Williams C J, Mead B, Arnold A, Green J, Buchanan R, Whitehouse M
Cancer. 1982 May 1;49(9):1778-83. doi: 10.1002/1097-0142(19820501)49:9<1778::aid-cncr2820490908>3.0.co;2-z.
Thirty-five previously untreated patients with FIGO Stage III or IV ovarian carcinoma were treated with cis-diamminedichloroplatinum (II), Adriamycin and cyclophosphamide (PACe). Following four or five cycles of PACe, patients were assessed clinically for response. Twenty-one (60%) of the patients attained a clinical complete remission (CCR), seven (20%) a partial remission, and seven (20%) did not respond. The median survival of all patients was 19 months, 6.4 months for partial and nonresponders, and 26.5 months for clinical complete responders. Six patients remain relapse-free for more than two years. Patients entering into the study during the second year underwent a second-look procedure if they attained a CCR. Ten patients in CCR were assessed for second look; two refused, and eight underwent a laparotomy. Three of eight were in complete remission after second look, and a fourth patient who had microscopic disease in one ovary was rendered free of disease by surgery. Subjective toxicity was marked due to severe nausea and vomiting. Renal toxicity was not troublesome and myelosuppression was moderate. Ototoxicity and peripheral neuropathies were seen in seven patients. PACe is a highly effective induction regime but randomized studies are required to show that improved survival will result from it's use.
35例初治的国际妇产科联盟(FIGO)Ⅲ期或Ⅳ期卵巢癌患者接受顺二氨二氯铂(II)、阿霉素和环磷酰胺(PACe方案)治疗。在进行4或5个周期的PACe方案治疗后,对患者进行临床疗效评估。21例(60%)患者达到临床完全缓解(CCR),7例(20%)部分缓解,7例(20%)无反应。所有患者的中位生存期为19个月,部分缓解和无反应者为6.4个月,临床完全缓解者为26.5个月。6例患者无复发存活超过2年。在第二年进入该研究的患者若达到CCR则接受二次探查手术。对10例达到CCR的患者进行二次探查评估;2例拒绝,8例接受剖腹手术。8例中的3例在二次探查后完全缓解,第四例患者一侧卵巢有微小病灶,经手术清除病灶。由于严重恶心和呕吐,主观毒性明显。肾毒性不严重,骨髓抑制为中度。7例患者出现耳毒性和周围神经病变。PACe方案是一种高效的诱导方案,但需要进行随机研究以证明使用该方案可提高生存率。