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采用一体化加量的大分割调强放射治疗对乳腺癌进行为期四周的放射治疗。

Four-week course of radiation for breast cancer using hypofractionated intensity modulated radiation therapy with an incorporated boost.

作者信息

Freedman Gary M, Anderson Penny R, Goldstein Lori J, Ma Chang-Ming, Li Jinsheng, Swaby Ramona F, Litwin Samuel, Watkins-Bruner Deborah, Sigurdson Elin R, Morrow Monica

机构信息

Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.

出版信息

Int J Radiat Oncol Biol Phys. 2007 Jun 1;68(2):347-53. doi: 10.1016/j.ijrobp.2006.12.035. Epub 2007 Mar 26.

Abstract

PURPOSE

Standard radiation for early breast cancer requires daily treatment for 6 to 7 weeks. This is an inconvenience to many women, and for some a barrier for breast conservation. We present the acute toxicity of a 4-week course of hypofractionated radiation.

METHODS AND MATERIALS

A total of 75 patients completed radiation on a Phase II trial approved by the hospital institutional review board. Eligibility criteria were broad to include any patient normally eligible for standard radiation: age >or=18 years, invasive or in situ cancer, American Joint Committee on Cancer Stage 0 to II, breast-conserving surgery, and any systemic therapy not given concurrently. The median age was 52 years (range, 31-81 years). Of the patients, 15% had ductal carcinoma in situ, 67% T1, and 19% T2; 71% were N0, 17% N1, and 12% NX. Chemotherapy was given before radiation in 44%. Using photon intensity-modulated radiation therapy and incorporated electron beam boost, the whole breast received 45 Gy and the lumpectomy bed 56 Gy in 20 treatments over 4 weeks.

RESULTS

The maximum acute skin toxicity by the end of treatment was Grade 0 in 9 patients (12%), Grade 1 in 49 (65%) and Grade 2 in 17 (23%). There was no Grade 3 or higher skin toxicity. After radiation, all Grade 2 toxicity had resolved by 6 weeks. Hematologic toxicity was Grade 0 in most patients except for Grade 1 neutropenia in 2 patients, and Grade 1 anemia in 11 patients. There were no significant differences in baseline vs. 6-week posttreatment patient-reported or physician-reported cosmetic scores.

CONCLUSIONS

This 4-week course of postoperative radiation using intensity-modulated radiation therapy is feasible and is associated with acceptable acute skin toxicity and quality of life. Long-term follow-up data are needed. This radiation schedule may represent an alternative both to longer 6-week to 7-week standard whole-breast radiation and more radically shortened 1-week, partial-breast treatment schedules.

摘要

目的

早期乳腺癌的标准放疗需要每天进行治疗,持续6至7周。这给许多女性带来不便,对一些人来说也是保乳治疗的障碍。我们展示了4周超分割放疗疗程的急性毒性。

方法和材料

共有75名患者在一项经医院机构审查委员会批准的II期试验中完成了放疗。入选标准宽泛,包括任何通常符合标准放疗条件的患者:年龄≥18岁、浸润性或原位癌、美国癌症联合委员会分期0至II期、保乳手术以及未同时进行的任何全身治疗。中位年龄为52岁(范围31 - 81岁)。患者中,15%为导管原位癌,67%为T1期,19%为T2期;71%为N0,17%为N1,12%为NX。44%的患者在放疗前接受了化疗。采用光子调强放疗并结合电子束加量,全乳在4周内分20次接受45 Gy照射,局部切除床接受56 Gy照射。

结果

治疗结束时,最大急性皮肤毒性为0级的有9例患者(12%),1级的有49例(65%),2级的有17例(23%)。无3级或更高等级的皮肤毒性。放疗后,所有2级毒性在6周时均已消退。血液学毒性方面,大多数患者为0级,2例患者出现1级中性粒细胞减少,11例患者出现1级贫血。治疗后6周患者报告或医生报告的美容评分与基线相比无显著差异。

结论

这种采用调强放疗的4周术后放疗疗程是可行的,且急性皮肤毒性可接受,生活质量良好。需要长期随访数据。这种放疗方案可能是6至7周的标准全乳放疗以及更为激进的1周部分乳腺治疗方案的替代选择。

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