A benchmark for oncologic outcomes and model for lethal recurrence risk after transoral robotic resection of HPV-related oropharyngeal cancers.
A benchmark for oncologic outcomes and model for lethal recurrence risk after transoral robotic resection of HPV-related oropharyngeal cancers.
复制标题
经口机器人切除HPV相关口咽癌后肿瘤学结局的基准和致命复发风险模型
DOI:
10.1016/j.oraloncology.2022.105798
复制
发表时间:
2022-04
期刊:
影响因子:
4.8
通讯作者:
Basu, Devraj
中科院分区:
文献类型:
--
作者:
Brody, Robert M.;Shimunov, David;Cohen, Roger B.;Lin, Alexander;Lukens, John N.;Hartner, Lee;Aggarwal, Charu;Duvvuri, Umamaheswar;Montone, Kathleen T.;Jalaly, Jalal B.;LiVolsi, Virginia A.;Carey, Ryan M.;Shanti, Rabie M.;Rajasekaran, Karthik;Chalian, Ara A.;Rassekh, Christopher H.;Cannady, Steven B.;Newman, Jason G.;O'Malley, Bert W.;Weinstein, Gregory S.;Gimotty, Phyllis A.;Basu, Devraj
关键词:
Increasing use of transoral robotic surgery (TORS) is likely to impact outcomes for HPV+ oropharyngeal squamous cell carcinomas (OPSCCs). We aimed to describe oncologic outcomes for a large HPV+ OPSCC cohort after TORS and develop a risk prediction model for recurrence under this treatment paradigm. 634 HPV+ OPSCC patients receiving TORS-based therapy at a single institution were reviewed retrospectively to describe survival across the entire cohort and for patients suffering recurrence. Risks for distant metastatic recurrence (DMR) and locoregional recurrence (LRR) were modeled using multivariate logistic regression analyses of case-control sub-cohorts. 5-year overall and recurrence-free survival were 91.2% and 86.1%, respectively. 5-year overall survival was 52.5% following DMR and 83.3% after isolated LRR (P=.01). In case-control analyses, positive surgical margins were associated with DMR (adjusted OR 5.8, CI 2.1–16.0, P=.001), but not isolated LRR, and increased DMR risk 4.2 fold in patients with early clinical stage disease. By contrast, LRR was associated with not receiving recommended adjuvant therapy (OR 13.4, CI 6.3–28.5, P<.001). This study sets a benchmark for oncologic outcomes from HPV+ OPSCC after TORS-based therapy. Under this treatment paradigm, margins are relevant for assessing lethal recurrence risk during clinical trial design and post-treatment surveillance.
登录
查看更多内容
影响因子:
8.4
作者:
Eisenhauer, E. A.;Therasse, P.;Verweij, J.
通讯作者:
Verweij, J.
影响因子:
6.2
作者:
Cracchiolo JR;Baxi SS;Morris LG;Ganly I;Patel SG;Cohen MA;Roman BR
通讯作者:
Roman BR
影响因子:
4.8
作者:
Haughey BH;Sinha P;Kallogjeri D;Goldberg RL;Lewis JS Jr;Piccirillo JF;Jackson RS;Moore EJ;Brandwein-Gensler M;Magnuson SJ;Carroll WR;Jones TM;Wilkie MD;Lau A;Upile NS;Sheard J;Lancaster J;Tandon S;Robinson M;Husband D;Ganly I;Shah JP;Brizel DM;O'Sullivan B;Ridge JA;Lydiatt WM
通讯作者:
Lydiatt WM
影响因子:
168.9
作者:
Mehanna, Hisham;Robinson, Max;Dunn, Janet
通讯作者:
Dunn, Janet
影响因子:
8
作者:
Harbison, R. Alex;Kubik, Mark;Mendez, Eduardo
通讯作者:
Mendez, Eduardo