# Treatment with (chemo)-radiation in old patients (≥76 years of age) with newly diagnosed non-metastatic squamous cell cancer of the head and neck region: real-world data from a tertiary referral center

**Authors:** Leah-Sophie Winkler, Marlen Haderlein, Sabine Semrau, Florian Putz, Daniel Höfler, Sarina K. Müller, Heinrich Iro, Marco Kesting, Rainer Fietkau, Philipp Schubert

PMC · DOI: 10.3389/fonc.2024.1382405 · Frontiers in Oncology · 2024-04-25

## TL;DR

This study examines treatment outcomes for elderly patients with newly diagnosed head and neck cancer, finding that oropharyngeal tumor location is linked to better survival and fewer recurrences.

## Contribution

The study provides real-world data on treatment outcomes and deviations from guidelines in elderly patients with HNSCC.

## Key findings

- Oropharyngeal tumor localization significantly improves overall and progression-free survival in elderly HNSCC patients.
- Combined treatment (surgery and postoperative therapy) is associated with better progression-free survival.
- Non-oropharyngeal tumor location is a risk factor for decreased survival and higher recurrence rates.

## Abstract

Treatment of patients with cancer of the head and neck region is in focus in a multitude of studies. Of these patients, one patient group, those aged 76 and more, is mostly underrepresented despite requiring thorough and well-reasoned treatment decisions to offer curative treatment. This study investigates real-world data on curative treatment of old (≥76 years) patients with newly diagnosed squamous cell carcinoma of the head and neck region (HNSCC).

Between January 2010 and December 2021, we identified 71 patients older than 76 years with newly diagnosed HNSCC and cM0 at the Department of Radiation Oncology of the University Hospital of Erlangen-Nuremberg. Using electronic medical records, we analyzed treatment patterns and outcomes in terms of overall survival (OS), progression-free survival (PFS), and locoregional control (LRC) rate. Additionally, we performed univariate risk analysis and Cox regression in order to identify predictive factors associated with the abovementioned treatment outcomes.

The median follow-up was 18 months. OS was 83%, 79%, and 72% after 1 year, 2 years, and 3 years, respectively. PFS was 69%, 54%, and 46% after 1 year, 2 years, and 3 years, respectively. A total of 34 (48%) patients were treated with standard therapy according to current guidelines. The reasons for deviation from standard therapy before or during treatment were as follows: unfitness for cisplatin-based chemotherapy (n = 37), reduction of chemotherapy (n = 3), and dose reduction/interruption of radiotherapy (n = 8). Carboplatin-based systemic therapy showed improved PFS compared to cisplatin or cetuximab (60 vs. 28 vs. 15 months, p = 0.037) but without impact on OS (83 vs. 52 vs. 38 months, p = 0.807). Oropharyngeal tumor localization (p = 0.026) and combined treatment (surgery and postoperative treatment) (p = 0.008) were significant predictors for a better OS. In multivariate analysis, oropharyngeal tumor localization (p = 0.011) and combined treatment (p = 0.041) showed significantly increased PFS. After 1 year, 2 years, and 3 years, the cumulative incidence of locoregional recurrences (LRRs) was 13%, 24%, and 27%, respectively, and was significantly decreased in patients with oropharyngeal tumor localization (p = 0.037).

Adherence to treatment protocols for radiotherapy alone in old patients with HNSCC is good, whereas the application of concurrent chemotherapy often deviates from guidelines in terms of de-escalation. An important risk factor for decreased OS, PFS, and a higher rate of LRR appears to be non-oropharyngeal tumor location in old patients.

## Linked entities

- **Chemicals:** cisplatin (PubChem CID 5460033), carboplatin (PubChem CID 426756)
- **Diseases:** HNSCC (MONDO:0010150)

## Full-text entities

- **Diseases:** cancer of the head and neck region (MESH:D006258), HNSCC (MESH:D000077195), Oropharyngeal tumor (MESH:D009959)
- **Chemicals:** Carboplatin (MESH:D016190), cisplatin (MESH:D002945), cetuximab (MESH:D000068818)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11079188/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC11079188/full.md

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Source: https://tomesphere.com/paper/PMC11079188