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Poster viewing 03

245P - Determine the effectiveness of PAlliative Split COurse RAdiotherapy (PASCORA) regimen in non-metastatic head and neck cancer patients who are treated with palliative intent: A retrospective single-centre study

Date

03 Dec 2022

Session

Poster viewing 03

Topics

Radiation Oncology;  Supportive and Palliative Care

Tumour Site

Head and Neck Cancers

Presenters

Umesh Velu

Citation

Annals of Oncology (2022) 33 (suppl_9): S1521-S1529. 10.1016/annonc/annonc1128

Authors

U. Velu1, P.S. Shetty2, K. SHARAN3, A. SINGH3, S. Lewis Salins3

Author affiliations

  • 1 Radiation Oncology Department, KMC - Kasturba Medical College, Manipal, 576104 - Manipal/IN
  • 2 Surgical Oncology, Kasturba Medical College and Hospital - Shirdi Sai Baba Cancer Center, 576104 - Manipal/IN
  • 3 Radiation Oncology Department, Kasturba Medical College and Hospital - Shirdi Sai Baba Cancer Center, 576104 - Manipal/IN

Resources

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Abstract 245P

Background

We at our centre practice a PAlliative Split COurse RAdiotherapy (PASCORA) of 22.5Gy in 5 fractions followed by a gap of 4 weeks and then again repeat 22.5Gy in 5 fractions for locally advanced squamous cell carcinoma patients treated with a palliative intent. Our primary aim is to determine the symptomatic relief at 3 months after completion of PASCORA regimen. Our secondary objective is to evaluate the overall survival (OS) in our patients.

Methods

49 Patients with histologically proven LAHNSCC between January 2014 to January 2021, planned for PASCORA regimen were evaluated. Retrospectively patient, tumor and treatment characteristics were retrieved. Symptomatic relief was assessed on a objective scale. OS was determined using Kaplan-Meir survival curves.

Results

Median age was 61 years, Multiple comorbidities (37%) were the most commonly documented reason for these patients being treated with a palliative intent. 25% of our patients had an excellent symptomatic relief, 26% of our patients had a good symptomatic relief and 31% had a partial relief. Median OS was 38 months in patients who had an excellent symptomatic relief and 3-8 months in patients with no or partial symptomatic relief (p value=0.000) 6% of our patients had grade 3 /4 RTOG toxicity.

Conclusions

PASCORA regimen offers a good symptomatic relief with good local control rates and acceptable level of toxicity and comparable OS. However, a larger prospective study with more patients and longer follow up would be required to confirm the same.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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