Psycho-oncology/Supportive Care in Head–Neck Cancers Patients Undergoing Radiation Therapy: A Randomized Controlled Trial

Author:

Sinha Shwetabh1,Pandey Saket2,Salins Shirley L.3,Salins Naveen4ORCID,Deodhar Jayita5,Gupta Tejpal1,Laskar Sarbani G.1ORCID,Budrukkar Ashwini1,Swain Monali1,Kumar Anuj1,Murthy Vedang1,Nair Sudhir6,Nair Deepa6,Joshi Poonam6,Chaturvedi Pankaj6,Menon Nandini7ORCID,Patil Vijay7,Joshi Amit7,Noronha Vanita7ORCID,Prabhash Kumar7,Agarwal Jai Prakash1

Affiliation:

1. Department of Radiation Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, Maharashtra, India

2. Department of Radiation Oncology, Apollo Hospital, Lucknow, Uttar Pradesh, India

3. Department of Radiotherapy and Oncology, Kasturba Medical College, Manipal, Karnataka, India

4. Department of Palliative Medicine, Kasturba Medical College, Manipal, Karnataka, India

5. Department of Palliative Medicine, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, Maharashtra, India

6. Department of Head and Neck Surgery, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, Maharashtra, India

7. Department of Medical Oncology, Tata Memorial Centre, Homi Bhabha National Institute, Mumbai, Maharashtra, India

Abstract

An elevated level of distress is associated with poor health-related quality of life (QoL), decreased patient satisfaction, poor treatment compliance, and possible reduced survival. This randomized trial, conducted at a single center in India, enrolled head–neck cancer patients aged > 18 years who were undergoing curative intent radiation therapy, and had significant baseline distress as per the National Comprehensive Cancer Network distress thermometer (distress score ≥ 4). The patients were randomized into the Standard arm (STD), which involved routine assessment by the oncologist, or the Interventional arm (INV), where psycho-oncology/palliative/supportive care referral was done at baseline and every week during treatment. The study's primary endpoint was the proportion of patients having significant distress 6 months' posttreatment. A total of 212 patients were randomized (n = 108 STD, n = 104 INV). At 6 months' post-treatment completion, 90 and 89 were evaluable in the STD and INV, respectively. The median distress score was 2 in both arms at this time point. There was no significant difference in the proportion of patients having significant distress in STD versus INV (9 vs. 15.6%, p = 0.20). There was an improvement in any symptom measured by the Edmonton Symptom Assessment Score (pain, tiredness, drowsiness, nausea, lack of appetite) and the QoL for the entire cohort with no statistically significant difference between arms for symptoms, QoL, or survival endpoints. Psycho-oncology and palliative/supportive care referral did not impact distress, symptom burden, QoL, or survival at 6 months' posttreatment completion significantly in this randomized trial. Clinical Trial Registry of India Registration number: CTRI/2016/01/006549.

Publisher

Georg Thieme Verlag KG

Subject

Cancer Research,Oncology

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