Risk of recurrence after neoadjuvant chemotherapy and transoral robotic surgery in patients with oropharynx cancer that avoid adjuvant radiation
Background De‐escalation strategies for newly‐diagnosed p16‐positive oropharyngeal squamous cell carcinoma (p16+ OPSCC), aim to reduce treatment‐related morbidity without compromising disease control. One strategy is neoadjuvant cisplatin and docetaxel chemotherapy (NAC + S) before transoral robotic...
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Veröffentlicht in: | Cancer medicine (Malden, MA) MA), 2024-04, Vol.13 (7), p.e7146-n/a |
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Zusammenfassung: | Background De‐escalation strategies for newly‐diagnosed p16‐positive oropharyngeal squamous cell carcinoma (p16+ OPSCC), aim to reduce treatment‐related morbidity without compromising disease control. One strategy is neoadjuvant cisplatin and docetaxel chemotherapy (NAC + S) before transoral robotic surgery, with pathology‐based risk‐adapted adjuvant treatment.
Methods We examined the recurrence‐free survival (RFS) for patients who received NAC + S.
Results Comparing outcomes in 103 patients between 2008 and 2023, 92% avoided adjuvant treatment and showed significantly higher 2‐year recurrence‐free survival (RFS) compared to those with adjuvant treatment (95.9% vs. 43.8%, p = 0.0049)
Conclusion Our findings suggest that pathology‐based risk‐adapted omission of adjuvant treatment following NAC + S does not appear to elevate recurrence risk and that NAC may identify patients with favorable tumor biology, yielding a 2‐year RFS probability exceeding 95% without adjuvant treatment. Further, the study identifies a patient subset experiencing disease recurrence despite triple modality therapy. Despite limitations, including a retrospective design and modest sample size, the data advocate for controlled NAC + S studies.
In appropriately selected patients with p16+ oropharyngeal squamous cell cancer, the administration of chemotherapy before surgery may lead to pathologic responses that allow the omission of postoperative adjuvant radiotherapy. In this retrospective study, we find that this omission did not adversely impact the recurrence‐free survival of patients. |
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ISSN: | 2045-7634 2045-7634 |
DOI: | 10.1002/cam4.7146 |