4.5 Article

Meta-analysis of nanoparticle albumin-bound paclitaxel used as neoadjuvant chemotherapy for operable breast cancer based on individual patient data (JBCRG-S01 study)

Journal

BREAST CANCER
Volume 28, Issue 5, Pages 1023-1037

Publisher

SPRINGER JAPAN KK
DOI: 10.1007/s12282-021-01238-9

Keywords

Nanoparticle albumin-bound paclitaxel; Meta-analysis; Individual patient data; Pathological complete response; HER2-rich

Funding

  1. Japan Breast Cancer Research Group (JBCRG)
  2. Taiho Pharmaceutical Co., Ltd.

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This study analyzed 16 studies involving 753 patients to investigate the efficacy and safety of nanoparticle albumin-bound paclitaxel (nab-PTX) as neoadjuvant chemotherapy for breast cancer. Results showed that nab-PTX is a safe and acceptable option, particularly for aggressive cancers. Factors such as HER2 positivity, TNBC, high Ki-67, high nuclear grade, and weekly administration of nab-PTX were significantly associated with pathological complete response.
Background Nanoparticle albumin-bound paclitaxel (nab-PTX), a novel taxane formulation, was developed to avoid cremophor/ethanol-associated toxicities including peripheral neuropathy and hypersensitivity. At least 35 phase II studies using combined nab-PTX and anthracycline in neoadjuvant settings are registered in Japan. We analyzed the efficacy and safety of nab-PTX based on patient characteristics in these studies. Methods We conducted a meta-analysis using individual patient data (IPD) to investigate the average efficacy of nab-PTX-containing regimens as neoadjuvant chemotherapy for operable breast cancer. IPD were provided by principal investigators who agreed to participate. The primary endpoint was pathological complete response (pCR) rate of each breast cancer subtype. Results We analyzed the data of 16 studies involving 753 patients. The overall crude frequencies of pCR (ypT0 ypN0, ypT0/is ypN0, and ypT0/is ypNX) were 18.1, 26.0, and 28.6%, respectively. Specifically, the frequencies were 6.7, 10.2, and 13.4% for luminal (n = 343); 40.5, 63.5, and 68.9% for human epidermal growth factor receptor 2 (HER2)-rich, (n = 74); 21.9, 40.6, and 42.7% for luminal/HER2 (n = 96); and 26.3, 31.5, and 32.3% for triple-negative breast cancers (TNBC) (n = 232). The multivariate analyses indicated that HER2 positivity, TNBC, high Ki-67, high nuclear grade, and weekly nab-PTX administration were significantly associated with the pCR. The proportion of hematological toxicities (neutropenia (39.7%) and leukopenia (22.5%)), peripheral sensory neuropathy (9.7%), myalgia (5.7%), and arthralgia (4.7%) was higher than grade 3 adverse events, but most patients recovered. Conclusions Nab-PTX is a safe and acceptable chemotherapeutic agent in neoadjuvant settings, particularly for aggressive cancers. UMIN-CTR#: UMIN000028774

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