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E-Poster Display

959P - Analysis of concurrent chemo-radiation using weekly cisplatin in locally advanced SCCHN: Identification of prognostic factors

Date

17 Sep 2020

Session

E-Poster Display

Topics

Cytotoxic Therapy

Tumour Site

Head and Neck Cancers

Presenters

Atul Sharma

Citation

Annals of Oncology (2020) 31 (suppl_4): S599-S628. 10.1016/annonc/annonc277

Authors

A. Sharma1, B.K. Mohanti2, A. Thakar3, S. Bhasker4, K. Sikka3, A.C. Singh3, R. Pramanik1, R. Kumar3, A. Biswas4, S. Deo5, S. Thulkar6, S. Bahadur7

Author affiliations

  • 1 Medical Oncology Department, AIIMS - All India Institute of Medical Sciences, 110029 - New Delhi/IN
  • 2 Radiation Oncology Department, Formerly at AIIMS - All India Institute of Medical Sciences, 110029 - New Delhi/IN
  • 3 Ent And Hn Surgery Department, AIIMS - All India Institute of Medical Sciences, 110029 - New Delhi/IN
  • 4 Radiation Oncology Department, AIIMS - All India Institute of Medical Sciences, 110029 - New Delhi/IN
  • 5 Surgical Oncology Department, AIIMS - All India Institute of Medical Sciences, 110029 - New Delhi/IN
  • 6 Radio-diagnosis Department, AIIMS - All India Institute of Medical Sciences, 110029 - New Delhi/IN
  • 7 Ent And Hn Surgery Department, Formerly at AIIMS - All India Institute of Medical Sciences, 110029 - New Delhi/IN

Resources

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Abstract 959P

Background

CTRT is used in eligible locally advanced (LA) SCCHN.

Methods

In a retrospective chart analysis and prospectively maintained database we analyzed data of LA SCCHN (nasopharynx excluded) treated between 2000-2016 and tried to find out prognostic factors for outcome by using appropriate methods. We use weekly cisplatin in dose of 40 mg/m2 weekly for a maximum of 7 weeks, and RT 70 Gy over 7 weeks. Baseline characteristics, treatment delivered, toxicities, response rates, and survival outcome were analysed. For purpose of analysis anyone who received at 5 weeks of cisplatin (200 mg/m2) and 6 weeks of radiation (30#) was considered to have received adequate therapy. Survival outcome was assessed in patients who received treatment. Telephonic contact or verbal autopsy was also carried out to retrieve information. Study was approved by IEC.

Results

1856 patients were considered for CTRT during this period. 1421 records were available. Median age was 51 yrs (14-72). Males were 1297. Primary sites; oropharynx (712), hypopharynx (195), larynx (286), and others (222). 622 had stage 3 and 795 had stage IV disease. 986 had node + disease. ECOG PS was 0 in 119, I in 708, and II in 494 patients. Albumin levels lower than normal was seen in 121 patients and 1157 had normal/higher levels. 1345 received treatment and included for survival analysis, outcome measures, and multi-variate analysis. 1072 (75.4%) patients received at least 5 doses of cisplatin, and 1201 (84.5%) received at least 30 # of radiation. 1071 (75.4%) patients completed treatment. Response was seen in 90.3% (67.8% CR). 330 (24.5%) required hospitalization for various reasons, 499 (37.1%) had treatment breaks. 513 (36.2%) are alive without disease and 635 (44.7%) died (38.9% due to disease and 3.3% due to toxicity). 3.9% developed second primary. Median OS was 54 months. On multi-variate, OS was significantly superior in patients with laryngeal primary, normal albumin, ECOG 0-1, females, stage III, and those who could complete planned treatment.

Conclusions

This large single center series highlights comparable results with CTRT in LA SCCHN. Survival was superior with laryngeal primary, normal albumin, and ECOG 0-1. Toxicity and tolerance was somewhat similar to other reports.

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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