Lyman Gary H, Kuderer Nicole, Agboola Olayemi, Balducci Lodovico
James P. Wilmot Cancer Center, University of Rochester Medical Center, NY 14642, USA.
Cancer Control. 2003 Nov-Dec;10(6):487-99. doi: 10.1177/107327480301000607.
Neutropenia and its complications represent the major dose-limiting toxicity of cancer chemotherapy, especially in the elderly. Hematopoietic growth factors have been shown to reduce the severity and duration of febrile neutropenia (FN) and to sustain chemotherapy dose intensity.
A systematic review was undertaken of studies of the relationship between age and the risk of neutropenia and its complications. Recent studies of the "Awareness of Neutropenia in Chemotherapy Study Group" related to the impact of age on neutropenic complications are also summarized.
The risk of FN associated with standard regimens increases with age and appears to be greatest during the first cycle of chemotherapy. FN continues to have a considerable clinical, economic, and quality-of-life impact on affected individuals. The risk of mortality associated with hospitalization with FN also increases with age but is largely associated with the higher rate of comorbidities observed in the elderly population. Despite increasing evidence that elderly patients experience similar benefit from cancer chemotherapy, reductions in dose intensity often compromise response rates and long-term survival. The hematopoietic growth factors reduce the risk of neutropenic events and the need for reduced dose intensity in elderly cancer patients. Primary prophylaxis with colony-stimulating factors (CSFs) reduces the risk of FN and its complications in elderly patients receiving moderately intensive systemic chemotherapy for responsive malignancies. CSFs also appear to reduce cost and improve quality of life in selected elderly patients receiving chemotherapy.
Primary prophylaxis with CSFs should be considered in elderly patients with responsive and potentially curable malignancies who receive moderately intensive chemotherapy.
中性粒细胞减少症及其并发症是癌症化疗的主要剂量限制性毒性反应,在老年患者中尤为如此。造血生长因子已被证明可降低发热性中性粒细胞减少症(FN)的严重程度和持续时间,并维持化疗剂量强度。
对年龄与中性粒细胞减少症及其并发症风险之间关系的研究进行了系统综述。还总结了“化疗中性粒细胞减少症认识研究组”最近关于年龄对中性粒细胞减少症并发症影响的研究。
与标准方案相关的FN风险随年龄增加而增加,且在化疗的第一个周期似乎最高。FN对受影响个体仍有相当大的临床、经济和生活质量影响。与FN住院相关的死亡风险也随年龄增加,但在很大程度上与老年人群中观察到的较高合并症发生率有关。尽管越来越多的证据表明老年患者从癌症化疗中获得相似的益处,但剂量强度的降低往往会影响缓解率和长期生存。造血生长因子可降低老年癌症患者中性粒细胞减少事件的风险以及降低剂量强度的必要性。对于接受中度强度全身化疗以治疗敏感恶性肿瘤的老年患者,使用集落刺激因子(CSF)进行一级预防可降低FN及其并发症的风险。CSF似乎还可降低特定接受化疗的老年患者的成本并改善生活质量。
对于接受中度强度化疗的有敏感且可能治愈的恶性肿瘤的老年患者,应考虑使用CSF进行一级预防。