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1000 Titel
  • Planning target volume as a predictor of disease progression in inoperable stage III non-small cell lung cancer patients treated with chemoradiotherapy and concurrent and/or sequential immune checkpoint inhibition
1000 Autor/in
  1. Taugner, Julian |
  2. Käsmann, Lukas |
  3. Karin, Monika |
  4. Eze, Chukwuka |
  5. Flörsch, Benedikt |
  6. Guggenberger, Julian |
  7. Li, Minglun |
  8. Tufman, Amanda |
  9. Reinmuth, Niels |
  10. Duell, Thomas |
  11. Belka, Claus |
  12. Manapov, Farkhad |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-08-05
1000 Erschienen in
1000 Quellenangabe
  • 40(1):163-171
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s10637-021-01143-0 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8763767/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!The present study evaluates outcome after chemoradiotherapy (CRT) with concurrent and/or sequential Programmed Cell Death 1 (PD-1) or Ligand 1 (PD-L1) immune checkpoint inhibition (CPI) for inoperable stage III NSCLC patients depending on planning target volume (PTV).!##!Method and patients!#!Prospective data of thirty-three consecutive patients with inoperable stage III NSCLC treated with CRT and sequential durvalumab (67%, 22 patients) or concurrent and sequential nivolumab (33%, 11 patients) were analyzed. Different PTV cut offs and PTV as a continuous variable were evaluated for their association with progression-free (PFS), local-regional progression-free (LRPFS), extracranial distant metastasis-free (eMFS) and brain-metastasis free-survival (BMFS).!##!Results!#!All patients were treated with conventionally fractionated thoracic radiotherapy (TRT); 93% to a total dose of at least 60 Gy, 97% of patients received two cycles of concurrent platinum-based chemotherapy. Median follow-up for the entire cohort was 19.9 (range: 6.0-42.4) months; median overall survival (OS), LRFS, BMFS and eMFS were not reached. Median PFS was 22.8 (95% CI: 10.7-34.8) months. Patients with PTV ≥ 900ccm had a significantly shorter PFS (6.9 vs 22.8 months, p = 0.020) and eMFS (8.1 months vs. not reached, p = 0.003). Furthermore, patients with PTV ≥ 900ccm and stage IIIC disease (UICC-TNM Classification 8th Edition) achieved a very poor outcome with a median PFS and eMFS of 3.6 vs 22.8 months (p < 0.001) and 3.6 months vs. not reached (p = 0.001), respectively. PTV as a continuous variable also had a significant impact on eMFS (p = 0.048). However, no significant association of different PTV cut-offs or PTV as a continuous variable with LRPFS and BMFS could be shown. The multivariate analysis that was performed for PTV ≥ 900ccm and age (≥ 65 years), gender (male), histology (non-ACC) as well as T- and N-stage (T4, N3) as covariates also revealed PTV ≥ 900ccm as the only factor that had a significant correlation with PFS (HR: 5.383 (95% CI:1.263-22.942, p = 0.023)).!##!Conclusion!#!In this prospective analysis of inoperable stage III NSCLC patients treated with definitive CRT combined with concurrent and/or sequential CPI, significantly shorter PFS and eMFS were observed in patients with initial PTV ≥ 900ccm.
1000 Sacherschließung
lokal Age Factors [MeSH]
lokal Aged [MeSH]
lokal Antibodies, Monoclonal/therapeutic use [MeSH]
lokal Nivolumab/adverse effects [MeSH]
lokal Neoplasm Staging [MeSH]
lokal Male [MeSH]
lokal Antibodies, Monoclonal/administration
lokal Immune Checkpoint Inhibitors/adverse effects [MeSH]
lokal Immune Checkpoint Inhibitors/administration
lokal Chemoradiotherapy/adverse effects [MeSH]
lokal Sex Factors [MeSH]
lokal Short Report
lokal Carcinoma, Non-Small-Cell Lung/pathology [MeSH]
lokal Antineoplastic Agents, Immunological/adverse effects [MeSH]
lokal Female [MeSH]
lokal Lung Neoplasms/therapy [MeSH]
lokal Adult [MeSH]
lokal Humans [MeSH]
lokal Prospective Studies [MeSH]
lokal Tumor volume
lokal Chemoradiotherapy/methods [MeSH]
lokal Survival Analysis [MeSH]
lokal Checkpoint inhibition
lokal Middle Aged [MeSH]
lokal Prediction
lokal Immune Checkpoint Inhibitors/therapeutic use [MeSH]
lokal Chemoradiotherapy
lokal Non-small cell lung cancer
lokal Antineoplastic Agents, Immunological/therapeutic use [MeSH]
lokal Lung Neoplasms/pathology [MeSH]
lokal Nivolumab/administration
lokal Antineoplastic Agents, Immunological/administration
lokal Nivolumab/therapeutic use [MeSH]
lokal Antibodies, Monoclonal/adverse effects [MeSH]
lokal Carcinoma, Non-Small-Cell Lung/drug therapy [MeSH]
lokal Carcinoma, Non-Small-Cell Lung/therapy [MeSH]
lokal Lung Neoplasms/drug therapy [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/VGF1Z25lciwgSnVsaWFu|https://orcid.org/0000-0001-6260-5249|https://frl.publisso.de/adhoc/uri/S2FyaW4sIE1vbmlrYQ==|https://frl.publisso.de/adhoc/uri/RXplLCBDaHVrd3VrYQ==|https://frl.publisso.de/adhoc/uri/RmzDtnJzY2gsIEJlbmVkaWt0|https://frl.publisso.de/adhoc/uri/R3VnZ2VuYmVyZ2VyLCBKdWxpYW4=|https://frl.publisso.de/adhoc/uri/TGksIE1pbmdsdW4=|https://frl.publisso.de/adhoc/uri/VHVmbWFuLCBBbWFuZGE=|https://frl.publisso.de/adhoc/uri/UmVpbm11dGgsIE5pZWxz|https://frl.publisso.de/adhoc/uri/RHVlbGwsIFRob21hcw==|https://frl.publisso.de/adhoc/uri/QmVsa2EsIENsYXVz|https://frl.publisso.de/adhoc/uri/TWFuYXBvdiwgRmFya2hhZA==
1000 Hinweis
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1000 Erstellt am 2023-04-27T15:03:12.111+0200
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1000 Zuletzt bearbeitet 2023-10-20T14:24:23.173+0200
1000 Objekt bearb. Fri Oct 20 14:24:23 CEST 2023
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