Nab-paclitaxel in older patients with non-small cell lung cancer who have developed disease progression after platinum-based doublet chemotherapy

被引:22
作者
Weiss, Jared M. [1 ]
Pennell, Nathan [2 ]
Deal, Allison M. [1 ]
Morgenzstern, Daniel [3 ]
Bradford, Daniel S. [4 ]
Crane, Jeffrey [5 ]
West, Howard Jack [6 ]
Lee, Carrie [1 ]
Pecot, Chad [1 ]
Stevenson, James P. [2 ]
Irvin, William [7 ]
Socinski, Mark [8 ]
Stinchcombe, Tom [9 ]
Villaruz, Liza C. [10 ]
Muss, Hyman B. [1 ]
机构
[1] Univ North Carolina Chapel Hill, Lineberger Comprehens Canc Ctr, Dept Hematol & Oncol, 170 Manning Dr,Room 3115,Campus Box 7305, Chapel Hill, NC 27514 USA
[2] Cleveland Clin, Hematol & Med Oncol, Cleveland, OH 44106 USA
[3] Washington Univ, Sch Med, Dept Med, Oncol Div, St Louis, MO 63110 USA
[4] Highlands Oncol, Fayetteville, AR USA
[5] Rex Hematol Oncol Associates, Raleigh, NC USA
[6] Swedish Canc Inst, Dept Med Oncol, Seattle, WA USA
[7] Bon Secours, Med Oncol, Midlothian, VA USA
[8] Florida Hosp, Canc Inst, Orlando, FL USA
[9] Duke Univ, Sch Med, Duke Canc Inst, Div Med Oncol, Durham, NC USA
[10] Univ Pittsburgh, Med Ctr, Hillman Canc Ctr, Div Hematol Oncol, Pittsburgh, PA USA
关键词
elderly; geriatric assessment; lymphocyte p16; nanoparticle albumin-bound (nab)-paclitaxel; non-small cell lung cancer (NSCLC); sarcopenia; PHASE-III; GERIATRIC ASSESSMENT; ELDERLY-PATIENTS; SINGLE-AGENT; ADULTS; DOCETAXEL; COMBINATION; CARBOPLATIN; P16(INK4A); SARCOPENIA;
D O I
10.1002/cncr.32573
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The selection of later-line treatment for older patients with AJCC (version 7) stage IV non-small cell lung cancer (NSCLC) remains controversial. Nanoparticle albumin-bound (nab)-paclitaxel is approved with carboplatin for the first-line treatment of patients with NSCLC and subgroup analysis of phase 3 data has suggested superior survival in older patients. Methods The authors conducted a phase 2 study of nab-paclitaxel in 42 patients aged >= 70 years who had been treated previously with a platinum doublet regimen; patients also could have received a PD-1 inhibitor. The primary endpoint of the current study was grade 3 to 5 toxicity (according to the National Cancer Institute Common Terminology Criteria for Adverse Events [version 4.0]). In addition to response rate, progression-free survival (PFS), and overall survival (OS), geriatric assessments also were performed before and during treatment, associations between baseline sarcopenia and outcomes were explored, and changes in T lymphocyte p16 before and during treatment were measured. The authors also performed a retrospective subgroup analysis of 19 older patients who were treated with nab-paclitaxel as part of a larger, randomized, phase 2 study; data were not combined. Results The rate of grade 3 to 5 toxicities was 33.7%. The most common grade 3 to 5 toxicities were decreased white blood cell count (11.9%), neutropenia (9.5%), and fatigue (11.9%). The response rate was 34.2% (2.6% complete response rate and 31.6% partial response rate). The median PFS was 5.2 months and the median OS was 9.3 months. Adverse prognostic factors were common: 42% of patients were frail and 39% of patients were prefrail, whereas 21% had an Eastern Cooperative Oncology Group performance status of 2 and 27% were sarcopenic. Only frailty was found to be predictive of inferior survival. A subgroup analysis of 19 older patients treated with nab-paclitaxel alone in a prior trial demonstrated a response rate of 15.8%, a PFS of 4.2 months, and an OS of 13.6 months. Conclusions Fit and prefrail older patients with stage IV NSCLC should be considered for treatment with nab-paclitaxel after disease progression with doublet chemotherapy.
引用
收藏
页码:1060 / 1067
页数:8
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