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Clinical Trial
. 2021 Sep 27;11(1):19154.
doi: 10.1038/s41598-021-98113-6.

Weekly Paclitaxel given concurrently with Durvalumab has a favorable safety profile in triple-negative metastatic breast cancer

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Free PMC article
Clinical Trial

Weekly Paclitaxel given concurrently with Durvalumab has a favorable safety profile in triple-negative metastatic breast cancer

Hazem Ghebeh et al. Sci Rep. .
Free PMC article

Abstract

Therapeutic anti-PD-L1 antibodies are safe as a monotherapy, albeit with minimal efficacy in triple-negative breast cancer (TNBC). This trial aimed to test the safety and efficacy of Durvalumab and Paclitaxel in metastatic TNBC. In this open-label, one-arm trial, five cycles of weekly paclitaxel were delivered intravenously (IV) concurrent with Durvalumab that was given IV every 2 weeks. The combination was preceded by one cycle of paclitaxel alone, for immunological priming, followed by Durvalumab solo until disease progression or unacceptable toxicity. Between 2017 and 2019, 14 patients received at least one cycle of the combination therapy. The therapy was safe with no-dose limiting toxicity, except one case of skin lesions. Adverse events (AEs) were reported in 71% of patients, and there was no death due to the combination therapy. Regardless of grade, the most common AEs were headache and peripheral neuropathy, as each happened in four patients (29%), followed by fatigue and skin rash in three patients (21%) each. Grade 3/4 AEs were experienced by three patients (21%), with the most common being headache and anemia, which happened in two patients (14%). The confirmed objective response rate (ORR) was observed in five patients with a median duration of 10.0 months. Median Progression-free survival (PFS) and overall survival (OS) were 5 and 20.7 months, respectively. The combination of Durvalumab and Paclitaxel is safe, leaving room for additional agents. This is the first report on the combination of Durvalumab and Paclitaxel in the treatment of TNBC (NCT02628132).

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Conflict of interest statement

Dr. Taher Al-Tweigeri has received speaking honoraria from Roche, Novartis, and Lilly. He also received travel support from Roche and Novartis and has served on advisory committees for Roche, Lilly, and Novartis. Dr. Hazem Ghebeh received travel support from AstraZeneca. Other authors declare no potential conflicts of interest.

Figures

Figure 1
Figure 1
Change of tumor burden in patients after starting treatment. Timeline for change in tumor burden (total volume) based on tumor dimensions provided in patients' CT scans. *Patients with confirmed partial or complete response. Tumor burden is followed until discontinuation of therapy (n = 13) or complete response (n = 1).
Figure 2
Figure 2
Progression-free and overall survival of patients. Kaplan–Meier survival curves showing progression-free survival (PFS) and overall survival (OS) of patients.

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