Department of Radiation Oncology, Institut Curie, 26 rue d'Ulm, 75005 Paris, France.
Biomed Res Int. 2013;2013:264306. doi: 10.1155/2013/264306. Epub 2013 Sep 2.
We investigated the feasibility of helical tomotherapy (HT) for inoperable large breast tumors, after failing to achieve adequate treatment planning with conformal radiation techniques.
Five consecutive patients with locally advanced breast cancer (LABC) were treated by preoperative HT. All patients received up-front chemotherapy before HT. Irradiated volumes included breast and nodal areas (45-50 Gy) in 4 patients. One patient received a simultaneous integrated boost (55 Gy) to gross tumor volume (GTV) without lymph node irradiation. Acute toxicity was assessed with Common Toxicity Criteria for Adverse Events v.4. Patients were evaluated for surgery at the end of treatment.
Patients were staged IIB to IIIC (according to the AJCC staging system 2010). HT was associated in 4 patients with concomitant chemotherapy (5-fluorouracil and vinorelbine). Two patients were scored with grade 3 skin toxicity (had not completed HT) and one with grade 3 febrile neutropenia. One patient stopped HT with grade 2 skin toxicity. All patients were able to undergo mastectomy at a median interval of 43 days (31-52) from HT. Pathological partial response was seen in all patients.
HT is feasible with acceptable toxicity profiles, potentially increased by chemotherapy. These preliminary results prompt us to consider a phase II study.
我们研究了在常规放疗技术无法达到充分治疗计划的情况下,使用螺旋断层放疗(HT)治疗不可手术的大型乳腺肿瘤的可行性。
5 例局部晚期乳腺癌(LABC)患者接受术前 HT 治疗。所有患者在 HT 前均接受了先期化疗。4 例患者的照射区域包括乳房和淋巴结区域(45-50Gy)。1 例患者未行淋巴结照射,对大体肿瘤体积(GTV)行同步整合增敏放疗(55Gy)。采用不良事件通用毒性标准 v.4 评估急性毒性。治疗结束时,对患者进行手术评估。
患者分期为 IIB 至 IIIC(根据 AJCC 分期系统 2010 年)。HT 联合化疗(氟尿嘧啶和长春瑞滨)在 4 例患者中进行。2 例患者出现 3 级皮肤毒性(未完成 HT),1 例出现 3 级发热性中性粒细胞减少症。1 例患者因 2 级皮肤毒性停止 HT。所有患者均能在 HT 后中位 43 天(31-52 天)内行乳房切除术。所有患者均可见病理性部分缓解。
HT 具有可接受的毒性特征,可能因化疗而增加。这些初步结果促使我们考虑开展 II 期研究。