Teshima T, Inoue T, Inoue T, Ikeda H, Sasaki S, Yamazaki H, Ohtani M, Murayama S, Kozuka T
Department of Radiology, Osaka University Medical School, Japan.
Radiat Med. 1993 Nov-Dec;11(6):237-41.
Our early experience using microSelectron HDR to treat cervical cancer patients at Osaka University Hospital is presented. From June 1991 through December 1992, a total of 20 patients (stage Ib, 6; stage IIa, 2; stage IIb, 5; stage IIIb, 6 and stage IVa, 1) with previously untreated invasive uterine cervical cancer and intact uterus were treated with high-dose rate intracavitary therapy administered with a microSelectron. For the treatment, a standard rigid applicator made of stainless steel for a microSelectron was used. Twenty to 30 Gy of external irradiation was administered to the whole pelvic field and 30 to 20 Gy to the central shielded field (total 50 Gy/5-6 weeks) for patients in stage II-IVa. For stage Ib, 40 Gy was delivered to the central shielded field. The 192Ir source had an activity of 370 GBq as of the measuring time. Source loading corresponded to the Manchester System for cervical cancer. Thirty-two or 30 Gy was administered at point A in four fractions over four weeks of intracavitary irradiation. Early primary tumor responses for all patients were complete. There have been two local recurrences in stage IIb and IIIb patients. Three patients in stages Ib, IIb, and IIIb developed para-aortic lymph node metastases, and two of them died from generalized metastasis. No acute radiation injury has been observed. One patient in stage IIb developed subileus five months after irradiation. From our early experience, it is concluded that microSelectron HDR can be used for cervical cancer patients as safely and effectively as our previously used high-dose rate machine.
本文介绍了我们在大阪大学医院使用微型Selectron高剂量率后装治疗机治疗宫颈癌患者的早期经验。从1991年6月至1992年12月,共有20例(Ib期6例;IIa期2例;IIb期5例;IIIb期6例;IVa期1例)未经治疗的浸润性子宫颈癌且子宫完整的患者接受了微型Selectron高剂量率腔内治疗。治疗时,使用了一种标准的微型Selectron不锈钢刚性施源器。对于II-IVa期患者,对整个盆腔野给予20至30 Gy的外照射,对中心屏蔽野给予30至20 Gy(总计50 Gy/5-6周)。对于Ib期患者,对中心屏蔽野给予40 Gy。截至测量时,192Ir源的活度为370 GBq。源加载符合宫颈癌的曼彻斯特系统。腔内照射在四周内分四次给予A点32或30 Gy。所有患者的早期原发肿瘤反应均为完全缓解。IIb期和IIIb期患者出现了两例局部复发。Ib期、IIb期和IIIb期的三名患者发生了腹主动脉旁淋巴结转移,其中两名患者死于全身转移。未观察到急性放射损伤。一名IIb期患者在照射后五个月出现了肠梗阻。根据我们的早期经验,得出结论:微型Selectron高剂量率后装治疗机可像我们之前使用的高剂量率机器一样安全有效地用于宫颈癌患者。