Prognostic impact of bridge or neoadjuvant induction chemotherapy in patients with resected oral cavity cancer: A nationwide cohort study

Author:

Hsu Cheng‐Lung1,Wen Yu‐Wen23,Wang Hung‐Ming1,Hsieh Chia‐Hsun1ORCID,Liao Chi‐Ting1,Lee Li‐Yu4,Ng Shu‐Hang5,Lin Chien‐Yu6ORCID,Chen Wen‐Cheng7ORCID,Lin Jin‐Ching8ORCID,Tsai Yao‐Te9,Lee Shu‐Ru10,Chien Chih‐Yen11ORCID,Hua Chun‐Hung12,Wang Cheng Ping13,Chen Tsung‐Ming14,Terng Shyuang‐Der15,Tsai Chi‐Ying16,Fan Kang‐Hsing17,Yeh Chih‐Hua5ORCID,Lin Chih‐Hung18,Tsao Chung‐Kan18,Cheng Nai‐Ming19,Fang Tuan‐Jen20,Huang Shiang‐Fu20,Kang Chung‐Jan20ORCID,Lee Li‐Ang20,Fang Ku‐Hao20,Wang Yu‐Chien20,Lin Wan‐Ni20,Hsin Li‐Jen20,Yen Tzu‐Chen19,Liao Chun‐Ta20ORCID

Affiliation:

1. Department of Medical Oncology Chang Gung Memorial Hospital and Chang Gung University Taoyuan Taiwan

2. Clinical Informatics and Medical Statistics Research Center Chang Gung University Taoyuan Taiwan

3. Division of Thoracic Surgery Chang Gung Memorial Hospital Taoyuan Taiwan

4. Department of Pathology Chang Gung Memorial Hospital and Chang Gung University Taoyuan Taiwan

5. Department of Diagnostic Radiology Chang Gung Memorial Hospital and Chang Gung University Taoyuan Taiwan

6. Department of Radiation Oncology Chang Gung Memorial Hospital and Chang Gung University Taoyuan Taiwan

7. Department of Radiation Oncology Chang Gung Memorial Hospital Chiayi Taiwan

8. Department of Radiation Oncology Changhua Christian Hospital Changhua Taiwan

9. Department of Otorhinolaryngology‐Head and Neck Surgery Chang Gung Memorial Hospital Chiayi Taiwan

10. Research Service Center for Health Information Chang Gung University Taoyuan Taiwan

11. Department of Otolaryngology, Chang Gung Memorial Hospital Kaohsiung Medical Center Chang Gung University College of Medicine Kaohsiung Taiwan

12. Department of Otorhinolaryngology China Medical University Hospital Taichung Taiwan

13. Department of Otolaryngology National Taiwan University Hospital and College of Medicine Taipei Taiwan

14. Department of Otolaryngology Shuang Ho Hospital, Taipei Medical University New Taipei City Taiwan

15. Department of Head and Neck Surgery Koo Foundation Sun Yat‐Sen Cancer Center Taipei Taiwan

16. Department of Oral and Maxillofacial Surgery Chang Gung Memorial Hospital, Chang Gung University Taoyuan Taiwan

17. Department of Radiation Oncology New Taipei Municipal TuCheng Hospital New Taipei City Taiwan

18. Department of Plastic and Reconstructive Surgery Chang Gung Memorial Hospital and Chang Gung University Taoyuan Taiwan

19. Department of Nuclear Medicine and Molecular Imaging Center Chang Gung Memorial Hospital and Chang Gung University Taoyuan Taiwan

20. Department of Otorhinolaryngology, Head and Neck Surgery Chang Gung Memorial Hospital and Chang Gung University Taoyuan Taiwan

Abstract

AbstractBackgroundWhile surgery remains the primary treatment for oral squamous cell carcinoma (OCSCC), induction chemotherapy (IC) can be used as a bridging or neoadjuvant therapy. This nationwide study in Taiwan examines the survival outcomes of OCSCC patients who received IC before surgery.MethodsWe analyzed data from 29,891 patients with OCSCC. Of these, 29,058 initially underwent surgery (OP group), whereas 833 received IC before surgery (IC + OP group). A propensity score (PS)‐matched analysis (4, 1 ratio, 3260 vs. 815 patients) was performed considering tumor subsite, sex, age, Charlson comorbidity index, clinical T1–T4b tumors, clinical N0–3 disease, and clinical stage I–IV.ResultsIn the PS‐matched cohort, the 5‐year disease‐specific survival (DSS) and overall survival (OS) rates were 65% and 57%, respectively. When comparing the OP and IC + OP groups, the 5‐year DSS rates were 66% and 62%, respectively (p = 0.1162). Additionally, the 5‐year OS rates were 57% and 56%, respectively (p = 0.9917). No significant intergroup differences in survival were observed for specific subgroups with cT4a tumors, cT4b tumors, cN3 disease, pT4b tumors, and pN3 disease. However, for patients with pT4a tumors, the OP group demonstrated superior 5‐year outcomes compared to the IC + OP group, with a DSS of 62% versus 52% (p = 0.0006) and an OS of 53% versus 44% (p = 0.0060). Notably, patients with cT2–3, cN1, and c‐Stage II disease in the IC + OP group were significantly more likely to achieve pT0–1 status (p < 0.05).ConclusionsFollowing PS matching, the IC + OP group generally exhibited similar prognosis to the OP group. However, for pT4a tumors, the OP group showed superior 5‐year outcomes. While IC may not universally improve survival, it could be advantageous for patients who respond positively to the treatment.

Publisher

Wiley

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