MacEwen E G, Rosenthal R, Matus R, Viau A T, Abuchowski A
Cancer. 1987 Jun 15;59(12):2011-5. doi: 10.1002/1097-0142(19870615)59:12<2011::aid-cncr2820591207>3.0.co;2-m.
Thirty-seven dogs with malignant lymphoma were treated with either polyethylene glycol conjugated (PEG) asparaginase alone (10-30 IU/kg intraperitoneally [IP] weekly--20 dogs) or PEG-asparaginase combined with one cycle of chemotherapy (vincristine, cyclophosphamide, methotrexate, and prednisone), followed by maintenance PEG-asparaginase (30 IU/kg, IP weekly--17 dogs). In the 20 dogs (eight were chemotherapy resistant) treated with PEG-asparaginase alone, seven had a complete response (CR), seven had a partial response (PR), five had no response (NR), and one was not evaluable (NE). The duration of response (CR + PR) ranged from 14 to 102 days (median, 48 days). In the eight chemotherapy-resistant dogs (seven were previously resistant to L-asparaginase) four had responses (one CR and three PR). In the 17 dogs treated with combined PEG-asparaginase and chemotherapy, 13 had a CR, two had a PR, and two had NR. None of the dogs had had prior chemotherapy, and the duration of response (CR + PR) ranged from 7 to 840+ days, with a median of 126+ days. Four dogs are still on maintenance PEG-asparaginase at 16+, 21+, 26+, and 28+ months. Toxicity consisted of death due to massive tumor breakdown (two dogs), disseminated intravascular coagulation (DIC--one dog), hypersensitivity reaction (one dog), vomiting (three dogs) and soft stools (three dogs). Four normal dogs were given very high doses of PEG-asparaginase (200 IU/kg and 1200 IU/kg) once weekly for two treatments without any significant toxicity. These results indicate that PEG-asparaginase has antitumor activity in dog with spontaneously occurring malignant lymphoma.
37只患有恶性淋巴瘤的犬只接受了以下治疗:单独使用聚乙二醇缀合(PEG)天冬酰胺酶(每周腹腔注射[IP]10 - 30 IU/kg,共20只犬),或PEG - 天冬酰胺酶联合一个化疗周期(长春新碱、环磷酰胺、甲氨蝶呤和泼尼松),随后进行维持性PEG - 天冬酰胺酶治疗(每周IP 30 IU/kg,共17只犬)。在单独接受PEG - 天冬酰胺酶治疗的20只犬(8只对化疗耐药)中,7只完全缓解(CR),7只部分缓解(PR),5只无反应(NR),1只无法评估(NE)。缓解持续时间(CR + PR)为14至102天(中位数为48天)。在8只化疗耐药犬(7只先前对L - 天冬酰胺酶耐药)中,4只出现反应(1只CR和3只PR)。在接受PEG - 天冬酰胺酶与化疗联合治疗的17只犬中,13只CR,2只PR,2只NR。所有犬均未接受过先前的化疗,缓解持续时间(CR + PR)为7至840 +天,中位数为126 +天。4只犬在16 +、21 +、26 +和28 +个月时仍在接受维持性PEG - 天冬酰胺酶治疗。毒性反应包括因大量肿瘤溶解导致的死亡(2只犬)、弥散性血管内凝血(DIC,1只犬)、过敏反应(1只犬)、呕吐(3只犬)和软便(3只犬)。4只正常犬每周一次接受非常高剂量的PEG - 天冬酰胺酶(200 IU/kg和1200 IU/kg),共两次治疗,未出现任何明显毒性。这些结果表明,PEG - 天冬酰胺酶对自发发生恶性淋巴瘤的犬具有抗肿瘤活性。