Cervenakov I, Szoldova K, Mardiak J, Chovan D, Mala M, Slavov D
Department of Urology and Andrology, University Hospital, Bratislava, Slovakia.
Bratisl Lek Listy. 2000;101(6):317-20.
To ascertain the effect of intravesical instillation of Alpha 2-b Interferon (IFN a-2) 10 million I.U. in 50 ml physiological saline as a monotherapy and in combination with Farmarubicin (FRC) 50 mg dissolved together in 50 ml of physiological saline. These substances were administered four times during the first month after TUR-BT and then once monthly for one year either in the form of an IFN a-2 monotherapy or as an IFN a-2 and FRC combination in the therapy of recurrence of transitional cell carcinoma (TCC) of the urinary bladder after transurethral resection of the bladder tumor (TUR-BT). THEORETICAL CONSIDERATION: One of the causes of malignancy is an irreversible shift in the balance between protooncogens and tumor supressorgens. In the genetical process of the control of cell apoptosis, an important role is played by the tumor-supressorgen p 53. By the means of mutation of protooncogenes, cellular oncogenes(C-MYC) are formed, inducing the proliferation of cells of the tumor and via feedback induce also the p53 mutation. By the reduction of cellular oncogenes, IFN a-2 and FRC intervene by blocking the proliferation of tumor cells.
Authors have checked and treated 33 patients (pts) with recurrent TCC. The first group of 20 pts were after TUR-BT with BCG unsuccessful intravesical therapy, and 13 pts in the second group were with recurrence of TCC, but contraindicated for BCG treatment. These 33 pts (the first and second groups) were compared with 33 pts of the third group after TUR-BT but without intravesical instillation therapy. The pts of the third group did not suffer from any other significant ailment. IFN a-2 monotherapy (10 mill. I.U./or a combination of IFN a-2 + FRC (50 mg/50 ml solution were administered for 2 hours, 1 week after TUR-BT. During the first month, instillations were done weekly, from the second to the twelfth month only once monthly. The results were evaluated for 12 to 33 months (median: 24 months).
Group I: From 20 pts after TUR-BT + unsuccessful BCG + IFN a-2 monotherapy recurrence was registered in 4 pts (20%). Group II: Out of 13 pts after TUR-BT + IFN a-2 + FRC, recurrence was registered in 3 pts (23%). Group I + II: Recurrence in both groups was observed in 7 pts (21.2%). Group III: Out of 33 pts after TUR-BT without immuno- et chemotherapy recurrence was registered in 18 pts (54.5%). After one year of treatment, patients were checked for 24 months. The transition into an invasive tumor was observed in 4 pts (12.1%). In the comparative group of 33 pts without instillation after TUR-BT, recurrence was detected after one year in 18 pts (54.5%) and the transition into an invasive tumor was observed in 7 pts (21.2%).
Intravesical instillation of BCG used to be the most frequently applied therapy following TUR-BT. The toxicity of this vaccine as well as the contraindication of this treatment in some diseases, and also the primary or secondary resistance of TCC to BCG have challenged the search for alternative possibilities of the intravesical instillation treatment. IFN a-2 monotherapy and IFN a-2 in combination with FRC are new alternative approaches in the improvement of TCC treatment. This therapy is also supported by research of molecular genetics. (Ref.18.)
确定膀胱内灌注1000万国际单位α2 - b干扰素(IFNα - 2)溶于50毫升生理盐水中作为单一疗法,以及与50毫克表柔比星(FRC)一起溶于50毫升生理盐水中联合使用的效果。这些物质在经尿道膀胱肿瘤电切术(TUR - BT)后的第一个月内给药4次,然后每月给药1次,持续一年,采用IFNα - 2单一疗法或IFNα - 2与FRC联合疗法治疗膀胱移行细胞癌(TCC)经尿道膀胱肿瘤电切术后的复发。理论考量:恶性肿瘤的原因之一是原癌基因和肿瘤抑制基因之间平衡的不可逆转变。在细胞凋亡控制的遗传过程中,肿瘤抑制基因p53起重要作用。通过原癌基因突变形成细胞癌基因(C - MYC),诱导肿瘤细胞增殖,并通过反馈也诱导p53突变。通过减少细胞癌基因,IFNα - 2和FRC通过阻断肿瘤细胞增殖发挥作用。
作者检查并治疗了33例复发性TCC患者。第一组20例患者为TUR - BT后膀胱内卡介苗(BCG)治疗失败,第二组13例患者为TCC复发,但禁忌BCG治疗。将这33例患者(第一组和第二组)与第三组33例TUR - BT后未进行膀胱内灌注治疗的患者进行比较。第三组患者无任何其他重大疾病。IFNα - 2单一疗法(1000万国际单位)或IFNα - 2 + FRC联合疗法(50毫克/50毫升溶液)在TUR - BT后1周给药2小时。在第一个月内每周进行灌注,从第二个月到第十二个月每月仅进行一次灌注。结果评估12至33个月(中位数:24个月)。
第一组:20例TUR - BT + BCG治疗失败 + IFNα - 2单一疗法的患者中,4例(20%)出现复发。第二组:13例TUR - BT + IFNα - 2 + FRC的患者中,3例(23%)出现复发。第一组 + 第二组:两组中均有7例(21.2%)出现复发。第三组:33例TUR - BT后未进行免疫及化疗的患者中,18例(54.5%)出现复发。治疗一年后,对患者进行24个月的检查。4例(12.1%)观察到向浸润性肿瘤转变。在33例TUR - BT后未进行灌注的对照组中,一年后18例(54.5%)检测到复发,7例(21.2%)观察到向浸润性肿瘤转变。
膀胱内灌注BCG过去是TUR - BT后最常用的治疗方法。这种疫苗的毒性以及该治疗在某些疾病中的禁忌证,以及TCC对BCG的原发性或继发性耐药性,促使人们寻找膀胱内灌注治疗的替代方法。IFNα - 2单一疗法和IFNα - 2与FRC联合疗法是改善TCC治疗的新替代方法。该疗法也得到了分子遗传学研究的支持。(参考文献18)