TY - JOUR
T1 - Transoral robotic resection and reconstruction for head and neck cancer
AU - Genden, Eric M.
AU - Kotz, Tamar
AU - Tong, Charles C.L.
AU - Smith, Claris
AU - Sikora, Andrew G.
AU - Teng, Marita S.
AU - Packer, Stuart H.
AU - Lawson, William L.
AU - Kao, Johnny
PY - 2011/8/1
Y1 - 2011/8/1
N2 - Objectives/Hypothesis: To evaluate the patterns of failure, survival, and functional outcomes for patients treated with transoral robotic surgery (TORS) and compare these results with those from a cohort of patients treated with concurrent chemoradiation (CRT). Study Design: Prospective non-randomized case control study. Methods: Between April 2007 and April 2009, 30 patients with head and neck squamous cell carcinoma were treated with primary TORS and adjuvant therapy as indicated on an institutional review board-approved protocol. Patients were evaluated before treatment, after treatment, and at subsequent 3-month intervals after completing treatment to determine their disease and head and neck-specific functional status using the Performance Status Scale for Head and Neck Cancer and the Functional Oral Intake Score (FOIS). Functional scores were compared to a matched group of head and neck patients treated with primary CRT. Results: The TORS patient population included 73% stage III-IV and 23% nonsmokers. The median follow-up was 20.4 months (range, 12.8-39.6 months). The 18-month locoregional control, distant control, disease-free survival, and overall survival were 91%, 93%, 78%, and 90%, respectively. Compared to the primary CRT group, TORS was associated with better short-term eating ability (72 vs. 43, P =.008), diet (43 vs. 25, P =.01), and FOIS (5.5 vs. 3.3, P <.001) at 2 weeks after completion of treatment. In contrast to TORS patients who returned to baseline, the CRT group continued to have decreased diet (P =.03) and FOIS (P =.02) at 12 months. Conclusions: Our early experience in treating selected head and neck cancers with TORS is associated with excellent oncologic and functional outcomes that compare favorably to primary CRT.
AB - Objectives/Hypothesis: To evaluate the patterns of failure, survival, and functional outcomes for patients treated with transoral robotic surgery (TORS) and compare these results with those from a cohort of patients treated with concurrent chemoradiation (CRT). Study Design: Prospective non-randomized case control study. Methods: Between April 2007 and April 2009, 30 patients with head and neck squamous cell carcinoma were treated with primary TORS and adjuvant therapy as indicated on an institutional review board-approved protocol. Patients were evaluated before treatment, after treatment, and at subsequent 3-month intervals after completing treatment to determine their disease and head and neck-specific functional status using the Performance Status Scale for Head and Neck Cancer and the Functional Oral Intake Score (FOIS). Functional scores were compared to a matched group of head and neck patients treated with primary CRT. Results: The TORS patient population included 73% stage III-IV and 23% nonsmokers. The median follow-up was 20.4 months (range, 12.8-39.6 months). The 18-month locoregional control, distant control, disease-free survival, and overall survival were 91%, 93%, 78%, and 90%, respectively. Compared to the primary CRT group, TORS was associated with better short-term eating ability (72 vs. 43, P =.008), diet (43 vs. 25, P =.01), and FOIS (5.5 vs. 3.3, P <.001) at 2 weeks after completion of treatment. In contrast to TORS patients who returned to baseline, the CRT group continued to have decreased diet (P =.03) and FOIS (P =.02) at 12 months. Conclusions: Our early experience in treating selected head and neck cancers with TORS is associated with excellent oncologic and functional outcomes that compare favorably to primary CRT.
KW - Transoral robotic surgery
KW - head and neck cancer
KW - head and neck squamous cell carcinoma
KW - oropharyngeal cancer
KW - quality of life
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U2 - 10.1002/lary.21845
DO - 10.1002/lary.21845
M3 - Review article
C2 - 21792953
AN - SCOPUS:79960935331
SN - 0023-852X
VL - 121
SP - 1668
EP - 1674
JO - Laryngoscope
JF - Laryngoscope
IS - 8
ER -