Melchardt Thomas, Weiss Lukas, Hufnagl Clemens, Neureiter Daniel, Kemmerling Ralf, Morre Patrick, Boekstegers Ann, Hopfinger Georg, Auberger Jutta, Steinkirchner Susanne, Pleyer Lisa, Greil Richard, Egle Alexander
Department of Internal Medicine III with Hematology, Medical Oncology, Hemostaseology, Infectious Disease, Rheumatology, Oncologic Center, Laboratory for Immunological and Molecular Cancer Research, Paracelsus Medical University Salzburg , Austria.
Leuk Lymphoma. 2015 Feb;56(2):353-60. doi: 10.3109/10428194.2014.916798. Epub 2014 Jun 25.
Clinical and/or biological risk factors are needed to identify elderly patients with aggressive B-cell lymphoma able to receive full-dose R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone) treatment. We present a retrospective analysis of 83 patients≥75 years of age (range: 75-97) who were diagnosed with aggressive B cell lymphoma between 2004 and 2011 in our clinic. R-CHOP-like therapy was administered in 82% of these patients resulting in a median overall survival of 54 months. A median cumulative dose of 226 mg/m2 doxorubicin and a median of six cycles were applied in these patients. Two genotypes of the CBR3 and MLH1 genes affecting the metabolism of cytostatics identified a subgroup with a favorable prognosis (median overall survival not reached vs. 30 months, p=0.01). A treatment strategy aiming at full-dose R-CHOP was feasible and resulted in an encouraging treatment outcome in patients≥75 years. Pharmacogenetic parameters, if independently validated, may be helpful in elderly patients.
需要临床和/或生物学风险因素来识别能够接受全剂量R-CHOP(利妥昔单抗、环磷酰胺、阿霉素、长春新碱、泼尼松)治疗的侵袭性B细胞淋巴瘤老年患者。我们对2004年至2011年期间在我们诊所诊断为侵袭性B细胞淋巴瘤的83例年龄≥75岁(范围:75-97岁)的患者进行了回顾性分析。这些患者中有82%接受了类似R-CHOP的治疗,中位总生存期为54个月。这些患者应用的阿霉素中位累积剂量为226mg/m²,中位疗程为6个周期。影响细胞抑制剂代谢的CBR3和MLH1基因的两种基因型确定了一个预后良好的亚组(中位总生存期未达到与30个月相比,p=0.01)。针对全剂量R-CHOP的治疗策略是可行的,并且在≥75岁的患者中产生了令人鼓舞的治疗结果。药物遗传学参数如果得到独立验证,可能对老年患者有帮助。