Nashiro Tsuguhisa, Yagi Chiaki, Hirakawa Makoto, Inamine Morihiko, Nagai Yutaka, Sakumoto Kaoru, Tamaki Wakana, Ogawa Kazuhiko, Toita Takafumi, Aoki Yoichi
Department of Obstetrics and Gynecology, Faculty of Medicine, University of the Ryukyus, 207 Uehara Nishihara, Okinawa, Japan.
Int J Clin Oncol. 2008 Aug;13(4):335-9. doi: 10.1007/s10147-007-0758-7. Epub 2008 Aug 15.
We reviewed our experience with patients with primary squamous cell carcinoma of the vagina who received concurrent chemoradiation therapy (CCRT).
We retrospectively analyzed six patients (median age, 60 years) with squamous cell carcinoma of the vagina who underwent CCRT between 2002 and 2005 at the University of the Ryukyus Hospital. Two patients were in International Federation of Obstetricians and Gynecologists (FIGO) stage II, one in stage III, and three in stage IVA. All patients had an Eastern Cooperative Oncology Group (ECOG) performance status of 2 or less. Tumor size ranged from 3.2 to 7.7 cm. All patients were treated with true pelvic external-beam radiotherapy (EBRT) at 50 Gy. Then two of the six patients underwent intracavitary vaginal brachy-therapy. The remaining four patients received boost EBRT with shrinking fields. Total radiation dose to the vaginal tumor ranged from 60 to 66 Gy. All patients received two or three concomitant cycles of cisplatin during EBRT.
All six patients completed their scheduled CCRT, and achieved a clinical complete response. One stage II patient died of disease 24 months after treatment, and the stage III patient had local failure at 12 months. The remaining four patients were free of their disease at 18, 23, 33, and 55 months, respectively. One patient with stage IVA developed a vesicovaginal fistula during CCRT. Nevertheless, CCRT was well tolerated by all six patients, and no grade 3 or 4 late toxicity was observed, as evaluated by the Radiation Therapy Oncology Group (RTOG) scoring system.
CCRT is effective for primary squamous cell carcinoma of the vagina and should be considered for treatment in patients with high-risk disease having good performance status.
我们回顾了原发性阴道鳞状细胞癌患者接受同步放化疗(CCRT)的经验。
我们回顾性分析了2002年至2005年间在琉球大学医院接受CCRT的6例阴道鳞状细胞癌患者(中位年龄60岁)。2例为国际妇产科联盟(FIGO)II期,1例为III期,3例为IVA期。所有患者东部肿瘤协作组(ECOG)体能状态均为2分或更低。肿瘤大小为3.2至7.7厘米。所有患者均接受50 Gy的真骨盆外照射放疗(EBRT)。然后6例患者中有2例接受了腔内阴道近距离放疗。其余4例患者接受缩野加量EBRT。阴道肿瘤的总辐射剂量为60至66 Gy。所有患者在EBRT期间接受了两或三个顺铂同步周期治疗。
所有6例患者均完成了预定的CCRT,并实现了临床完全缓解。1例II期患者在治疗后24个月死于疾病,III期患者在12个月时出现局部复发。其余4例患者分别在18、23、33和55个月时无疾病复发。1例IVA期患者在CCRT期间发生膀胱阴道瘘。然而,所有6例患者对CCRT耐受性良好,根据放射肿瘤学组(RTOG)评分系统评估,未观察到3级或4级晚期毒性反应。
CCRT对原发性阴道鳞状细胞癌有效,对于体能状态良好的高危疾病患者应考虑采用该治疗方法。