Johnson & Johnson Pharmaceutical Services LLC, Malvern, Pennsylvania, USA.
Clin Ther. 2009;31 Pt 2:2416-32. doi: 10.1016/j.clinthera.2009.11.020.
This study was conducted to evaluate data on chemotherapy-associated anemia and thrombocytopenia, and cycle delays in patients with cancer in a community oncology practice.
Data on adult patients (age > or =18 years) with cancer treated in outpatient oncology clinics throughout the United States between 2000 and 2007 were obtained from a large electronic medical records database. All types of cancer were included, although the focus was on solid cancers (ie, lung, breast, ovarian, head and neck, and colorectal cancers). Chemotherapy regimens were grouped from most to least toxic as follows: platinum-based, anthracycline-based, gemcitabine-based, taxane-based, and all other regimens. Anemia (defined as hemoglobin <11 g/dL), thrombocytopenia (defined as platelet count <150 x 10(9)/L), red blood cell (RBC) and platelet transfusions, and use of erythropoietin-stimulating agents (ESAs) were examined by tumor and regimen type. Cycle delays (>7 days) during chemotherapy were also evaluated.
A total of 47,159 patients were included in the study (58.4% female; mean [SD] age, 60.76 [13.9] years). The most common cancer was breast cancer (19.5%), followed by non-small cell lung cancer (14.9%), colorectal cancer (11.9%), ovarian cancer (3.1%), and head and neck cancer (2.5%). At baseline, 20.9% of patients had anemia and 11.1% had thrombocytopenia. A total of 75,243 chemotherapy regimens were administered. During the course of chemotherapy, from 46.4% to 59.0% of patients developed anemia. The prevalence of thrombocytopenia ranged from 21.9% in patients treated with taxane-based regimens to 64.2% in patients treated with gemcitabine-based regimens. In patients from a single hospital-based outpatient center that had the most complete transfusion data (representing 18.3% of the population), the use of RBC transfusion ranged from 4.5% in patients treated with anthracycline-based regimens to 11.6% in patients treated with platinum-based regimens. ESAs were received at some point during chemotherapy by 49.1% of patients. For those with complete dose information, dose delay occurred in 8.2% of chemotherapy cycles; the mean delay was 17 days.
In this study of anemia and thrombocytopenia in a large cohort of patients undergoing chemotherapy for solid tumors in an outpatient oncology clinic in 2000-2007, the burden of anemia and thrombocytopenia remained high.
本研究旨在评估在社区肿瘤学实践中癌症患者化疗相关贫血和血小板减少症以及周期延迟的数据。
从一个大型电子病历数据库中获取了 2000 年至 2007 年间美国各地门诊肿瘤诊所治疗的成年癌症患者(年龄≥18 岁)的数据。包括所有类型的癌症,但重点是实体瘤(即肺癌、乳腺癌、卵巢癌、头颈部癌和结直肠癌)。化疗方案按毒性从高到低分组如下:铂类、蒽环类、吉西他滨类、紫杉烷类和其他所有方案。通过肿瘤和方案类型检查贫血(定义为血红蛋白<11g/dL)、血小板减少症(定义为血小板计数<150×10^9/L)、红细胞(RBC)和血小板输注以及促红细胞生成素刺激剂(ESAs)的使用。还评估了化疗期间>7 天的周期延迟。
共有 47159 例患者纳入研究(58.4%为女性;平均[标准差]年龄为 60.76[13.9]岁)。最常见的癌症是乳腺癌(19.5%),其次是非小细胞肺癌(14.9%)、结直肠癌(11.9%)、卵巢癌(3.1%)和头颈部癌(2.5%)。基线时,20.9%的患者有贫血,11.1%的患者有血小板减少症。共进行了 75243 次化疗方案。在化疗过程中,46.4%至 59.0%的患者出现贫血。血小板减少症的患病率范围从接受紫杉烷类方案治疗的患者的 21.9%到接受吉西他滨类方案治疗的患者的 64.2%。在一家拥有最完整输血数据的单院门诊中心的患者中(占人群的 18.3%),接受红细胞输注的患者比例范围从接受蒽环类方案治疗的患者的 4.5%到接受铂类方案治疗的患者的 11.6%。在接受化疗的患者中,有 49.1%的患者在某个时候接受了 ESAs。对于那些有完整剂量信息的患者,8.2%的化疗周期出现剂量延迟;平均延迟时间为 17 天。
在这项对 2000 年至 2007 年间在门诊肿瘤诊所接受实体瘤化疗的大量患者进行的贫血和血小板减少症研究中,贫血和血小板减少症的负担仍然很高。