Hesdorffer Mary E, Chabot John A, Keohan Mary Louise, Fountain Karen, Talbot Susan, Gabay Michelle, Valentin Catherine, Lee Shing M, Taub Robert N
Division of Oncology, Columbia University New York, New York, USA.
Am J Clin Oncol. 2008 Feb;31(1):49-54. doi: 10.1097/COC.0b013e3180684181.
We report a single-institution Phase I or II trial of surgical debulking, intraperitoneal chemotherapy, and immunotherapy followed by whole abdominal radiotherapy in patients with malignant peritoneal mesothelioma.
Between 1997 and 2000, 27 patients with malignant peritoneal mesothelioma were enrolled: 23 with epithelial subtype and 4 with sarcomatoid or mixed subtype. The treatment regimen consisted of surgical debulking followed by 4 intraperitoneal courses of cisplatin alternating with 4 courses of doxorubicin, 4 doses of intraperitoneal gamma interferon, a second laparotomy with resection of residual disease plus intraoperative intraperitoneal mitomycin and cisplatin heated to 41 degrees C, and finally whole abdominal radiotherapy.
The median overall survival was 70 months with a 3-year survival of 67% (95% confidence interval, 46%-81%). Fourteen patients have died of their disease with a median time to death of 17 months (range, 0.4-71 months) after consenting to treatment. Seven patients are alive without evidence of disease with a median follow-up of 90 months (range, 71-110 months), and 6 are alive with disease with a median follow-up of 86 months (range, 70-106 months). The regimen was well tolerated. There were no patients with Grade III or IV hematological toxicities, 2 patients with Grade III ototoxicity, and 3 patients with Grade III gastrointestinal toxicity.
Based on the results of this study, intensive multimodality therapy appears feasible and effective in this group of patients.
我们报告了一项单机构的I期或II期试验,该试验针对恶性腹膜间皮瘤患者进行手术减瘤、腹腔内化疗和免疫治疗,随后进行全腹放疗。
1997年至2000年期间,纳入了27例恶性腹膜间皮瘤患者:23例为上皮亚型,4例为肉瘤样或混合亚型。治疗方案包括手术减瘤,随后进行4个疗程的顺铂腹腔内化疗与4个疗程的阿霉素交替使用,4剂腹腔内γ干扰素,第二次剖腹手术切除残留病灶并术中腹腔内注射丝裂霉素和顺铂并加热至41摄氏度,最后进行全腹放疗。
中位总生存期为70个月,3年生存率为67%(95%置信区间,46%-81%)。14例患者死于疾病,自同意治疗后至死亡的中位时间为17个月(范围,0.4-71个月)。7例患者存活且无疾病证据,中位随访时间为90个月(范围,71-110个月),6例患者存活但有疾病,中位随访时间为86个月(范围,70-106个月)。该方案耐受性良好。没有患者出现III级或IV级血液学毒性,2例患者出现III级耳毒性,3例患者出现III级胃肠道毒性。
基于本研究结果,强化多模式治疗在这组患者中似乎可行且有效。