Romano Edouard, Tran Sebastien, Ben Aissa Assma, Carvalho Goncalves Miguel, Durham André, Tsoutsou Pelagia
Department of Radiation Oncology, University Hospitals of Geneva, Geneva, Switzerland.
Department of Radiation Oncology, Vaud University Hospital Center, Lausanne, Switzerland.
Front Oncol. 2024 Oct 22;14:1449228. doi: 10.3389/fonc.2024.1449228. eCollection 2024.
Significant therapeutic changes have recently occurred in the management of melanoma brain metastases (BMs), both in the field of local treatments, with the rise of stereotactic radiotherapy (RT), as well as in systemic ones, with the advent of immunotherapy and targeted therapies (TT). These advances have brought about new challenges, particularly regarding the potential interactions between new TT (notably BRAF/MEK inhibitors) and irradiation. Through a clinical case, we will discuss a side effect not previously described in the literature: ultra-early pseudoprogression (PP) following brain stereotactic radiosurgery (SRS), in a patient treated with dabrafenib-trametinib.
A 61-year-old patient with BRAFV600E-mutated melanoma, receiving second-line dabrafenib-trametinib therapy, was referred for SRS on three progressing meningeal implants, without evidence of systemic progression. Four days after the first RT session (1x6 Gy on a fronto-orbital lesion prescribed 5x6 Gy, and 1x20 Gy single fraction on the other lesions), the patient presented with an epileptic seizure. An MRI, compared to the planning MRI ten days earlier, revealed significant progression of the irradiated lesions. The patient's condition improved with dexamethasone and levetiracetam, and RT was halted out of caution. A follow-up MRI at one month demonstrated a size reduction of all treated lesions. Subsequent imaging at five months revealed further shrinking of the two lesions treated with an ablative dose of 20 Gy, while the under-treated fronto-orbital lesion progressed. These dynamics suggest an initial PP in the three irradiated lesions, followed by good response in the ablatively treated lesions and progression in the partially treated lesion.
To our knowledge, this represents the first documented case of ultra-early PP following brain SRS in a patient receiving concomitant dabrafenib-trametinib. It highlights the need for particular vigilance when using tyrosine kinase inhibitors (TKIs) with SRS, and warrants further research into potential treatment interactions between RT and novel systemic agents, as well as the optimal treatment sequence of melanoma BMs.
近期,黑色素瘤脑转移(BMs)的治疗管理发生了重大变化,在局部治疗领域,立体定向放射治疗(RT)兴起;在全身治疗方面,免疫疗法和靶向治疗(TT)出现。这些进展带来了新的挑战,特别是新的TT(尤其是BRAF/MEK抑制剂)与放疗之间的潜在相互作用。通过一个临床病例,我们将讨论一种文献中此前未描述过的副作用:在接受达拉非尼-曲美替尼治疗的患者中,脑立体定向放射外科手术(SRS)后出现超早期假性进展(PP)。
一名61岁的BRAFV600E突变型黑色素瘤患者,正在接受二线达拉非尼-曲美替尼治疗,因三个进展性脑膜植入瘤被转诊接受SRS治疗,无全身进展证据。在第一次放疗疗程(对一个额眶部病灶给予1x6 Gy,处方剂量为5x6 Gy,对其他病灶给予1x20 Gy单次分割)后四天,患者出现癫痫发作。与十天前的计划MRI相比,MRI显示照射病灶显著进展。患者使用地塞米松和左乙拉西坦后病情改善,出于谨慎停止了放疗。一个月后的随访MRI显示所有治疗病灶尺寸缩小。五个月后的后续影像显示,接受20 Gy消融剂量治疗的两个病灶进一步缩小,而治疗不足的额眶部病灶进展。这些动态变化表明,三个照射病灶最初出现PP,随后接受消融治疗的病灶反应良好,而部分治疗的病灶进展。
据我们所知,这是接受达拉非尼-曲美替尼治疗的患者脑SRS后出现超早期PP的首例记录病例。它强调了在SRS联合使用酪氨酸激酶抑制剂(TKIs)时需要特别警惕,并值得进一步研究放疗与新型全身药物之间的潜在治疗相互作用,以及黑色素瘤BMs的最佳治疗顺序。