AI Article Synopsis

  • Patients with metastatic HPV-associated oropharyngeal cancer often have a good survival rate of over 2 years but face limited treatment options after immunotherapy, prompting the exploration of capecitabine as a salvage therapy.
  • A retrospective study investigated the outcomes of 10 patients who received capecitabine, primarily as a fourth-line treatment, with results showing a median survival of 10.5 months, and a clinical benefit rate of 70%.
  • Findings suggest that capecitabine may provide extended benefits for some heavily pretreated patients, but further research is needed to identify predictive factors for response and to confirm its efficacy through larger studies.

Article 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 ( = 8) and side effects ( = 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10715283PMC
http://dx.doi.org/10.6004/jadpro.2023.14.7.2DOI Listing

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