Creagan E T, Fleming T R, Edmonson J H, Ingle J N, Woods J E
Cancer. 1981 Jan 15;47(2):240-4. doi: 10.1002/1097-0142(19810115)47:2<240::aid-cncr2820470206>3.0.co;2-7.
Twenty-seven patients with measurable or evaluable, regionally advanced or metastatic head and neck cancer were given a combination of cyclophosphamide (C), Adriamycin (A), and cis-diamminedichloroplatinum (II) (P). Most patients had received extensive prior surgery and/or radiation therapy. Among 25 evaluable patients, the overall response rate was 64% (16/25) with 3/25 complete responders and 13/25 partial responders. The median survival for the entire group of 25 patients and the median response duration for the subset of 16 patients experiencing tumor regression were 8.1 and 7.0 months, respectively. Responders lived significantly longer than nonresponders (11 months vs. six months, P less than 0.01). According to covariate analysis, the difference seems to reflect the influence of response to treatment and not other confounding variables. Almost all patients experienced anorexia, nausea, vomiting, and a pervasive feeling of ill-health. In fact, six patients declined further treatment and five of these had objective tumor regressions. Recurrent disease was detected three months following discontinuation of chemotherapy in four of these five patients and seven months later in the fifth. Myelosuppression was clinically acceptable and there was in this dosage and schedule no evidence of hepatic or renal impairment. Although the CAP regimen has substantial antitumor activity, the program is clinically rigorous and should remain an investigational treatment modality at the present time.
27例患有可测量或可评估的局部晚期或转移性头颈癌的患者接受了环磷酰胺(C)、阿霉素(A)和顺二氨二氯铂(II)(P)的联合治疗。大多数患者此前已接受广泛的手术和/或放射治疗。在25例可评估的患者中,总缓解率为64%(16/25),其中3/25为完全缓解者,13/25为部分缓解者。25例患者的中位生存期以及16例肿瘤缩小患者亚组的中位缓解持续时间分别为8.1个月和7.0个月。缓解者的生存期明显长于未缓解者(11个月对6个月,P<0.01)。根据协变量分析,这种差异似乎反映了对治疗反应的影响,而非其他混杂变量。几乎所有患者都出现了厌食、恶心、呕吐以及普遍的健康不佳感。事实上,6例患者拒绝进一步治疗,其中5例有客观的肿瘤缩小。这5例患者中有4例在化疗停止3个月后检测到疾病复发,第5例在7个月后复发。骨髓抑制在临床上可以接受,按照这种剂量和方案,没有肝或肾功能损害的证据。尽管CAP方案有显著的抗肿瘤活性,但该方案临床要求严格,目前仍应作为一种试验性治疗方式。