Toxicity of initial chemotherapy in older patients with lung cancers

被引:15
作者
Zauderer, Marjorie G. [1 ]
Sima, Camelia S. [2 ]
Korc-Grodzicki, Beatriz [3 ]
Kris, Mark G. [1 ]
Krug, Lee M. [1 ]
机构
[1] Weill Cornell Med Coll, Mem Sloan Kettering Canc Ctr, Dept Med, Thorac Oncol Serv, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY 10021 USA
[3] Weill Cornell Med Coll, Mem Sloan Kettering Canc Ctr, Dept Med, Geriatr Serv, New York, NY 10065 USA
关键词
Elderly; Chemotherapy toxicity; Lung cancers; Geriatric assessment; COMPREHENSIVE GERIATRIC ASSESSMENT; ELDERLY-PATIENTS; ADJUVANT CHEMOTHERAPY; ONCOLOGY; TRIAL; VALIDATION; CISPLATIN; OUTCOMES; THERAPY; ADULTS;
D O I
10.1016/j.jgo.2012.09.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: Despite the growing number of elderly patients with lung cancers, we lack adequate information about how best to treat them. A phase III trial demonstrated a survival benefit of doublet chemotherapy in elderly patients with lung cancers compared to single agents at the cost of increased toxicity. We undertook this study to identify and describe chemotherapy-associated toxicity patterns among elderly patients treated for lung cancers. Materials and methods: We reviewed records of patients age 70 or older with metastatic lung cancers who received initial chemotherapy at the Memorial Sloan-Kettering Cancer Center during 2008 and 2009. Results: We identified 70 patients: 28 (40%) completed at least 4 cycles of chemotherapy without dose reduction but 31 (44%) required hospitalization for toxicity. Baseline albumin <3.5 g/dL and anemia were associated with grade 3-5 chemotherapy-associated toxicity. Also, an increase in platelets from cycle 1 to cycle 2 was associated with chemotherapy-associated toxicity. No other statistically significant associations between chemotherapy-associated toxicity and putative biologic and functional risk factors, including age and performance status, were identified. Conclusion: Patients deemed eligible for chemotherapy by their physicians were just as likely to have severe chemotherapy-associated toxicity requiring hospitalization as to finish an initial course of therapy without any serious problems. An increase in platelet count from cycle 1 to cycle 2 was associated with increased toxicity. Additional research, such as exploration of inflammatory cytokines (PDGF, IL6, and IGF-1) to identify the mechanisms of chemotherapy tolerance and prospective evaluation and validation of existing metrics, is needed so that all patients can be appropriately risk stratified. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:64 / 70
页数:7
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