Upfront Taxane Could Be Superior to Pegylated Liposomal Doxorubicin (PLD): A Retrospective Real-World Analysis of Treatment Sequence Taxane–PLD versus PLD–Taxane in Patients with Metastatic Breast Cancer

Author:

Wallrabenstein Till12ORCID,Oseledchyk Anton1,Daetwyler Eveline1ORCID,Rochlitz Christoph1,Vetter Marcus134ORCID

Affiliation:

1. University Hospital Basel, Medical Oncology, Petersgraben 4, 4031 Basel, Switzerland

2. University Medical Center Freiburg, Hematology and Oncology, Hugstetter Strasse 55, 79106 Freiburg, Germany

3. Zentrum Onkologie & Hämatologie, Tumorzentrum, Kantonsspital Baselland, Rheinstrasse 26, 4410 Liestal, Switzerland

4. Medical Faculty, University Basel, 4031 Basel, Switzerland

Abstract

Background: Patients with endocrine-resistant metastatic breast cancer (MBC) require cytostatic therapy. Single-agent taxanes and anthracyclines, including pegylated liposomal doxorubicin (PLD), are standard treatment options. There are no prospective data regarding optimal treatment sequences, and real-world data regarding both treatment options are limited. Methods: We analyzed electronic records of all patients with Her2-negative MBC treated with either first-line PLD or first-line taxane and subsequent crossover at the University Hospital Basel between 2003 and 2021. The primary endpoint was time to next chemotherapy or death (TTNC). Secondary endpoints were overall survival (OS), progression-free survival (PFS), and objective response rate (ORR). We used the Kaplan–Meyer method and logrank test to compare time-to-event endpoints and the Fisher exact test to compare discrete variables. Results: We retrospectively identified 42 patients with Her2-negative MBC who have received either single-agent PLD or single-agent taxane as first-line chemotherapy with subsequent crossover, including 23 patients who received first-line PLD and 19 patients who received first-line taxane. Baseline characteristics were similar between treatment groups. Treatment sequence PLD–taxane was significantly inferior to taxane–PLD regarding all endpoints: median TTNC 4.9 vs. 9.9 months (p = 0.006), median OS 17.8 vs. 24.6 months (p = 0.05), median PFS 4.4 vs. 9.0 months (p = 0.005), and ORR 13% vs. 53% (p = 0.01). Conclusions: Here, we report a first retrospective head-to-head comparison of the treatment sequence PLD–taxane versus taxane–PLD in patients with MBC, showing a substantial advantage of using taxanes first, followed by PLD. An inherent treatment bias in favor of first-line taxanes cannot be excluded, thus calling for prospective validation.

Funder

Open Access Publication Fund of the University of Freiburg in financing publication costs

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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