The efficacy profiles of concurrent chemoradiotherapy with intensity-modulated radiotherapy followed by durvalumab in patients with unresectable stage III non–small cell lung cancer: A multicenter retrospective cohort study. (November 2022)
- Record Type:
- Journal Article
- Title:
- The efficacy profiles of concurrent chemoradiotherapy with intensity-modulated radiotherapy followed by durvalumab in patients with unresectable stage III non–small cell lung cancer: A multicenter retrospective cohort study. (November 2022)
- Main Title:
- The efficacy profiles of concurrent chemoradiotherapy with intensity-modulated radiotherapy followed by durvalumab in patients with unresectable stage III non–small cell lung cancer: A multicenter retrospective cohort study
- Authors:
- Takeda, Yuichiro
Kusaba, Yusaku
Tsukita, Yoko
Uemura, Yukari
Miyauchi, Eisaku
Yamamoto, Takaya
Mayahara, Hiroshi
Hata, Akito
Nakayama, Hidetsugu
Tanaka, Satoshi
Uchida, Junji
Usui, Kazuhiro
Toyoda, Tatsuya
Tamiya, Motohiro
Morimoto, Masahiro
Oya, Yuko
Kodaira, Takeshi
Jingu, Keiichi
Sugiura, Hisatoshi - Abstract:
- Highlights: The tri-modalities of chemoradiotherapy (CRT) with IMRT and durvalumab were evaluated. We have reported the efficacy and safety of tri-modalities through real-world data. A better response to CRT and increasing radiation dose are related to long PFS. Durvalumab therapy duration was linked to survival in patients. Abstract: Purpose: Intensity-modulated radiotherapy (IMRT) is currently used more commonly than 3-dimensional conformal radiation for definitive thoracic radiation. We examined the efficacy profiles of concurrent chemoradiotherapy (CCRT) with IMRT after durvalumab became clinically available. Methods: We reviewed the clinical records of patients with stage III non-small cell lung cancer (NSCLC) treated with CCRT and IMRT at seven centers in Japan and investigated relapse and survival from May 2018 to December 2019. The primary endpoint of this report was progression-free survival (PFS). Results: Among 107 patients enrolled in the study, 87 were sequentially administered durvalumab. From CCRT commencement, patients were followed up for a median period of 29.7 months. The median PFS at the end of the CCRT was 20.7 months. Among the 87 patients, 58 experienced disease relapses, of whom 36 (62.1 %) had distant metastases. Multivariate Cox regression analysis revealed that a favorable response to CCRT, a radiation dose ≥ 62 Gy, and stage IIIA NSCLC were associated with prolonged PFS (all P = 0.04). Multivariate logistic regression by landmark analysisHighlights: The tri-modalities of chemoradiotherapy (CRT) with IMRT and durvalumab were evaluated. We have reported the efficacy and safety of tri-modalities through real-world data. A better response to CRT and increasing radiation dose are related to long PFS. Durvalumab therapy duration was linked to survival in patients. Abstract: Purpose: Intensity-modulated radiotherapy (IMRT) is currently used more commonly than 3-dimensional conformal radiation for definitive thoracic radiation. We examined the efficacy profiles of concurrent chemoradiotherapy (CCRT) with IMRT after durvalumab became clinically available. Methods: We reviewed the clinical records of patients with stage III non-small cell lung cancer (NSCLC) treated with CCRT and IMRT at seven centers in Japan and investigated relapse and survival from May 2018 to December 2019. The primary endpoint of this report was progression-free survival (PFS). Results: Among 107 patients enrolled in the study, 87 were sequentially administered durvalumab. From CCRT commencement, patients were followed up for a median period of 29.7 months. The median PFS at the end of the CCRT was 20.7 months. Among the 87 patients, 58 experienced disease relapses, of whom 36 (62.1 %) had distant metastases. Multivariate Cox regression analysis revealed that a favorable response to CCRT, a radiation dose ≥ 62 Gy, and stage IIIA NSCLC were associated with prolonged PFS (all P = 0.04). Multivariate logistic regression by landmark analysis revealed that mortality risk factors were durvalumab treatment duration ≤ 11.7 months, a lower maximum grade of immune-related adverse events, FEV1 < 2805 mL, and radiation dose < 62 Gy (P = 0.01, 0.01, 0.03, and 0.04, respectively). Conclusions: In patients with NSCLC receiving CCRT using IMRT, long PFS was associated with a better response to CCRT, stage IIIA NSCLC, and an increased radiation dose. The duration of durvalumab consolidation also played an essential role in the survival of patients receiving CCRT with IMRT. (250 words) … (more)
- Is Part Of:
- Clinical and translational radiation oncology. Volume 37(2022)
- Journal:
- Clinical and translational radiation oncology
- Issue:
- Volume 37(2022)
- Issue Display:
- Volume 37, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 37
- Issue:
- 2022
- Issue Sort Value:
- 2022-0037-2022-0000
- Page Start:
- 57
- Page End:
- 63
- Publication Date:
- 2022-11
- Subjects:
- 3D-CRT 3-dimensional conformal radiation therapy -- 95% CI 95% confidence interval -- AE adverse event -- AIC Akaike's information criterion -- CCRT concurrent chemoradiotherapy -- FEV1 forced expiratory volume in 1 second -- HR hazard ratio -- OR odds ratio -- IMRT intensity-modulated radiotherapy -- IO immune-oncology -- irAE immune-related adverse event -- NSCLC non-small-cell lung cancer -- OS overall survival -- PFS progression-free survival -- PS performance status -- RECIST Response Evaluation Criteria in Solid Tumors -- ROC receiver operating characteristic
Concurrent chemoradiotherapy -- Durvalumab consolidation -- Intensity-modulated radiotherapy -- Landmark analysis -- Non-small cell lung cancer -- Multivariate analysis
Cancer -- Radiotherapy -- Periodicals
Oncology -- Periodicals
Cancer -- Radiotherapy
Oncology
Radiation Oncology
Neoplasms -- radiotherapy
Translational Medical Research
Periodicals
Electronic journals
Periodicals
616.9940642 - Journal URLs:
- https://www.journals.elsevier.com/clinical-and-translational-radiation-oncology ↗
http://www.sciencedirect.com/science/journal/24056308 ↗
http://www.sciencedirect.com/ ↗ - DOI:
- 10.1016/j.ctro.2022.08.010 ↗
- Languages:
- English
- ISSNs:
- 2405-6308
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- Legaldeposit
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