A Phase II Study of Accelerated Hyperfractionated Thoracic Radiotherapy With Dose Escalation to 54 Gy With Concurrent Cisplatin and Etoposide for Limited-Stage Small-Cell Lung Cancer: Long-Term Results at a Single Institution.

IF 3.3 3区 医学 Q2 ONCOLOGY
Kanji Matsuura, Ritsuko Komaki, Miho Kono, Tsuyoshi Kudo, Ayaka Ono, Tsubasa Kameoka, Ikumi Shintani, Hayate Kusaba, Atsushi Kawakubo, Yasuharu Ando, Kiyoto Nishihara, Yasuo Iwamoto, Hiroyasu Shoda, Tsuyoshi Katsuta, Masayuki Kagemoto
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引用次数: 0

Abstract

Purpose: The combination of 45 Gy accelerated hyperfractionated thoracic radiotherapy (AHF-TRT) and concurrent chemotherapy is the standard treatment for limited-stage small-cell lung cancer (LS-SCLC). However, the optimal dose and fractionation remain controversial. We herein report the long-term results of a phase II study investigating the utility of dose escalation to 54 Gy in AHF-TRT for LS-SCLC.

Methods and materials: We enrolled patients with pathologically confirmed LS-SCLC. The radiation dose was 54 Gy, delivered in 36 fractions over 3.6 weeks. All patients were treated with 3D-CRT with multiple fields to reduce the elevated dose volume to the surrounding tissues. The chemotherapy regimens consisted of either cisplatin and etoposide or carboplatin and etoposide. All patients were evaluated for overall survival (OS), progression-free survival (PFS), and nonhematological toxicity.

Results: Between 2013 and 2019, 21 patients were enrolled in this study. All the patients were assessed for their response and toxicities. The median age was 70 years and 15 patients were male, while 6 were female. The median follow-up period of all patients was 57.3 months. The 2- and 5-year OS rates were 85.7% and 47.6% respectively. The 2- and 5-year PFS rates were 52.3% and 47.6% respectively. No patient experienced grade ≥ 3 nonhematological adverse effects either during treatment or in follow-up.

Conclusions: In this phase II study, AHF-TRT of 54 Gy resulted in a good OS and PFS without increasing severe toxicities. These outcomes suggest that dose escalation to 54 Gy may be a promising radical treatment for LS-SCLC.

一项加速胸部超分割放疗的II期研究,剂量增加到54 Gy,同时使用顺铂和依托泊苷治疗有限期小细胞肺癌:单一机构的长期结果。
目的:45 Gy加速胸部超分割放疗(AHF-TRT)联合同期化疗是有限期小细胞肺癌(LS-SCLC)的标准治疗方案。然而,最佳剂量和分离仍然存在争议。我们在此报告了一项II期研究的长期结果,该研究调查了剂量递增至54 Gy的AHF-TRT治疗LS-SCLC的效用。方法和材料:我们招募了病理证实的LS-SCLC患者。放射剂量为54戈瑞,在3.6周内分36次给予。所有患者均行多场3D-CRT治疗,以减少升高剂量对周围组织的影响。化疗方案由顺铂和依托泊苷或卡铂和依托泊苷组成。对所有患者进行总生存期(OS)、无进展生存期(PFS)和非血液学毒性评估。结果:2013年至2019年,21名患者入组本研究。对所有患者的反应和毒性进行评估。中位年龄70岁,男性15例,女性6例。所有患者的中位随访时间为57.3个月。2年和5年OS分别为85.7%和47.6%。2年和5年PFS分别为52.3%和47.6%。在治疗或随访期间,没有患者出现≥3级的非血液学不良反应。结论:在这项II期研究中,54 Gy的AHF-TRT可获得良好的OS和PFS,且未增加严重毒性。这些结果表明,剂量增加到54 Gy可能是一种很有希望的LS-SCLC根治性治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical lung cancer
Clinical lung cancer 医学-肿瘤学
CiteScore
7.00
自引率
2.80%
发文量
159
审稿时长
24 days
期刊介绍: Clinical Lung Cancer is a peer-reviewed bimonthly journal that publishes original articles describing various aspects of clinical and translational research of lung cancer. Clinical Lung Cancer is devoted to articles on detection, diagnosis, prevention, and treatment of lung cancer. The main emphasis is on recent scientific developments in all areas related to lung cancer. Specific areas of interest include clinical research and mechanistic approaches; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; and integration of various approaches.
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