Key result
Nonpegylated liposomal doxorubicin achieved an objective response in 29% of evaluable patients with metastatic breast cancer, with a median progression-free survival of 7 months.
Why the study?
Does nonpegylated liposomal doxorubicin provide clinical efficacy with acceptable cardiotoxicity in patients with metastatic breast cancer?
Cohort (n=63)
Yes
Does nonpegylated liposomal doxorubicin provide clinical efficacy with acceptable cardiotoxicity in patients with metastatic breast cancer?
Nonpegylated liposomal doxorubicin demonstrates clinical activity with a low incidence of reversible cardiotoxicity in both anthracycline-naïve and pretreated patients with metastatic breast cancer.
May support use in select metastatic breast cancer patients; leaves open need for randomized cardiotoxicity comparisons.
BACKGROUND: This study aimed to investigate the use of nonpegylated liposomal doxorubicin (NPLD) in the management of metastatic breast cancer (MBC) within routine UK clinical practice and to assess its efficacy and tolerability. PATIENTS AND METHODS: All patients that received NPLD for MBC at 5 institutions were identified. Clinicopathologic details, echocardiographic data, and toxicities were documented. Response to treatment, outcome, cardiotoxicity, and safety were assessed. RESULTS: 63 patients (median age at NPLD therapy, 53.5 years) who had received NPLD were identified; 18 (29%) were anthracycline-naïve, and 42 (67%) were anthracycline-pretreated (median cumulative dose of epirubicin, 450 mg/m(2)). In 3 cases, prior treatment history was not available. NPLD was most frequently (16 [25%] of 63 patients) administered as first-line chemotherapy (median, third-line; range, 1-9), although it was given later in anthracycline-pretreated patients (median, fourth-line; range, 1-9). Overall, 14 (29%) of 49 evaluable patients achieved an objective response, which increased to 10 (71%) of 14 when NPLD was given first-line (anthracycline-naïve, 8 [100%] of 8; anthracycline-pretreated, 2 [50%] of 4; adjuvant treatment unknown, 2). Median progression-free survival was 7 months (first-line, 18 months, vs. ≥ second-line, 6 months; P = .0066), and median overall survival was 10 months (first-line, 18 months, vs. ≥ second-line, 10 months; P = .0971). Toxicities tended to be grade 1 or 2. Three patients had cardiotoxicity (left ventricular ejection fraction < 50% or a fall of ≥ 10% from baseline), which resolved during treatment. CONCLUSION: NPLD was used in both anthracycline-naïve patients and those with prior exposure. There is evidence of clinical activity in those with prior exposure to anthracyclines, with a low incidence of cardiotoxicity.
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Palmieri et al. (2013) conducted a cohort in metastatic breast cancer (n=63). Nonpegylated liposomal doxorubicin was evaluated on objective response. Nonpegylated liposomal doxorubicin achieved an objective response in 29% of evaluable patients with metastatic breast cancer, with a median progression-free survival of 7 months.
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