Intensity-modulated radiation therapy with concurrent chemotherapy followed by durvalumab for stage III non-small cell lung cancer: A multi-center retrospective study

被引:36
作者
Tsukita, Yoko [1 ]
Yamamoto, Takaya [2 ]
Mayahara, Hiroshi [3 ]
Hata, Akito [4 ]
Takeda, Yuichiro [5 ]
Nakayama, Hidetsugu [6 ]
Tanaka, Satoshi [7 ]
Uchida, Junji [7 ]
Usui, Kazuhiro [8 ]
Toyoda, Tatsuya [9 ]
Tamiya, Motohiro [10 ]
Morimoto, Masahiro [11 ]
Oya, Yuko [12 ]
Kodaira, Takeshi [13 ]
Miyauchi, Eisaku [1 ]
Jingu, Keiichi [2 ]
Sugiura, Hisatoshi [1 ]
机构
[1] Tohoku Univ, Dept Resp Med, Grad Sch Med, Sendai, Miyagi, Japan
[2] Tohoku Univ, Dept Radiat Oncol, Grad Sch Med, Sendai, Miyagi, Japan
[3] Kobe Minimally Invas Canc Ctr, Dept Radiat Oncol, Kobe, Hyogo, Japan
[4] Kobe Minimally Invas Canc Ctr, Dept Resp Med Oncol, Kobe, Hyogo, Japan
[5] Natl Ctr Global Hlth & Med, Dept Resp Med, Tokyo, Japan
[6] Natl Ctr Global Hlth & Med, Dept Radiat Oncol, Tokyo, Japan
[7] Osaka Gen Med Ctr, Dept Resp Med, Osaka, Japan
[8] NTT Med Ctr Tokyo, Div Respirol, Tokyo, Japan
[9] NTT Med Ctr Tokyo, Dept Radiol, Tokyo, Japan
[10] Osaka Int Canc Inst, Dept Thorac Oncol, Osaka, Japan
[11] Osaka Int Canc Inst, Dept Radiat Oncol, Osaka, Japan
[12] Aichi Canc Ctr Hosp, Dept Thorac Oncol, Nagoya, Aichi, Japan
[13] Aichi Canc Ctr Hosp, Dept Radiat Oncol, Nagoya, Aichi, Japan
关键词
NSCLC; IMRT; Chemoradiotherapy; Pneumonitis; Durvalumab; RANDOMIZED PHASE-II; PNEUMONITIS; RADIOTHERAPY; CHEMORADIOTHERAPY; CONSOLIDATION; CISPLATIN; CHEMORADIATION; VINORELBINE; TRIAL; SCORE;
D O I
10.1016/j.radonc.2021.05.016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and purpose: Intensity-modulated radiation therapy (IMRT) is increasingly applied in concur-rent chemoradiotherapy (CCRT) for locally-advanced non-small cell lung cancer (NSCLC), with improve-ment of target coverage and better sparing of normal tissue. IMRT tends to have a larger low-dose irradiation volume than 3D conformal radiotherapy, but the incidence of and risk factors for pneumonitis remain unclear, especially following the approval of durvalumab. Materials and methods: We retrospectively reviewed the records of NSCLC patients treated by CCRT using IMRT at seven Japanese institutions. Primary outcomes were incidence of symptomatic pneumonitis and progression-free survival (PFS). Multivariate logistic regression analysis was used to identify risk factors for >grade 2 pneumonitis. Results: Median follow-up from the start of CCRT was 14.3 months (n = 107 patients; median age 70 years, 29% female). Median lung V5 and V20 was 49.2% and 19.5%, respectively. Durvalumab was administered to 87 patients (81%). Pneumonitis developed in 95 (89%) patients of which 53% had grade 1, 28% grade 2, 6.5% grade 3, and 0.9% grade 4. Durvalumab had been discontinued in 16 patients (18.4%) due to pneu-monitis. By multivariate analysis, age >70 years, male sex, and V5 >58.9% were identified as significantly associated with >grade 2 pneumonitis (p = 0.0065, 0.036 and 0.0013 respectively). The median PFS from the start of CCRT was not reached (95% CI, 14.2 months to not reached) in patients receiving durvalumab. Conclusion: CCRT using IMRT followed by durvalumab was generally effective and tolerable; V5 <60% would be recommended to avoid symptomatic pneumonitis. (c) 2021 Elsevier B.V. All rights reserved. Radiotherapy and Oncology 160 (2021) 266-272
引用
收藏
页码:266 / 272
页数:7
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