Conley Anthony Paul, Guérin Annie, Sasane Medha, Gauthier Geneviève, Schwiep Frances, Keir Christopher Hunt, Wu Eric Q
Department of Sarcoma, Moffitt Cancer Center, 12902 Magnolia Drive, Tampa, FL, USA.
J Gastrointest Cancer. 2013 Jun;44(2):190-8. doi: 10.1007/s12029-012-9467-1.
To compare characteristics of patients, the risk of recurrence, and mortality among adult patients with primary resectable gastrointestinal stromal tumor (GIST) receiving short-term (6-12 months) versus long-term (≥ 24 months) imatinib therapy.
Detailed information on primary resectable KIT-positive GIST patients initiated on imatinib adjuvant therapy was retrospectively collected for short- and long-term imatinib patients from 318 US oncologists using an online data collection form. Patient characteristics were compared using Wilcoxon and Chi-square tests. Disease recurrence and mortality rates were compared using multivariate Cox proportional hazard models.
Among the 406 short-term and 406 long-term imatinib patients, the median follow-up was 916 and 970 days, respectively. While patients generally had similar demographic characteristics, the short-term group had a higher prevalence of cardiovascular and ischemic heart diseases and patients in the long-term group had a higher pre-surgery risk profile. This finding was consistent with the main reason reported by oncologists for prescribing adjuvant imatinib over longer duration, i.e., patient risk profile. Disease recurrence [5.9 versus 1.2 %, (p < .001)] and mortality rates [7.1 % versus 2.0 %, (p < .001)] were higher in short- versus long-term patients. The adjusted risk of recurrence was 5.30 times (p < .001) higher, and mortality risk was 4.02 times (p < .001) higher in short- versus long-term patients.
Patient risk profile is an important factor in oncologists' decisions to prescribe adjuvant imatinib. Despite the higher risk profile observed in long-term patients, the long-term use of imatinib was associated with a reduction in long-term risk of disease recurrence and mortality.
比较接受短期(6 - 12个月)与长期(≥24个月)伊马替尼治疗的原发性可切除胃肠道间质瘤(GIST)成年患者的特征、复发风险和死亡率。
通过在线数据收集表,从318名美国肿瘤学家处回顾性收集了接受伊马替尼辅助治疗的原发性可切除KIT阳性GIST患者的详细信息,这些患者被分为短期和长期伊马替尼治疗组。使用Wilcoxon检验和卡方检验比较患者特征。使用多变量Cox比例风险模型比较疾病复发率和死亡率。
在406名短期和406名长期伊马替尼治疗患者中,中位随访时间分别为916天和970天。虽然患者总体上具有相似的人口统计学特征,但短期治疗组心血管疾病和缺血性心脏病的患病率较高,而长期治疗组患者术前风险状况较高。这一发现与肿瘤学家报告的长期使用辅助伊马替尼的主要原因一致,即患者风险状况。短期治疗患者的疾病复发率[5.9%对1.2%,(p <.001)]和死亡率[7.1%对2.0%,(p <.001)]高于长期治疗患者。短期治疗患者与长期治疗患者相比,调整后的复发风险高5.30倍(p <.001),死亡风险高4.02倍(p <.001)。
患者风险状况是肿瘤学家决定开具辅助伊马替尼处方的重要因素。尽管长期治疗患者的风险状况较高,但长期使用伊马替尼与降低疾病复发和死亡的长期风险相关。