Vienna, Austria

ESTRO 2023

Session Item

Head and neck
6005
Poster (Digital)
Clinical
Health related QoL in patients with NPC treated with NACT followed by dysphagia-optimised CRT
Ahitagni Biswas, India
PO-1191

Abstract

Health related QoL in patients with NPC treated with NACT followed by dysphagia-optimised CRT
Authors:

Ahitagni Biswas1, Vivek Ghosh1, Swarnaditya Roy1, Suman Bhasker1, Ashish Binjola1, Madhavi Tripathi2, Aanchal Kakkar3, Raja Pramanik4, Atul Sharma4, Sampa Ghose4, Alok Thakar5, Krithika Rangarajan6, Chandrashekhara S.H.6, Chandrasekhar Bal2, Rajeev Malhotra7

1All India Institute of Medical Sciences, New Delhi, Radiation Oncology, New Delhi, India; 2All India Institute of Medical Sciences, New Delhi, Nuclear Medicine, New Delhi, India; 3All India Institute of Medical Sciences, New Delhi, Pathology, New Delhi, India; 4All India Institute of Medical Sciences, New Delhi, Medical Oncology, New Delhi, India; 5All India Institute of Medical Sciences, New Delhi, Otorhinolaryngology, New Delhi, India; 6All India Institute of Medical Sciences, New Delhi, Radiodiagnosis, New Delhi, India; 7All India Institute of Medical Sciences, New Delhi, Delhi Cancer Registry, New Delhi, India

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Purpose or Objective

We assessed the serial changes in health related quality of life(HR-QoL) parameters in patients with locally advanced nasopharyngeal carcinoma(LA-NPC) on a  phase 2 clinical trial of gemcitabine and cisplatin(GC) based neoadjuvant chemotherapy(NACT) followed by dysphagia optimised intensity modulated radiotherapy(Do-IMRT) with concurrent weekly cisplatin.

Material and Methods

Patients with stage II-IVA NPC received 3 cycles of 3-weekly NACT with cisplatin and gemcitabine followed by Do-IMRT(65Gy,60Gy,54Gy/30fractions/6weeks to high-risk, intermediate-risk and low-risk PTVs respectively by simultaneous integrated boost) with concurrent weekly cisplatin. Serial changes in HR-QoL were assessed by European Organisation for Research and Treatment of Cancer Quality of Life core-30 and Head and Neck Cancer Module(EORTC QLQ C-30 and H&N-35) questionnaire(version 3.0) at baseline, 3 weeks after completion of NACT, immediately and 3 and 6 months after completion of CRT. Serial changes in HR-QoL parameters at all time points were analysed by Friedman test and pair wise comparison was done by Wilcoxon signed rank test. Bonferroni correction for multiple comparisons was applied to control the type-I error.

Results

Out of a total of 30 screened patients, 23 were eligible and recruited in this study from 25-Sep-2020 to 01-Jan-2022. The CR rate and ORR after CRT were 78.6% and 92.9% respectively. The median duration of follow-up was 13.06 months. The actuarial PFS and OS rates were 100% and 90.3% at 1 year and 80.8% and 73.6% at 2 years, respectively. From a median global health status(GHS) score of 74.99 at baseline, there was an initial rise in the score after NACT(83.33), followed by a precipitous dip after CRT(33.33) and a subsequent steady rise in the scores at 3 months(58.33) and 6 months(83.33) after completion of CRT (p<0.001). Pertaining to physical, role, emotional, cognitive and social functioning, there was a dip in the median functional scale scores after NACT, which further intensified after completion of CRT, followed by a steady rise and partial recovery of the scores at 3 and 6 months after completion of CRT, the serial changes being all statistically significant. The median symptom scale scores for most of the domains of EORTC QLQ C-30 and H&N-35, particularly pain, swallowing, opening mouth, speech, dry mouth, sticky saliva and weight loss, peaked after CRT, followed by significant declines at 3 and 6 months after completion of CRT.

Conclusion

GC-based NACT followed by Do-IMRT with concomitant cisplatin was feasible and led to a favourable quality of life profile. There was an initial rise in the median GHS score after NACT, reflecting the high ORR of NACT followed by a precipitous dip after CRT due to the acute haematological and non-haematological toxicities of CRT. Subsequently there was a steady rise in the scores at 3 and 6 months after completion of CRT due to tumour response to CRT and resolution of acute toxicities.