Volumetric-Modulated Arc-Based Re-radiosurgery With Simultaneous Reduced-Dose Whole-Brain Irradiation for Local Failures Following Prior Radiosurgery of Brain Oligometastases From Small Cell Lung Cancer

被引:5
作者
Ohtakara, Kazuhiro [1 ,2 ]
Arakawa, Sosuke [3 ,4 ]
Nakao, Makoto [4 ]
Muramatsu, Hideki [4 ]
Suzuki, Kojiro [2 ]
机构
[1] Kainan Hosp Aichi Prefectural Welf Federat Agr Coo, Dept Radiat Oncol, Yatomi, Japan
[2] Aichi Med Univ, Dept Radiol, Nagakute, Japan
[3] Nagoya City Univ, Dept Resp Med, East Med Ctr, Nagoya, Japan
[4] Kainan Hosp Aichi Prefectural Welf Federat Agr Coo, Dept Resp Med, Yatomi, Japan
关键词
volumetric-modulated arc-based radiosurgery; simultaneous integrated boost; fractionation; biological effective dose; re-irradiation; stereotactic radiosurgery; limited-stage; chemoradiotherapy; small cell lung cancer; brain metastases; RADIATION-THERAPY; METASTASES; RADIOTHERAPY;
D O I
10.7759/cureus.44492
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
First -line and possibly repeated stereotactic radiosurgery (SRS) with preserving whole-brain radiotherapy (WBRT) is an attractive and promising option for synchronous or metachronous limited brain metastases (BMs) from small cell lung cancer (SCLC), for which a modest prescription dose is generally preferred, such as a biological effective dose of <= 60 Gy, based on the linear-quadratic formula with an alpha/beta ratio of 10 (BED10). In addition, the optimal planning scheme for re -SRS for local progression after SRS of BMs from SCLC remains unclear. Herein, we describe a case of limited BMs developing after a partial response to standard chemoradiotherapy (CRT) for limited-stage SCLC. The BMs, including local failures following prior single-fraction (fr) SRS, were re-treated with volumetric-modulated arc-based SRS combined with simultaneous reduced-dose WBRT. The first SRS with 36.3 Gy/3 fr (BED10 80 Gy) for a small BM resulted in a local control of 17.2 months. However, the second SRS with 20 Gy/1 fr (BED10 60 Gy) to the 60% or 85% isodose surface (IDS) covering the gross tumor volume (GTV) of three new BMs with a paradoxical T1/T2 mismatch, that is, a visible mass on T2 larger than an enhancing area, resulted in partial symptomatic local progression of all lesions within 5.2 months, along with the development of two new lesions, despite continued amrubicin monotherapy. In contrast, the third SRS with 53 Gy/10 fr (BED10 81 Gy) to <= 74% IDSs encompassing the GTV boundary resulted in complete responses of all the lesions during six months. However, despite a combined use of WBRT of 25 Gy in the third SRS, symptomatic spinal cerebrospinal fluid dissemination and new BMs developed, the former leading to patient mortality. A BED10 of >= 80 Gy to the GTV margin and a steep dose increase inside the GTV boundary are suitable to ensure excellent local control in SRS for SCLC BMs. Re -SRS with the aforementioned scheme can be an efficacious option for local failures following prior SRS with a BED10 of <= 60 Gy. Modest dose escalation with a simultaneous integrated boost to bulky lesions in the initial CRT may reduce the development of new BM through improved control of the potential source.
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页数:15
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