Service d'Oncologie Médicale, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Département de radiodiagnostic, Institut Bergonié, Bordeaux, France.
Eur J Cancer. 2021 Jan;143:78-87. doi: 10.1016/j.ejca.2020.10.035. Epub 2020 Dec 5.
Desmoid tumours (DTs) are rare tumours originating from musculoaponeurotic structures. Although benign, they may be locally aggressive, leading to pain and disability. European Society for Medical Oncology (ESMO) guidelines recommend frontline watchful waiting and medical treatment in progressing tumours. Cryoablation is an interventional radiology technique that is suitable for DT patients (pts) on the basis of repeated cycles of freezing, leading to cell death.
CRYODESMO-01 (ClinicalTrials.gov Identifier: NCT02476305) is a prospective, open-label, non-randomised, non-comparative, multicenter study assessing cryoablation in non-abdominopelvic progressing DT. Inclusion criteria were: pts ≥18 y.o., confirmed DT accessible to cryoablation (≥90% destruction), measurable lesion conforming to modified response evaluation criteria in solid tumours (mRECIST), progressive disease after ≥2 lines of medical therapy or with functional symptoms/pain, adequate biological parameters, informed consent, and affiliation to a medical insurance scheme. The primary end-point was the non-progression rate at 12 months; secondary end-points included safety, quality of life (QoL), assessment of pain and functional status.
50 pts were enrolled (78% female) from four French centres and all were treated. The mean age was 41 y.o. (19-73). The median number of prior treatments was 2.00 [1-4] including non-steroidal anti-inflammatory drugs (NSAIDs), hormone therapy, chemotherapy, and anti-angiogenics. Tumour location included limbs (36%), trunk (60%), and cervical area (4%). The median tumour largest diameter was 89 mm. The rate of non-progressing disease at +12 months was 86% [confidence level (CI) 95% 73-94%]. Median PFS was not reached at a median follow-up of 31 months. Grade 1 and 2 toxicity occurred in 32.8% and 44.5% of patients, grade 3-4 in 22% and no Grade 5 toxicity was observed. Cryoablation significantly improved functional status and pain scores.
Cryoablation demonstrated feasibility in progressive DT pts. The study met is primary end-point with 86% of non-progressive disease at +12 months, with reduced pain, better functional status, and encouraging long-term disease control.
韧带样纤维瘤(DTs)是起源于肌肉腱膜结构的罕见肿瘤。尽管它们是良性的,但可能具有局部侵袭性,导致疼痛和残疾。欧洲肿瘤内科学会(ESMO)指南建议对进展中的肿瘤进行一线观察等待和药物治疗。冷冻消融是一种介入放射学技术,适用于基于多次冷冻循环的 DT 患者,导致细胞死亡。
CRYODESMO-01(ClinicalTrials.gov 标识符:NCT02476305)是一项前瞻性、开放标签、非随机、非对照、多中心研究,评估冷冻消融在非腹盆腔进展性 DT 中的应用。纳入标准为:年龄≥18 岁,可进行冷冻消融的确诊 DT(≥90%破坏),符合实体瘤改良反应评估标准(mRECIST)的可测量病变,在≥2 线药物治疗后进展或有功能症状/疼痛,有足够的生物学参数,知情同意,并参加医疗保险计划。主要终点为 12 个月时的无进展率;次要终点包括安全性、生活质量(QoL)、疼痛和功能状态评估。
来自法国的四个中心共纳入 50 名患者(78%为女性),均接受了治疗。平均年龄为 41 岁(19-73 岁)。中位数既往治疗次数为 2.00 [1-4],包括非甾体抗炎药(NSAIDs)、激素治疗、化疗和抗血管生成药物。肿瘤位置包括四肢(36%)、躯干(60%)和颈部(4%)。肿瘤最大直径中位数为 89 毫米。在+12 个月时,无进展疾病的比例为 86%[置信区间(CI)95% 73-94%]。中位无进展生存期(PFS)在中位随访 31 个月时未达到。32.8%和 44.5%的患者出现 1 级和 2 级毒性,22%的患者出现 3-4 级毒性,未观察到 5 级毒性。冷冻消融在进展性 DT 患者中表现出可行性。该研究达到了主要终点,在+12 个月时,无进展疾病的比例为 86%,疼痛减轻,功能状态改善,疾病长期控制效果令人鼓舞。