Govind Anjali, Rastogi Sameer, Pasricha Sunil, Ahmed Shamim, Goel Aastha
Department of Onco-Anesthesia and Palliative Medicine, All India Institute of Medical Sciences, New Delhi 110029, India.
Department of Medical Oncology, All India Institute of Medical Sciences, New Delhi 110029, India.
Ecancermedicalscience. 2025 May 15;19:1907. doi: 10.3332/ecancer.2025.1907. eCollection 2025.
With the advent of next-generation sequencing, increasingly we can sub classify the soft tissue sarcomas into various subtypes with distinct prognostic and therapeutic implications. Sarcomas with RAF1 mutations are extremely rare and so far, the treatment strategies are not known. Here, we report a case of a 48-year-old lady who initially presented with right ear swelling, which was excised and was suggestive of dermatofibrosarcoma protuberans with S100 expression. After a disease-free interval of 25 months, the patient relapsed with metastasis in the lung. Repeat biopsy and next-generation sequencing (NGS) were suggestive of PDZRN3/RAF1 fusion mutated sarcoma. On presentation, the patient had an Eastern Cooperative Oncology Group performance status of 4 and had respiratory distress due to lung metastasis. After consensus and decision in the molecular tumour board, the patient was started on low-dose trametinib and doxorubicin. After three cycles of treatment, the patient had a partial response and post six cycles she had a near-complete response. This case exemplifies the value of molecular characterisation of soft tissue sarcoma and adds to the already sparse literature for RAF1 mutated sarcomas.
随着下一代测序技术的出现,我们越来越能够将软组织肉瘤细分为具有不同预后和治疗意义的各种亚型。具有RAF1突变的肉瘤极为罕见,迄今为止,治疗策略尚不清楚。在此,我们报告一例48岁女性患者,最初表现为右耳肿胀,切除后提示为表达S100的隆突性皮肤纤维肉瘤。在无病间隔25个月后,患者复发并出现肺转移。再次活检和下一代测序(NGS)提示为PDZRN3/RAF1融合突变肉瘤。就诊时,患者东部肿瘤协作组(Eastern Cooperative Oncology Group)体能状态为4,因肺转移出现呼吸窘迫。在分子肿瘤委员会达成共识并做出决定后,患者开始接受低剂量曲美替尼和多柔比星治疗。三个周期的治疗后,患者出现部分缓解,六个周期后接近完全缓解。该病例例证了软组织肉瘤分子特征的价值,并为已有的关于RAF1突变肉瘤的稀少文献增添了内容。