2011
DOI: 10.1200/jco.2011.29.15_suppl.1126
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Phase II trial combining nab-paclitaxel (NP), gemcitabine (G), and bevacizumab (B) in patients (pts) with metastatic breast cancer (MBC): NCCTG N0735.

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Cited by 8 publications
(5 citation statements)
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“…However, the primary endpoint PFS was 39.7 weeks, a result which is consistent with two similar studies that showed PFS of 41.7 weeks [29] and 47.9 weeks [30]. The trial performed by Northfelt et al met its prespecified endpoint of 6 months PFS > 60% and its toxicities were manageable [23]. The trial performed by Halmilton showed PFS of 9.2 months in comparison to a similar study with PFS of 6.1 months [37,38], and also described a favorable rate of febrile neutropenia (3%) and neuropathy (6% grade 3, no grade 4) in comparison to historical control treatments [24].…”
Section: Discussionsupporting
confidence: 74%
See 1 more Smart Citation
“…However, the primary endpoint PFS was 39.7 weeks, a result which is consistent with two similar studies that showed PFS of 41.7 weeks [29] and 47.9 weeks [30]. The trial performed by Northfelt et al met its prespecified endpoint of 6 months PFS > 60% and its toxicities were manageable [23]. The trial performed by Halmilton showed PFS of 9.2 months in comparison to a similar study with PFS of 6.1 months [37,38], and also described a favorable rate of febrile neutropenia (3%) and neuropathy (6% grade 3, no grade 4) in comparison to historical control treatments [24].…”
Section: Discussionsupporting
confidence: 74%
“…The most common adverse effects were neutropenia, fatigue, thrombocytopenia, anemia, leukopenia, and dyspnea. This regimen should be further evaluated in regimens of chemotherapy plus targeted agents in metastatic breast cancer [23]. Another phase II study was performed by Hamilton et al to evaluate the efficacy of treatment with abraxane plus carboplatin plus bevacizumab in 41 women with TNMBC.…”
Section: Nanoparticle Albumin-stabilized Paclitaxelmentioning
confidence: 99%
“…The most common grade 3/4 adverse event was neutropenia with 71%. Neuropathy grade 3 occurred in 4 (8%) patients [20].…”
Section: Weekly Administration Of Nab-paclitaxel As Single Agent In Mbcmentioning
confidence: 99%
“…Nab-paclitaxel combinations at a dose of 125 mg/m 2 with capecitabine and gemcitabine were feasible, safe and active [15,16]. Triple combinations of a biological and 2 cytotoxic agents as first-line treatment were tested with the 125 mg/m 2 dose plus gemcitabine and the 100 mg/m 2 dose with carboplatin, and proved active and manageable [19,20,22]. For most physicians involved in the care of patients with pretreated MBC, a weekly schedule of nab-paclitaxel might be the preferred choice because it allows them to monitor treatment closely and to react promptly to the onset of side effects such as neuropathy.…”
Section: Weekly Administration Of Nab-paclitaxel As Single Agent In Mbcmentioning
confidence: 99%
“…The following supporting information can be downloaded at: , Table S1: the current nanopharmaceuticals for cancer therapy in clinical assays [ 162 , 163 , 164 , 165 , 166 , 167 , 168 , 169 , 170 , 171 , 172 , 173 , 174 , 175 , 176 , 177 , 178 , 179 , 180 , 181 , 182 , 183 , 184 , 185 , 186 , 187 , 188 , 189 , 190 , 191 , 192 , 193 , 194 , 195 , 196 , 197 , 198 , 199 , 200 , 201 , 202 , 203 , 204 , 205 , 206 , 207 , 208 , 209 , 210 ].…”
mentioning
confidence: 99%