Partial response to erlotinib in a patient with imatinib-refractory sacral chordoma.

Saurav Verma, Surya Prakash Vadlamani, Shamim Ahmed Shamim, Adarsh Barwad, Sameer Rastogi, S T Arun Raj
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引用次数: 4

Abstract

Background: Chordoma is a rare, slow growing and locally aggressive mesenchymal neoplasm with uncommon distant metastases. It is a chemo-resistant disease with surgery and radiotherapy being the mainstay in treatment of localized disease. In advanced disease imatinib has a role. We report a case of metastatic sacral chordoma with symptomatic and radiological response to erlotinib post-progression on imatinib.

Case presentation: A 48-year-old male with a sacral chordoma underwent partial sacrectomy followed by post-operative radiotherapy. Upon recurrence he received palliative radiotherapy to hemipelvis and was offered therapy with imatinib. However, the disease was refractory to imatinib and he was started on treatment with erlotinib-showing a partial response on imaging at two months. He is currently doing well at 13 months since start of erlotinib.

Conclusions: As seen in previously reported cases, erlotinib is a therapeutic option in advanced chordoma, even in imatinib refractory cases and thus warrants exploration of its therapeutic role in prospective clinical trials.

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伊马替尼难治性骶脊索瘤患者对厄洛替尼的部分缓解。
背景:脊索瘤是一种罕见、生长缓慢、局部侵袭性的间充质肿瘤,常发生远处转移。它是一种耐化疗的疾病,手术和放疗是治疗局限性疾病的主要方法。在晚期疾病中,伊马替尼发挥作用。我们报告一例转移性骶脊索瘤,在伊马替尼进展后对厄洛替尼有症状和放射反应。病例介绍:一例48岁男性骶骨脊索瘤行部分骶骨切除术,术后行放射治疗。复发后接受半骨盆姑息性放疗,并给予伊马替尼治疗。然而,该疾病对伊马替尼难治性,他开始用厄洛替尼治疗,两个月时影像学显示部分缓解。目前,他在开始使用厄洛替尼13个月后恢复良好。结论:正如先前报道的病例所见,厄洛替尼是晚期脊索瘤的一种治疗选择,即使在伊马替尼难治性病例中也是如此,因此值得在前瞻性临床试验中探索其治疗作用。
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期刊介绍: Clinical Sarcoma Research considers for publication articles related to research on sarcomas, including both soft tissue and bone. The journal publishes original articles and review articles on the diagnosis and treatment of sarcomas along with new insights in sarcoma research, which may be of immediate or future interest for diagnosis and treatment. The journal also considers negative results, especially those from studies on new agents, as it is vital for the medical community to learn whether new agents have been proven effective or ineffective within subtypes of sarcomas. The journal also aims to offer a forum for active discussion on topics of major interest for the sarcoma community, which may be related to both research results and methodological topics.
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