Chemotoxicity recurrence in older patients: Risk factors and effectiveness of preventive strategies-a prospective study

被引:21
作者
Extermann, Martine [1 ,2 ]
Reich, Richard R. [1 ,3 ]
Sehovic, Marina [1 ]
机构
[1] Univ S Florida, Coll Med, H Lee Moffitt Canc Ctr & Res Inst, Oncol Program, Tampa, FL 33612 USA
[2] Univ S Florida, Dept Oncol Sci, Tampa, FL 33612 USA
[3] Univ South Florida Sarasota Manatee, Coll Arts & Sci, Dept Psychol, Sarasota, FL USA
基金
美国国家卫生研究院;
关键词
chemotherapy; elderly; chemotherapy toxicity; management of chemotherapy toxicity; MAX2; index; geriatric oncology; functional status; quality of life; Common Terminology Criteria for Adverse Events (CTCAE); COLONY-STIMULATING FACTOR; CHEMOTHERAPY TOXICITY; ADJUVANT CHEMOTHERAPY; CANCER-PATIENTS; NEUTROPENIA; VALIDATION; ILLNESS; INDEX;
D O I
10.1002/cncr.29423
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
BACKGROUNDThe National Cancer Institute's Common Terminology Criteria for Adverse Events (CTCAE) and adjustment rules after severe toxicity are derived by consensus, but to the authors' knowledge little is known regarding the determinants of toxicity recurrence, especially in the elderly. METHODSThe authors prospectively accrued 200 patients (aged 65 years) before chemotherapy. For those with CTCAE grade 3 to 4 nonhematologic or CTCAE grade 4 hematologic toxicities (severe toxicity), the duration and functional impact, treatment modifications, and severe toxicity recurrence were recorded. The regimen's toxicity was adjusted with the MAX2 index, the average of the most frequent grade 4 hematologic toxicities and the most frequent grade 3 to 4 nonhematologic toxicities reported in publications of a regimen. RESULTSThe median patient age was 73 years (range, 65-90 years). Among 163 patients who were evaluable for toxicity after 1 treatment cycle (receiving on average 4.73 cycles), 82 had severe toxicity, 10 were discontinued for toxicity, 6 were discontinued for other reasons, and 5 patients had died. Sixty-one patients received further chemotherapy: 41 without dose modification (16 with secondary prevention measures) and 20 with dose modifications. Without modification, 19 patients (46%) experienced toxicity recurrence (0 deaths). With modification, 7 patients (35%) experienced a toxicity recurrence (1 death). On univariate analysis, treatment intent, hospitalization, duration-adjusted activities of daily living (ADL), quality of life impact, and fatigue were associated with dose modification. ADL remained associated on multivariate analysis (P=.02). On univariate analysis for toxicity recurrence, Eastern Cooperative Oncology Group performance status and MAX2 score demonstrated an association, with only the latter found to remain statistically significant on multivariate analysis (P=.04). CONCLUSIONSIf a severe toxicity does not have a long duration of impact on ADL, oncologists are less inclined to modify treatment. With proper supportive measures, this leads to recurrence risks similar to those shown in patients with modified treatment, with low risks of toxic deaths overall. Cancer 2015;121:2984-2992. (c) 2015 American Cancer Society. \
引用
收藏
页码:2984 / 2992
页数:9
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