Dong M, Li X, Hong L-J, Xie R, Zhao H-L, Li K, Wang H-H, Shin W-D, Shen H-J
Department of Medical Oncology, Fourth Affiliated Hospital of Harbin Medical University, Harbin, China.
J Int Med Res. 2008 Nov-Dec;36(6):1273-8. doi: 10.1177/147323000803600614.
The aim of this study was to evaluate the efficacy of recombinant adenovirus p53 agent (rAd-p53) injection combined with cisplatin (CDDP) for the treatment of malignant pleural or peritoneal effusion. After puncture drainage, patients in the treatment group (n = 27) received intracavitary administration of rAd-p53 (2 x 10(12) virus particles) once a week for 4 weeks. At 48 h after each rAd-p53 injection, patients were given intracavitary administration of cisplatin 60 mg/m(2). This administration procedure continued once a week for 4 weeks. The control group (n = 21) received the same intracavitary therapy as the treatment group but without rAd-p53 therapy. Efficacy was evaluated by clinical observations, computed tomography, tumour markers, Karnofsky score and short-term follow-up. The total effective rates for the treatment group (63.0%) were significantly higher than for the control group (42.9%), suggesting that the treatment group benefited over the control group. In conclusion, rAd-p53 therapy is a safe and effective treatment for advanced malignant pleural or peritoneal effusion.
本研究旨在评估重组腺病毒p53制剂(rAd-p53)联合顺铂(CDDP)治疗恶性胸腔或腹腔积液的疗效。穿刺引流后,治疗组(n = 27)患者每周接受1次rAd-p53腔内注射(2×10¹²病毒颗粒),共4周。每次rAd-p53注射后48小时,患者接受顺铂60 mg/m²腔内注射。此给药程序每周进行1次,共4周。对照组(n = 21)接受与治疗组相同的腔内治疗,但不进行rAd-p53治疗。通过临床观察、计算机断层扫描、肿瘤标志物、卡诺夫斯基评分和短期随访评估疗效。治疗组的总有效率(63.0%)显著高于对照组(42.9%),表明治疗组比对照组更具优势。总之,rAd-p53治疗是晚期恶性胸腔或腹腔积液的一种安全有效的治疗方法。