马绍康, 高菊珍, 吴令英, 王亚菲, 张宏志, 黄曼妮. 宫颈癌复发肿瘤适形照射联合化疗30例临床观察[J]. 中国肿瘤临床, 2006, 33(2): 96-98.
引用本文: 马绍康, 高菊珍, 吴令英, 王亚菲, 张宏志, 黄曼妮. 宫颈癌复发肿瘤适形照射联合化疗30例临床观察[J]. 中国肿瘤临床, 2006, 33(2): 96-98.
Ma Shaokang, Gao Juzhen, Wu Lingying, Wang Yafei, Zhang Hongzhi, Huang Manni. Three-dimensional Conformal Radiotherapy with Concurrent Chemotherapy for Recurrent Carcinoma of the Cervix: An Analysis of 30 Cases[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2006, 33(2): 96-98.
Citation: Ma Shaokang, Gao Juzhen, Wu Lingying, Wang Yafei, Zhang Hongzhi, Huang Manni. Three-dimensional Conformal Radiotherapy with Concurrent Chemotherapy for Recurrent Carcinoma of the Cervix: An Analysis of 30 Cases[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2006, 33(2): 96-98.

宫颈癌复发肿瘤适形照射联合化疗30例临床观察

Three-dimensional Conformal Radiotherapy with Concurrent Chemotherapy for Recurrent Carcinoma of the Cervix: An Analysis of 30 Cases

  • 摘要: 目的:研究三维适形照射技术(ThreeDimensionalConformalRadiationTherapy,3DCRT)联合化疗治疗宫颈癌复发肿瘤病灶,探讨其临床效果。方法:针对宫颈癌放疗后复发病灶的照射。13例放疗后复发,原照射野内复发者,适形照射剂量DT20~40Gy,照射野外复发者(主动脉旁淋巴结)适形照射DT60~70Gy;17例宫颈癌根治术后盆腔复发患者,全盆腔常规照射DT40~45Gy,针对病灶适形照射DT25~30Gy;腹主动脉旁淋巴结转移者,适行照射DT60~70Gy。放疗过程中联合化疗,方案为:5-FU4g/96h静脉点滴,PDD30mgD1~4静脉冲入。结果:随访时间为6~40个月。1)86.6%26/30例有疼痛症状,76.9%(20/26)完全缓解,23.1%(6/26)部分缓解,有效率为100%。2)30例患者,CR16例,PR11例,SD3例,有效率90%。肿瘤缓解时间:3~40个月,中位5个月,平均12.3个月;有12例肿瘤再次进展。3)28例行SCC检查,治疗前25例高于1.5ng/ml者,治疗后23例(82.2%)降到正常,5例下降但未至正常,17.8%。4)生存超过1年者11例(36.7%);超过2年者4例(13.3%);超过3年者2例(6.7%)。5)近期并发症,骨髓抑制≤Ⅲ度者11例(36.7%),Ⅳ度者2例(6.7%);消化道症状2例(6.7%)。2,远期并发症,放射性膀胱炎1例(3.3%)。结论:适形照射联合化疗近期效果好,特别是腹主动脉旁淋巴结转移灶的患者;而放射治疗野内的复发病灶,因受剂量的限制,治疗效果不佳。

     

    Abstract: Objective: To evaluate the three-dimensional conformal radiation therapy (3DCRT) with concurrent chemotherapy for recurrent carcinoma of the cervix. Methods: A total of 30 patients were divided into 2 groups: 13 patients with failure after radiotherapy, doses of 3DCRT for relapse at pelvis were 20 to 40Gy and 60 to 70Gy for distant failure (para-aortic lymph nodes); 17 patients with failure after radical surgery, conventionally radiated 40 to 45Gy for pelvis and 3DCRT 25 to 30Gy for tumor site in patients with pelvic relapse, 3DCRT 60~70Gy for patients with para-aortic metastases. Concurrent chemotherapy with cisplatin 30mg D1 to D4 and 5-fluorouracil 4g/96h. Results: 1) In 26 of the 30 patients (86.6%) suffering from pain, there were 20 complete pain relief responses (76.9%) and 6 partial responses (23.1%), for an overall response rate of 100%. In 13 patients suffering from sciatic pain and leg edema, there were 8 patients with CR (61.5%) and 5 patients with PR (38.5%). 2) Tumor regression: In all 30 patients, there were 16 CRs (53.3%), 11 PRs (36.7%) and 3 SDs (10%) and the overall response rate was 90%. Response duration: Median duration was 5 months and mean duration was 12.3 months with range 3 to 40 months. There were 12 patients with tumor progression after response to treatment. 3) Tumor marker SCC: In 28 patients having serum SCC measurement, there were 25 patients with SCC level > 1.5ng/ml (2.2-67.4ng/ml). Of the 25 patients, 23 patients' SCC decreased to normal level (82.2%) and 5 patients decresed but not to normal level (17.8%). 4) Survival: Up to date, 11 patients survived more than 1 year (36.7%), and 4 patients more than 2 years (13.3%) and 2 patients more than 3 years (6.7%). Complications: Less than grade III haematologic toxicity occurred in 36.7% (11 patients) and grade IV 6.7% (2 patients). There was a 6.7% gastrointestinal toxicities (2 patients) in the cases and 1 patient (3.3%) developed to grade II late bladder toxicity (chronic bleeding). Conclusion: 3DCRT and concurrent chemotherapy for recurrent carcinoma of the cervix are effective to a 100% subjective response and 90% tumor response. The complication does not increase while escalating the radiation dose. 3DCRT for isolated para-aortic lymph nodes metastases gets a superior effect to other site relapse. Patients with recurrence after definitive radiotherapy located within pelvis have no CR and the prognosis is not good.

     

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