Freedman Gary M, Li Tianyu, Nicolaou Nicos, Chen Yan, Ma Charlie C-M, Anderson Penny R
Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Int J Radiat Oncol Biol Phys. 2009 Jul 1;74(3):689-94. doi: 10.1016/j.ijrobp.2008.08.071. Epub 2009 Apr 11.
To study the time spent with radiation-induced dermatitis during a course of radiation therapy for breast cancer in women treated with conventional or intensity-modulated radiation therapy (IMRT).
The study population consisted of 804 consecutive women with early-stage breast cancer treated with breast-conserving surgery and radiation from 2001 to 2006. All patients were treated with whole-breast radiation followed by a boost to the tumor bed. Whole-breast radiation consisted of conventional wedged photon tangents (n = 405) earlier in the study period and mostly of photon IMRT (n = 399) in later years. All patients had acute dermatitis graded each week of treatment.
The breakdown of the cases of maximum acute dermatitis by grade was as follows: 3%, Grade 0; 34%, Grade 1; 61%, Grade 2; and 2%, Grade 3. The breakdown of cases of maximum toxicity by technique was as follows: 48%, Grade 0/1, and 52%, Grade 2/3, for IMRT; and 25%, Grade 0/1, and 75%, Grade 2/3, for conventional radiation therapy (p < 0.0001). The IMRT patients spent 82% of weeks during treatment with Grade 0/1 dermatitis and 18% with Grade 2/3 dermatitis, compared with 29% and 71% of patients, respectively, treated with conventional radiation (p < 0.0001). Furthermore, the time spent with Grade 2/3 toxicity was decreased in IMRT patients with small (p = 0.0015), medium (p < 0.0001), and large (p < 0.0001) breasts.
Breast IMRT is associated with a significant decrease both in the time spent during treatment with Grade 2/3 dermatitis and in the maximum severity of dermatitis compared with that associated with conventional radiation, regardless of breast size.
研究接受传统放疗或调强放疗(IMRT)的女性乳腺癌患者在放疗过程中出现放射性皮炎的时间。
研究对象为2001年至2006年期间连续804例接受保乳手术及放疗的早期乳腺癌女性患者。所有患者均接受全乳放疗,随后对瘤床进行加量照射。在研究前期,全乳放疗采用传统楔形光子切线野(n = 405),后期则大多采用光子IMRT(n = 399)。所有患者在治疗的每周均对急性皮炎进行分级。
按级别划分的最大急性皮炎病例分布如下:0级占3%;1级占34%;2级占61%;3级占2%。按技术划分的最大毒性病例分布如下:IMRT中,0/1级占48%,2/3级占52%;传统放疗中,0/1级占25%,2/3级占75%(p < 0.0001)。IMRT患者在治疗期间0/1级皮炎的周数占82%,2/3级皮炎的周数占18%,而接受传统放疗的患者分别为29%和71%(p < 0.0001)。此外,乳房小(p = 0.0015)、中(p < 0.0001)、大(p < 0.0001)的IMRT患者出现2/3级毒性的时间均减少。
与传统放疗相比,无论乳房大小,乳腺IMRT均与2/3级皮炎治疗期间的时间显著减少以及皮炎的最大严重程度显著降低相关。