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A phase I/II trial of concurrent immunotherapy with chemoradiation in locally advanced larynx cancer.
Frankart, Andrew J; Sadraei, Nooshin Hashemi; Huth, Brad; Redmond, Kevin P; Barrett, William L; Kurtzweil, Nicky; Riaz, Muhammad K; Wise-Draper, Trisha; Rodriguez, Cristina P; Adelstein, David J; Takiar, Vinita.
Afiliação
  • Frankart AJ; Department of Radiation Oncology University of Cincinnati Cincinnati Ohio USA.
  • Sadraei NH; Division of Hematology/Oncology University of Cincinnati Cincinnati Ohio USA.
  • Huth B; Department of Radiation Oncology University of Cincinnati Cincinnati Ohio USA.
  • Redmond KP; Department of Radiation Oncology University of Cincinnati Cincinnati Ohio USA.
  • Barrett WL; Department of Radiation Oncology University of Cincinnati Cincinnati Ohio USA.
  • Kurtzweil N; University of Cincinnati Cancer Center Cincinnati Ohio USA.
  • Riaz MK; Division of Hematology/Oncology University of Cincinnati Cincinnati Ohio USA.
  • Wise-Draper T; Division of Hematology/Oncology University of Cincinnati Cincinnati Ohio USA.
  • Rodriguez CP; Division of Oncology, Department of Medicine University of Washington Seattle Washington USA.
  • Adelstein DJ; Department of Hematology and Medical Oncology Cleveland Clinic Taussig Cancer Institute Cleveland Ohio USA.
  • Takiar V; Department of Radiation Oncology University of Cincinnati Cincinnati Ohio USA.
Laryngoscope Investig Otolaryngol ; 7(2): 437-443, 2022 Apr.
Article em En | MEDLINE | ID: mdl-35434343
ABSTRACT

Objectives:

Cisplatin-based chemoradiation is an established organ-preserving strategy for locally advanced laryngeal cancer, but long-term survival remains suboptimal. Immunotherapy has been studied in the metastatic and unresectable recurrent settings. However, additional data are needed to assess its role in organ preservation for locally advanced laryngeal cancer.

Methods:

This trial was an open-label, single-arm, multi-institutional study with a Phase I run-in portion followed by a planned Phase II component, which closed early due to low accrual. Study patients had Stage III or IV (T2-3; N0-3; M0) laryngeal squamous cell carcinoma and were candidates for larynx preservation. Pembrolizumab was given 2-3 weeks prior to chemoradiation and then, q21 days concurrently with high-dose cisplatin and radiation prescribed to a total dose of 70 Gy. The primary endpoint of the trial was organ-preservation rate (OPR) at 18 months.

Results:

A total of nine patients were enrolled with a median follow-up of 30.1 months. No patient required laryngectomy, resulting in 100% OPR at 18 months. The 12-month overall survival (OS) rate was 77.8% and the median duration of OS was not reached. All acute Grade 4 (n = 3) toxicities occurred in a single patient with poorly controlled diabetes at baseline. One patient had late Grade 4 laryngeal edema requiring tracheostomy 8 months after chemoradiation, which self-resolved.

Conclusion:

UCCI-HN-15-02 demonstrated the safety of the addition of immunotherapy to definitive chemoradiation and the patient outcomes suggest the potential for improving long-term survival while minimizing negative impact from treatment. While results from this trial were promising, a randomized study with a larger number of patients and longer follow-up is warranted to verify this treatment approach prior to wider adoption. NCT # NCT02759575.Level of evidence 2b.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Revista: Laryngoscope Investig Otolaryngol Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Clinical_trials Idioma: En Revista: Laryngoscope Investig Otolaryngol Ano de publicação: 2022 Tipo de documento: Article