Superficial radiotherapy and volumetric modulated Arc therapy for skin cancers within hamartomatous skin in patient with PTEN mutation: A case report

Nicole El-Turk, N. Holt, T. Gorjiara, G. Gottschalk, L. Krieger, L. Berglund, G. Fogarty
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Abstract

Phosphatase and tensin homolog (PTEN) gene acts as a tumour suppressor gene. Mutations of this gene are a step in the development of many cancers. Sufferers can have large fields of symptomatic hamartomatous skin change especially in sun exposed areas. RT has been reported to cause increased acute toxicity in this cohort. A 78-year-old fit male had a confirmed PTEN variant LRG_311t1 Exon 5, c353A>C. Symptomatic skin lesions of left frontal scalp and left nasal ala were confirmed on punch biopsy to be basal cell carcinoma (BCC) and he was referred for definitive radiotherapy (RT). He was treated with lesion based superficial radiotherapy to the left nasal ala to a total dose of 50 Gy in 25 fractions given at 5 fractions per week using a Xstrahl 300 machine via a 3cm circle applicator at 30cm source surface distance with a generating energy of 100 kV. The left frontal scalp was treated with a field-based volumetric modulated arc therapy technique to a planning target volume (PTV) of 74.8cm3 to 45 Gy with a simultaneous integrated boost PTV to 55 Gy of 4.1 cm3 to the BCC, all in 25 fractions. He developed the expected desquamation, erythema and mucositis within the nasal field and desquamation and erythema in the left temple. The PTEN mutation had no visible increase on the acute side effect profile compared with those without the mutation. After more than 6 months, the areas treated with RT remained clear of symptomatic hamartomatous skin change with no late toxicities. To our knowledge this is the longest benefit received of any treatment for fields of symptomatic hamartomatous skin change associated with PTEN mutation. It is also a report of not observing increased acute toxicity of RT in the definitive treatment of skin cancer in those with proven PTEN mutation. This one case adds evidence that definitive RT to skin may be delivered safely in this cohort. More studies with multiple patients with longer follow up are needed to confirm that those suffering with PTEN mutation can be safely and successfully treated with definitive RT for skin cancer and fields of symptomatic hamartomatous skin change with no increase in late effects.
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浅表放疗和体积调节电弧治疗错构瘤皮肤内PTEN突变患者的皮肤癌:1例报告
磷酸酶和紧张素同源基因(PTEN)是一种肿瘤抑制基因。这种基因的突变是许多癌症发展的一个步骤。患者可能会有大面积的症状性错构瘤皮肤变化,特别是在阳光照射的区域。据报道,RT在该队列中引起急性毒性增加。一名78岁男性确诊PTEN变异LRG_311t1外显子5,c353A>C。左额部头皮及左鼻翼有症状的皮肤病变,经穿刺活检证实为基底细胞癌(BCC),并转介行明确放疗(RT)。患者接受基于病变的左鼻翼浅表放射治疗,总剂量为50 Gy,分25次,每周5次,使用Xstrahl 300机器,通过3cm圆形涂抹器,在30cm源表面距离处进行放射治疗,产生能量为100 kV。采用基于场的体积调制弧线治疗技术治疗左额叶头皮至计划目标体积(PTV)为74.8cm3至45 Gy,同时对BCC进行综合PTV至55 Gy的4.1 cm3,全部分为25个分数。他出现了预期的鼻野脱皮、红斑和粘膜炎,左太阳穴脱皮和红斑。与没有突变的患者相比,PTEN突变在急性副作用方面没有明显增加。6个多月后,接受RT治疗的区域仍然没有症状性错构瘤性皮肤改变,没有晚期毒性。据我们所知,这是任何治疗与PTEN突变相关的症状性错构瘤性皮肤变化领域的最长获益。这也是一份报告,在证实PTEN突变的皮肤癌的最终治疗中,没有观察到RT的急性毒性增加。这一病例进一步证明,在这一队列中,皮肤放射治疗是安全的。需要对多例患者进行更多的研究,并进行更长时间的随访,以证实PTEN突变患者可以安全、成功地接受针对皮肤癌和症状性错构瘤性皮肤改变的最终RT治疗,而不会增加晚期效应。
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