Stereotactic Body Radiation Therapy for Stage IIA to IIIA Inoperable Non-Small Cell Lung Cancer: A Phase 1 Dose-Escalation Trial

被引:2
|
作者
Rimner, Andreas [1 ,2 ]
Gelblum, Daphna Y. [1 ]
Wu, Abraham J. [1 ]
Shepherd, Annemarie F. [1 ]
Mueller, Boris [1 ]
Zhang, Siyuan [1 ,3 ]
Cuaron, John [1 ]
Shaverdian, Narek
Flynn, Jessica [4 ]
Fiasconaro, Megan [4 ,5 ]
Zhang, Zhigang [4 ]
von Reibnitz, Donata [1 ,6 ]
Li, Henry [1 ]
McKnight, Dominique [1 ]
McCune, Megan [1 ]
Gelb, Emily [1 ]
Gomez, Daniel R. [1 ]
Simone, Charles B. [1 ]
Deasy, Joseph O. [7 ]
Yorke, Ellen D. [7 ]
Ng, Kenneth K. [8 ]
Chaft, Jamie E. [8 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, New York, NY 10065 USA
[2] Univ Freiburg, Dept Radiat Oncol, Robert Koch Str 3, D-79106 Freiburg, Germany
[3] Peking Univ Canc Hosp & Inst, Dept Radiat Oncol, Key Lab Carcinogenesis & Translat Res, Minist Educ Beijing, Beijing, Peoples R China
[4] Mem Sloan Kettering Canc Ctr, Dept Biostat, New York, NY USA
[5] Flatiron Hlth, New York, NY USA
[6] Stadtspital Waid, Dept Surg, Zurich, Switzerland
[7] Mem Sloan Kettering Canc Ctr, Dept Med Phys, New York, NY USA
[8] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY USA
关键词
CLINICAL-OUTCOMES; RADIOTHERAPY; CARCINOMA; TOXICITY; EFFICACY; TUMORS;
D O I
10.1016/j.ijrobp.2023.12.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Larger tumors are underrepresented in most prospective trials on stereotactic body radiation therapy (SBRT) for inoperable non-small cell lung cancer (NSCLC). We performed this phase 1 trial to speci fi cally study the maximum tolerated dose (MTD) of SBRT for NSCLC > 3 cm. Methods and Materials: A 3 + 3 dose-escalation design (cohort A) with an expansion cohort at the MTD (cohort B) was used. Patients with inoperable NSCLC > 3 cm (T2-4) were eligible. Select ipsilateral hilar and single-station mediastinal nodes were permitted. The initial SBRT dose was 40 Gy in 5 fractions, with planned escalation to 50 and 60 Gy in 5 fractions. Adjuvant chemotherapy was mandatory for cohort A and optional for cohort B, but no patients in cohort B received chemotherapy. The primary endpoint was SBRT-related acute grade (G) 4+ or persistent G3 toxicities (Common Terminology Criteria for Adverse Events version 4.03). Secondary endpoints included local failure (LF), distant metastases, disease progression, and overall survival. Results: The median age was 80 years; tumor size was > 3 cm and <= 5 cm in 20 (59%) and > 5 cm in 14 patients (41%). In cohort A (n = 9), 3 patients treated to 50 Gy experienced G3 radiation pneumonitis (RP), thus de fi ning the MTD. In the larger dose-expansion cohort B (n = 25), no radiation therapy - related G4+ toxicities and no G3 RP occurred; only 2 patients experienced G2 RP. The 2-year cumulative incidence of LF was 20.2%, distant failure was 34.7%, and disease progression was 54.4%. Two-year overall survival was 53%. A biologically effective dose (BED) < 100 Gy was associated with higher LF ( P = .006); advanced stage and higher neutrophil/lymphocyte ratio were associated with greater disease progression (both P = .004). Conclusions: Fifty Gy in 5 fractions is the MTD for SBRT to tumors > 3 cm. A higher BED is associated with fewer LFs even in larger tumors. Cohort B appears to have had less toxicity, possibly due to the omission of chemotherapy. (c) 2023 Elsevier Inc. All rights reserved.
引用
收藏
页码:869 / 877
页数:9
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