Capecitabine for Salvage Treatment of Patients With Heavily Pretreated Human Papillomavirus–Associated Oropharynx Cancer With Distant Metastases

Anna C. Cooper, PA-C, Casey A. Fazer, PA-C, Ashish V. Chintakuntlawar, MBBS, PhD, Harry E. Fuentes Bayne, MD, MS, Patrick W. McGarrah, MD, Katharine A. R. Price
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Abstract

Background: Patients with metastatic human papillomavirus–associated oropharyngeal cancer (HPV-OPC) have a median overall survival exceeding 2 years and are often candidates for multiple lines of palliative therapy. With the approval of immunotherapy as first-line treatment, salvage therapeutic options are limited. We describe our experience using capecitabine as salvage therapy for patients with recurrent or metastatic (R/M) HPV-OPC. Methods: We performed a retrospective study of patients with R/M HPV-OPC with distant metastatic disease. Eligible patients were identified from a medical oncology clinical database. Demographic and clinical data were abstracted from the medical record. Survival probabilities were estimated with the Kaplan-Meier method. Results: 10 patients were identified. Sites of metastatic disease included lung, liver, mediastinal lymph nodes, bone, abdominal lymph nodes, and soft tissue. Most patients received capecitabine as fourth-line treatment. The median duration from start of capecitabine therapy until death was 10.5 months. Best treatment response was as follows: partial responses (PR) were seen in 4 of 10 (40%), stable disease (SD) in 3 of 10 (30%), and progressive disease (PD) in 2 of 10 (20%). The clinical benefit rate (CR + PR + SD) was 70%. Reasons for discontinuation included disease progression (n = 8) and side effects (n = 2). One patient notably had prolonged benefit from capecitabine and continued to be on treatment for 34 months total. Conclusions: Capecitabine is a potential salvage treatment for heavily pretreated patients with R/M HPV-OPC, with some patients experiencing prolonged response. Clinical or molecular predictors of response would be helpful to identify patients likely to benefit; a larger prospective study would be useful to confirm efficacy in this patient population.
卡培他滨用于重度预处理人乳头状瘤病毒相关口咽癌远处转移患者的挽救治疗
背景:转移性人乳头瘤病毒相关口咽癌(HPV-OPC)患者的中位总生存期超过 2 年,通常需要接受多线姑息治疗。随着免疫疗法被批准作为一线治疗,挽救性治疗方案却很有限。我们介绍了将卡培他滨作为复发性或转移性(R/M)HPV-OPC 患者挽救疗法的经验。方法:我们对患有远处转移性疾病的 R/M HPV-OPC 患者进行了一项回顾性研究。符合条件的患者来自肿瘤内科临床数据库。人口统计学和临床数据摘自病历。采用 Kaplan-Meier 法估算生存概率。结果确定了 10 名患者。转移部位包括肺、肝、纵隔淋巴结、骨、腹腔淋巴结和软组织。大多数患者接受卡培他滨四线治疗。从开始接受卡培他滨治疗到死亡的中位时间为10.5个月。最佳治疗反应如下:10 例患者中有 4 例(40%)出现部分反应(PR),10 例患者中有 3 例(30%)病情稳定(SD),10 例患者中有 2 例(20%)病情进展(PD)。临床获益率(CR + PR + SD)为 70%。停药原因包括疾病进展(8 例)和副作用(2 例)。有一名患者明显延长了从卡培他滨治疗中获益的时间,并持续治疗了34个月。结论卡培他滨是R/M HPV-OPC重度预处理患者的一种潜在挽救治疗方法,部分患者可获得长期应答。临床或分子反应预测指标将有助于确定可能获益的患者;更大规模的前瞻性研究将有助于确认该患者群体的疗效。
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