Dataset Information

High-dose tamoxifen in high-hormone-receptor-expressing advanced breast cancer patients: a phase II pilot study

ABSTRACT:

Background:

Tumor progression following endocrine therapy is considered to indicate resistance to endocrine drugs due to a variety of mechanisms. An insufficient dose of endocrine drugs is one of the causes for treatment failure in some patients with high hormone-receptor (HR)-expressing advanced breast cancer. This study aimed to explore the efficacy of high-dose tamoxifen (TAM) treatment in patients with advanced breast cancer with highly expressed HR.

Materials & methods:

This was a single-arm, phase?II pilot study that enrolled patients with advanced breast cancer with high HR expression (estrogen receptor ?60% and/or progesterone receptor ?60%) following routine endocrine therapy. All enrolled patients received a high-dose of TAM (100?mg/day) until disease progression. The primary endpoint was progression-free survival (PFS). The secondary endpoints included objective response rate (ORR), clinical benefit rate (CBR), overall survival (OS), and safety. Exploratory endpoints included the predictive value of 16?-18F-17?-fluoroestradiol quantitative positron emission tomography/computed tomography (18F-FES PET/CT) for treatment efficacy.

Results:

A total of 30 patients were enrolled between September 2017 and February 2019. The median PFS was 6?months [95% confidence interval (CI) 4.9–7.1] and the median OS was 15.6?months (95% CI 8.3–22.9). Five patients experienced a partial response (PR) and none experienced a complete response (CR), with an ORR of 16.7% and CBR of 33.3%. No severe adverse events were observed. Lesions with 18F-FES maximum standardized uptake value (SUVmax) ?4 had a significantly longer PFS [median 9.2?months, (95% CI 6.9–11.6)] compared with lesions with a 18F-FES SUVmax <4 [median 4.8?months, (95% CI 3.9–5.6); p?=?0.022].

Conclusion:

A high-dose of TAM is effective and safe for patients with advanced breast cancer with high HR expression. 18F-FES SUVmax values may predict the local clinical benefits of high-dose TAM .

Trial Registration:

[ClinicalTrials.gov identifier: NCT0304565]

SUBMITTER: Su Y

PROVIDER: S-EPMC7934038 | biostudies-literature |

REPOSITORIES: biostudies-literature

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