Weekly nab-Paclitaxel in Combination With Carboplatin Versus Solvent-Based Paclitaxel Plus Carboplatin as First-Line Therapy in Patients With Advanced Non-Small-Cell Lung Cancer: Final Results of a Phase III Trial
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作者:
Socinski, Mark A.
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Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USAUniv N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Socinski, Mark A.
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Bondarenko, Igor
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City Hosp 4, Dnepropetrovsk, UkraineUniv N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Bondarenko, Igor
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Karaseva, Nina A.
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City Oncol Ctr, St Petersburg, RussiaUniv N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Karaseva, Nina A.
[4
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Makhson, Anatoly M.
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City Oncol Hosp 62, Moscow, RussiaUniv N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Makhson, Anatoly M.
[5
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Vynnychenko, Igor
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Reg Oncol Ctr, Sumy, UkraineUniv N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Vynnychenko, Igor
[3
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Okamoto, Isamu
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Kinki Univ, Fac Med, Osaka, JapanUniv N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Okamoto, Isamu
[6
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Hon, Jeremy K.
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Clearview Canc Inst, Huntsville, AL USAUniv N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Hon, Jeremy K.
[7
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Hirsh, Vera
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McGill Univ, Montreal, PQ, CanadaUniv N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Hirsh, Vera
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Bhar, Paul
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Celgene, Summit, NJ USAUniv N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Bhar, Paul
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Zhang, Hui
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Celgene, Summit, NJ USAUniv N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Zhang, Hui
[9
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Iglesias, Jose L.
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Celgene, Summit, NJ USAUniv N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Iglesias, Jose L.
[9
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Renschler, Markus F.
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Celgene, Summit, NJ USAUniv N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Renschler, Markus F.
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机构:
[1] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
Purpose This phase III trial compared the efficacy and safety of albumin-bound paclitaxel (nab-paclitaxel) plus carboplatin with solvent-based paclitaxel (sb-paclitaxel) plus carboplatin in advanced non-small-cell lung cancer (NSCLC). Patients and Methods In all, 1,052 untreated patients with stage IIIB to IV NSCLC were randomly assigned 1:1 to receive 100 mg/m(2) nab-paclitaxel weekly and carboplatin at area under the concentration-time curve (AUC) 6 once every 3 weeks (nab-PC) or 200 mg/m2 sb-paclitaxel plus carboplatin AUC 6 once every 3 weeks (sb-PC). The primary end point was objective overall response rate (ORR). Results On the basis of independent assessment, nab-PC demonstrated a significantly higher ORR than sb-PC (33% v 25%; response rate ratio, 1.313; 95% CI, 1.082 to 1.593; P = .005) and in patients with squamous histology (41% v 24%; response rate ratio, 1.680; 95% CI, 1.271 to 2.221; P < .001). nab-PC was as effective as sb-PC in patients with nonsquamous histology (ORR, 26% v 25%; P = .808). There was an approximately 10% improvement in progression-free survival (median, 6.3 v 5.8 months; hazard ratio [HR], 0.902; 95% CI, 0.767 to 1.060; P = .214) and overall survival (OS; median, 12.1 v 11.2 months; HR, 0.922; 95% CI, 0.797 to 1.066; P = .271) in the nab-PC arm versus the sb-PC arm, respectively. Patients >= 70 years old and those enrolled in North America showed a significantly increased OS with nab-PC versus sb-PC. Significantly less grade >= 3 neuropathy, neutropenia, arthralgia, and myalgia occurred in the nab-PC arm, and less thrombocytopenia and anemia occurred in the sb-PC arm. Conclusion The administration of nab-PC as first-line therapy in patients with advanced NSCLC was efficacious and resulted in a significantly improved ORR versus sb-PC, achieving the primary end point. nab-PC produced less neuropathy than sb-PC.
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页码:2055 / 2062
页数:8
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