Randomized Phase III Trial of Weekly Compared with Every-3-weeks Paclitaxel for Metastatic Breast Cancer, with Trastuzumab for All HER-2 Overexpressors and Random Assignment to Trastuzumab or Not in HER-2 Nonoverexpressors: Final Results of Cancer...
Overview
Authors
Affiliations
Purpose: Phase II trials suggested that weekly paclitaxel might be more effective and less toxic than every-3-weeks administration for metastatic breast cancer (MBC). Cancer and Leukemia Group B (CALGB) protocol 9840 was initiated to address this question. Subsequently trastuzumab was demonstrated to improve outcomes of paclitaxel therapy for human epidermal growth factor receptor-2 (HER-2)-positive patients, and was therefore incorporated. Because inhibition of HER-family signaling had potential efficacy even without HER-2 overexpression, we randomly assigned for trastuzumab in this population.
Patients And Methods: Patients were randomly assigned to paclitaxel 175 mg/m(2) every 3 weeks or 80 mg/m(2) weekly. After the first 171 patients, all HER-2-positive patients received trastuzumab; HER-2 nonoverexpressors were randomly assigned for trastuzumab, in addition to paclitaxel schedule. A total of 577 patients were treated on 9840. An additional 158 patients were included in analyses, for combined sample of 735. The primary end point was response rate (RR); secondary end points were time to progression (TTP), overall survival, and toxicity. Primary comparisons were between weekly versus every-3-weeks paclitaxel, and trastuzumab versus no trastuzumab in HER-2 nonoverexpressors.
Results: In the combined sample, weekly paclitaxel was superior to every-3-weeks administration: RR (42% v 29%, unadjusted odds ratio [OR] = 1.75; P = .0004), TTP (median, 9 v 5 months; adjusted HR = 1.43; P < .0001), and survival (median, 24 v 12 months; adjusted HR = 1.28; P = .0092). For HER-2 nonoverexpressors, trastuzumab did not improve efficacy. Grade 3 neuropathy was more common with weekly dosing (24% v 12%; P = .0003).
Conclusion: Weekly paclitaxel is more effective than every-3-weeks administration for MBC. Trastuzumab did not improve efficacy for HER-2 nonoverexpressors. Neurotoxicity is a treatment-limiting toxicity for weekly paclitaxel.
Noyan S, Gur Dedeoglu B Balkan Med J. 2025; 42(2):150-156.
PMID: 40033677 PMC: 11881538. DOI: 10.4274/balkanmedj.galenos.2025.2024-12-47.
Pre-treatment amino acids and risk of paclitaxel-induced peripheral neuropathy in SWOG S0221.
Chen C, Zirpoli G, Budd G, Barlow W, Pusztai L, Hortobagyi G Cancer Chemother Pharmacol. 2024; 94(2):311-321.
PMID: 38814343 PMC: 11878155. DOI: 10.1007/s00280-024-04680-6.
Using maximum plasma concentration (C) to personalize taxane treatment and reduce toxicity.
Sun Y, Cheng Y, Hertz D Cancer Chemother Pharmacol. 2024; 93(6):525-539.
PMID: 38734836 DOI: 10.1007/s00280-024-04677-1.
Satheesh C, Taran R, Singh J, Shrivastav S, Vithalani N, Mukherjee K Ther Adv Med Oncol. 2024; 16:17588359241236442.
PMID: 38680290 PMC: 11047258. DOI: 10.1177/17588359241236442.
Hertz D, Joerger M, Bang Y, Mathijssen R, Zhou C, Zhang L Eur J Cancer. 2024; 202:114024.
PMID: 38513383 PMC: 11053297. DOI: 10.1016/j.ejca.2024.114024.