Lachance D H, Brizel D M, Gockerman J P, Halperin E C, Burger P C, Boyko O B, Brown M T, Schold S C
Division of Neurology, Duke University Medical Center, Durham, NC.
Neurology. 1994 Sep;44(9):1721-7. doi: 10.1212/wnl.44.9.1721.
The activity of cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) in the treatment of primary central nervous system lymphoma (PCNSL) prior to radiotherapy was studied in six patients. Primary lesions were reduced by 80% or more on contrast-enhancing cross-sectional area in four patients and to a lesser extent in two others after two cycles of chemotherapy. The primary lesion sites demonstrated no contrast enhancement in the three patients who completed four cycles of therapy. However, concurrent with response at the primary disease sites, multiple lesions occurred at distant, noncontiguous CNS parenchymal sites in five patients after two to four cycles of chemotherapy. Median survival was 8.5 months for the six enrolled patients and 16.5 months for the four patients completing craniospinal radiotherapy. PCNSL is highly responsive to standard systemic non-Hodgkin's lymphoma chemotherapy regimens, but the pattern and rapidity of relapse suggest mechanisms of failure including inherent or rapidly evolving antineoplastic drug resistance and perhaps limited drug delivery to occult sites of disease in the brain.
对6例患者研究了环磷酰胺、阿霉素、长春新碱和强的松(CHOP)方案在放疗前治疗原发性中枢神经系统淋巴瘤(PCNSL)中的活性。在两个化疗周期后,4例患者的主要病灶在增强扫描截面积上缩小了80%或更多,另外2例缩小程度较小。在完成四个周期治疗的3例患者中,主要病灶部位无强化表现。然而,在主要疾病部位出现缓解的同时,5例患者在两到四个化疗周期后,在远处不连续的中枢神经系统实质部位出现了多个病灶。6例入组患者的中位生存期为8.5个月,4例完成颅脊髓放疗的患者中位生存期为16.5个月。PCNSL对标准的系统性非霍奇金淋巴瘤化疗方案高度敏感,但复发的模式和速度提示存在失败机制,包括内在的或迅速演变的抗肿瘤药物耐药性,以及可能向脑部隐匿病灶的药物递送受限。