Selective Treatment Deintensification by Reducing Radiation Dose and Omitting Concurrent Chemotherapy Based on Response to Induction Chemotherapy in Human Papillomavirus-Associated Oropharyngeal Squamous Cell Carcinoma: A Single-Arm, Phase 2 Trial (IChoice-01)

被引:9
|
作者
Xu, Tingting [1 ,2 ,3 ,4 ]
Shen, Chunying [1 ,2 ,3 ,4 ]
Zhou, Xin [1 ,2 ,3 ,4 ]
Zhu, Lin [1 ,2 ,3 ,4 ]
Xiang, Jun [5 ]
Wang, Yulong [5 ]
Zhu, Yongxue [5 ]
He, Xiayun [1 ,2 ,3 ,4 ]
Ying, Hongmei [1 ,2 ,3 ,4 ]
Wang, Yu [5 ]
Ji, Qinghai [5 ]
Hu, Chaosu [1 ,2 ,3 ,4 ]
Lu, Xueguan [1 ,2 ,3 ,4 ]
机构
[1] Fudan Univ, Shanghai Canc Ctr, Dept Radiat Oncol, Shanghai, Peoples R China
[2] Fudan Univ, Shanghai Med Coll, Dept Oncol, Shanghai, Peoples R China
[3] Shanghai Clin Res Ctr Radiat Oncol, Dept Radiat Oncol, Shanghai, Peoples R China
[4] Shanghai Key Lab Radiat Oncol, Shanghai, Peoples R China
[5] Fudan Univ, Shanghai Canc Ctr, Dept Head & Neck Surg, Shanghai, Peoples R China
关键词
LOCALLY ADVANCED LARYNX; TAX; 324; CANCER; SURVIVAL; THERAPY; HEAD; CHEMORADIOTHERAPY; CETUXIMAB;
D O I
10.1016/j.ijrobp.2023.07.037
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To demonstrate the feasibility of deintensification regimen in the light of the response to induction chemotherapy (IC) in human papillomavirus (HPV)-associated oropharyngeal squamous cell carcinoma (OPSCC).Methods and Materials: Patients with p16+ OPSCC, T1-2/N1-3M0 (excluding T1N1M0 with single and <= 3 cm lymph node) or T3-4N0-3M0 were enrolled between January 2019 and July 2021. All patients received 2 cycles of IC with docetaxel 75 mg/m2 dL and cisplatin 75 mg/m2 dL every 3 weeks. Those with major responses (>= 50% decrease in both primary and lymph nodes) to IC entered the deintensification cohort (cohort D), in which intensity modulated radiation therapy alone was given to a reduced dose of 60 Gy/30 fractions. Those who failed to meet major responsesentered the concurrent chemoradiotherapy cohort (cohort C), where the dose was simultaneously integrated boosted to a standard 70 Gy/35 fractions to nonmajor response sites, concurrently with cisplatin 80 mg/m2 dL,22. Patient-reported swallow function was documented using the MD Anderson Dysphagia Inventory. The primary endpoint was 2-year progression-free survival (PFS) using Simon's 2 stage design.Results: A total of 26 of 48 (54.2%) participants met the criteria to enter cohort D and 22 of 48 (45.8%) patients entered cohort C. With a median follow-up time of 29.7 months (6.9-48.0 months), 2-year PFS and OS rates were 85.4% and 93.6%, respectively for all enrolled patients. In cohort D, 2-year PFS and OS rates were both 100%. Grade 3 and 4 IC-related toxicities included leukopenia/neutropenia occurring in 41.7% and hyponatremia in 4.2% of patients. A higher incidence of grade 3 and 4 mucositis (61.9% vs 23.1% P = .022) was observed in cohort C. Consistent decline in longitudinal MD Anderson Dysphagia Inventory scores were observed at month 3 after radiation therapy between cohorts and both were found to recover to baseline at month 12.Conclusions: Selective radiation therapy dose reduction and concurrent chemotherapy removal based on IC response in HPV + OPSCC was feasible and promising. Further study of this strategy to balance efficacy and toxicity is warranted in a prospective controlled trial.(c) 2023 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
引用
收藏
页码:169 / 178
页数:10
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