
dc.contributor.affiliatedAuthorKim, Jee Hyun-
dc.contributor.affiliatedAuthorIm, Seock-Ah-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusALBUMIN-BOUND PACLITAXEL-
dc.subject.keywordPlusPHASE-III TRIAL-
dc.subject.keywordPlusTHERAPY-
dc.subject.keywordPlusWOMEN-
dc.subject.keywordAuthorAlbumin-bound paclitaxel-
dc.subject.keywordAuthorBreast neoplasms-
dc.subject.keywordAuthorNeoplasm metastasis-
Appears in Collections:
Files in This Item:
There are no files associated with this item.

Related Researcher

  • College of Medicine
  • Department of Medicine
Research Area Clinical Medicine

Altmetrics

Item View & Download Count

  • mendeley

Items in S-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

Share