Rogers L, Varia M, Halle J, Freddo J, Qaqish B, O'Keefe T, Fowler W
Department of Radiation Oncology, University of North Carolina, Chapel Hill 27599-7512.
Gynecol Oncol. 1993 Aug;50(2):141-6. doi: 10.1006/gyno.1993.1183.
Peritoneal seeding remains a prominent failure pattern in patients with invasive epithelial ovarian cancer, even following a pathologically negative second-look laparotomy (2LL). In an attempt to decrease the risk of peritoneal recurrence, we have treated patients with no clinical or histopathologic evidence of disease at 2LL with 15 mCi of chromic phosphate suspension intraperitoneally (32P).
Between 1973-1987, 69 patients with stages I-III invasive epithelial ovarian cancer in complete clinical remission were found to have no evidence of disease at 2LL. Fifty-one patients received intraperitoneal 32P. Thirty-five patients, otherwise eligible for 32P, did not receive it primarily due to other treatment protocols, peritoneal adhesions, or the recommendation that no further therapy be given following a negative 2LL. Patients in both groups were comparable with regard to stage, histology, grade, median age, residual disease following initial surgery, and chemotherapeutic regimen. The median follow-up for uncensored patients is 58 months (minimum, 18 months).
The 5-year actuarial disease-free survival rate from the date of 2LL was 86% for those receiving 32P and 67% for those not receiving 32P (P = 0.05). The corresponding 5-year overall survival rates were 90 and 78%, again favoring patients treated with 32P.
There were minimal acute side effects from 32P. Late adverse effects were similar in the two groups. Bowel complications were seen in 3 of 51 patients receiving 32P and 1 of 18 patients not receiving 32P.
We have found intraperitoneal 32P administration immediately after 2LL to be a safe and well-tolerated therapy. Our data suggest that 32P confers a survival advantage to patients with a pathologically negative 2LL. These findings suggest a continued role for second-look laparotomy with the use of 32P in selected patients.
即使在第二次剖腹探查术(2LL)病理检查结果为阴性之后,腹膜种植转移仍是侵袭性上皮性卵巢癌患者的一个主要失败模式。为了降低腹膜复发的风险,我们对在第二次剖腹探查术时无临床或组织病理学疾病证据的患者腹腔内注射15毫居里的磷酸铬悬浮液(32P)进行治疗。
1973年至1987年间,69例处于临床完全缓解期的I - III期侵袭性上皮性卵巢癌患者在第二次剖腹探查术时未发现疾病证据。51例患者接受了腹腔内32P注射。另外35例本符合32P治疗条件的患者未接受该治疗,主要原因是其他治疗方案、腹膜粘连或建议在第二次剖腹探查术阴性后不再进行进一步治疗。两组患者在分期、组织学、分级、中位年龄、初次手术后残留疾病以及化疗方案方面具有可比性。未删失患者的中位随访时间为58个月(最短18个月)。
从第二次剖腹探查术日期起计算,接受32P治疗患者的5年无病生存率为86%,未接受32P治疗患者为67%(P = 0.05)。相应的5年总生存率分别为90%和78%,同样表明接受32P治疗的患者更具优势。
32P的急性副作用极小。两组的晚期不良反应相似。接受32P治疗的51例患者中有3例出现肠道并发症,未接受32P治疗的18例患者中有1例出现肠道并发症。
我们发现第二次剖腹探查术后立即腹腔内注射32P是一种安全且耐受性良好的治疗方法。我们的数据表明,32P能为第二次剖腹探查术病理检查结果为阴性的患者带来生存优势。这些发现表明,在选定患者中,结合使用32P的第二次剖腹探查术仍可发挥作用。