Abstract

Background: Head and neck cancer (HNC) is one of the most common cancers in Pakistan. Disease free survival in HNC remains poor due to inefficient loco-regional disease control. The aim of the present study was to assess the response rate and toxicity of concomitant vinorelbine and External radiation therapy (ERT) in advanced Head and Neck cancer in local Pakistani population. The study as per Good Clinical Practice (GCP) guidelines was conducted at the oncology department of Nishat hospital Multan from 2015 to 2017. 
 Methodology: An observational, prospective study with enrollment of 50 patients of advanced head and neck cancer was followed to analyze the outcome for radiosensitization. Primary tumor sites were tongue in 15 (30%) patients; lower lip in 6 (12%); buccal cavity in 5 (10%); cheek in 5 (10%); tonsil in 4 (8%); larynx in 6 (12%); hypopharynx in 5 (10%); and parotid in 4 (8%) patients. Initial clinical stage was: IV in 23 (46%) patients and III in 27 (54%) patients. Vinorelbine (VNB) was given at dose of 10 mg i.v. infusion weekly with ERT (3D conformal radiation plan). Response rate was evaluated after at least 8 doses. Response evaluation criteria in Solid Tumors (RECIST) was used to assess complete response (CR) and partial response (PR); progressive disease (PD) and stable disease (SD). Toxicity was assessed using common toxicity criteria version 3.0 (CTCV3.0).
 Results: 44 out of 50 patients were evaluable for response rate and toxicity. Immediate response was 90% CR. After 24 months of followup CR, PR, SD, and PD were seen in 26 (59%), 6 (13%), 7 (15%) and 6 (13%) patients respectively. Grade III mucositis and dysphagia were observed in 19 (43%) and 8 (18%) patients respectively, grade III skin rash in 14 (30%) patients, grade-II peripheral neuropathy was seen in 3 (6%) patients.
 Conclusion: The study showed that vinorelbine as a radiosensitizer in advanced HNC is a feasible option with acceptable toxicities. A large study is required to define its definite role.

Highlights

  • Head and neck cancer (HNC) is one of the most common tobacco-related cancers worldwide[1], and squamous cell carcinoma is ninety percent (90%) of all HNC

  • A pilot study on vinorelbine as radiosensitizer in head & neck squamous cell carcinoma (HNSCC) & esophageal SCC has shown excellent results with less toxicity[16]. In this phase II study, we evaluated the response and toxicity of vinorelbine as a radiosensitizer in HNSCC

  • The current single centre study assesses the response rate and toxicity of concomitant vinorelbine and External radiation therapy (ERT) in advanced HNC in local Pakistani population. This was an observational, prospective, singlecentre study conducted at the department of radiotherapy and oncology, Nishtar hospital, a leading tertiary health care facility in Multan, Pakistan

Read more

Summary

Introduction

Head and neck cancer (HNC) is one of the most common tobacco-related cancers worldwide[1], and squamous cell carcinoma is ninety percent (90%) of all HNC. The long-term prognosis of patients with advanced HNC has been poor, because of metastatic disease, and primarily because of failure in locoregional disease control[2]. The primary treatment of head & neck squamous cell carcinoma (HNSCC) is surgery and radiotherapy. The use of multiagent chemoradiotherapy has been studied in patients with advanced HNSCC6. The aim of the present study was to assess the response rate and toxicity of concomitant vinorelbine and External radiation therapy (ERT) in advanced Head and Neck cancer in local Pakistani population. Methodology: An observational, prospective study with enrolment of 50 patients of advanced head and neck cancer was followed to analyze the outcome for radiosensitization. Results: 44 out of 50 patients were evaluable for response rate and toxicity. Conclusion: The study showed that vinorelbine as a radiosensitizer in advanced HNC is a feasible option with acceptable toxicities. A large study is required to define its definite role

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call