Naito K, Kobayashi M, Oyama A, Kodera Y, Tanaka M, Kamiya O, Mitomo Y, Ohno R, Sampi K, Hirano M
Dept. of Internal Medicine, Branch Hospital of Nagoya University Hospital.
Gan To Kagaku Ryoho. 1988 Jul;15(7):2145-51.
A phase II study of carboplatin for malignant lymphoma was conducted. Thirty-nine patients with malignant lymphoma were entered into this study, and 6 of them were excluded from evaluation due to violation of selection criteria. The remaining 33 cases were studied to assess the effectiveness and safety of this drug. Two CR and 11 PR were obtained with this medication (effective rate 39%). The significant affecting factors were previous treatment, disease stage and P.S. score. Many cases suffered from gastrointestinal symptoms and reduced hematopoiesis. The former complication was self-limited without any fatal episodes. However, the latter included severe cases, especially thrombocytopenia, which is suggested to be a dose limiting factor (DLF) of this drug.
开展了一项关于卡铂治疗恶性淋巴瘤的II期研究。39例恶性淋巴瘤患者进入本研究,其中6例因违反入选标准而被排除在评估之外。对其余33例患者进行研究以评估该药物的有效性和安全性。使用该药物获得了2例完全缓解(CR)和11例部分缓解(PR)(有效率39%)。显著影响因素为既往治疗、疾病分期和体能状态(P.S.)评分。许多病例出现胃肠道症状和造血功能降低。前一种并发症为自限性,无任何致命事件。然而,后一种情况包括严重病例,尤其是血小板减少症,提示这是该药物的剂量限制因素(DLF)。