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Long term follow-up of neoadjuvant chemotherapy for non-small cell lung cancer (NSCLC) investigating early positron emission tomography (PET) scan as a predictor of outcome

BACKGROUND: Neoadjuvant chemotherapy is effective in improving survival of resectable NSCLC. Based on findings in the adjuvant and metastatic setting, FDG positron emission tomography (PET) scans may offer early prognostic or predictive value after one cycle of induction chemotherapy. METHODS: In th...

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Autores principales: Romine, Perrin E., Martins, Renato G., Eaton, Keith D., Wood, Douglas E., Behnia, Fatemeh, Goulart, Bernardo H. L., Mulligan, Michael S., Wallace, Sarah G., Kell, Elizabeth, Bauman, Julie E., Patel, Shilpen A., Vesselle, Hubert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332837/
https://www.ncbi.nlm.nih.gov/pubmed/30642285
http://dx.doi.org/10.1186/s12885-019-5284-2
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author Romine, Perrin E.
Martins, Renato G.
Eaton, Keith D.
Wood, Douglas E.
Behnia, Fatemeh
Goulart, Bernardo H. L.
Mulligan, Michael S.
Wallace, Sarah G.
Kell, Elizabeth
Bauman, Julie E.
Patel, Shilpen A.
Vesselle, Hubert J.
author_facet Romine, Perrin E.
Martins, Renato G.
Eaton, Keith D.
Wood, Douglas E.
Behnia, Fatemeh
Goulart, Bernardo H. L.
Mulligan, Michael S.
Wallace, Sarah G.
Kell, Elizabeth
Bauman, Julie E.
Patel, Shilpen A.
Vesselle, Hubert J.
author_sort Romine, Perrin E.
collection PubMed
description BACKGROUND: Neoadjuvant chemotherapy is effective in improving survival of resectable NSCLC. Based on findings in the adjuvant and metastatic setting, FDG positron emission tomography (PET) scans may offer early prognostic or predictive value after one cycle of induction chemotherapy. METHODS: In this phase II non-randomized trial, patients with AJCC version 6 stage IB to IIIB operable NSCLC were treated with 3 cycles of cisplatin and pemetrexed neoadjuvant chemotherapy. Patients underwent FDG-PET scanning prior to and 18 to 21 days after the first cycle of chemotherapy. Investigators caring for patients were blinded to results, unless the scans showed evidence of disease progression. FDG-PET response was defined prospectively as a ≥ 20% decrease in the SUV of the primary lesion. RESULTS: Between October 2005 and February 2010, 25 patients enrolled. Fifty two percent were female, 88% white, and median age was 62 years. Histology was divided into adenocarcinoma 66%, not otherwise specified (NOS) 16%, squamous cell 12%, and large cell 4%. Stage distribution was: 16% IB, 4% IIB, and 79% IIIA. Treatment was well tolerated and only one patient had a grade 4 toxicity. The median follow up was 95 months. The 5 year progression free survival (PFS) and overall survival (OS) for the entire population were 54 and 67%, respectively. Eighteen patients had a baseline FDG-PET scan and a repeat scan at day 18–21 available for comparison. Ten patients (56%) were considered metabolic responders on the day 18–21 FDG-PET scan. Responders had a 5 year PFS and OS of 60 and 70%, respectively, while the percentage for non-responders was 63 and 75% (p = 0.96 and 0.85). CONCLUSIONS: This phase II trial did not demonstrate that a PET scan after one cycle of chemotherapy can predict survival outcomes of patients with NSCLC treated with neoadjuvant chemotherapy. TRIAL REGISTRATION: NCT00227539 registered September 28th, 2005.
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spelling pubmed-63328372019-01-23 Long term follow-up of neoadjuvant chemotherapy for non-small cell lung cancer (NSCLC) investigating early positron emission tomography (PET) scan as a predictor of outcome Romine, Perrin E. Martins, Renato G. Eaton, Keith D. Wood, Douglas E. Behnia, Fatemeh Goulart, Bernardo H. L. Mulligan, Michael S. Wallace, Sarah G. Kell, Elizabeth Bauman, Julie E. Patel, Shilpen A. Vesselle, Hubert J. BMC Cancer Research Article BACKGROUND: Neoadjuvant chemotherapy is effective in improving survival of resectable NSCLC. Based on findings in the adjuvant and metastatic setting, FDG positron emission tomography (PET) scans may offer early prognostic or predictive value after one cycle of induction chemotherapy. METHODS: In this phase II non-randomized trial, patients with AJCC version 6 stage IB to IIIB operable NSCLC were treated with 3 cycles of cisplatin and pemetrexed neoadjuvant chemotherapy. Patients underwent FDG-PET scanning prior to and 18 to 21 days after the first cycle of chemotherapy. Investigators caring for patients were blinded to results, unless the scans showed evidence of disease progression. FDG-PET response was defined prospectively as a ≥ 20% decrease in the SUV of the primary lesion. RESULTS: Between October 2005 and February 2010, 25 patients enrolled. Fifty two percent were female, 88% white, and median age was 62 years. Histology was divided into adenocarcinoma 66%, not otherwise specified (NOS) 16%, squamous cell 12%, and large cell 4%. Stage distribution was: 16% IB, 4% IIB, and 79% IIIA. Treatment was well tolerated and only one patient had a grade 4 toxicity. The median follow up was 95 months. The 5 year progression free survival (PFS) and overall survival (OS) for the entire population were 54 and 67%, respectively. Eighteen patients had a baseline FDG-PET scan and a repeat scan at day 18–21 available for comparison. Ten patients (56%) were considered metabolic responders on the day 18–21 FDG-PET scan. Responders had a 5 year PFS and OS of 60 and 70%, respectively, while the percentage for non-responders was 63 and 75% (p = 0.96 and 0.85). CONCLUSIONS: This phase II trial did not demonstrate that a PET scan after one cycle of chemotherapy can predict survival outcomes of patients with NSCLC treated with neoadjuvant chemotherapy. TRIAL REGISTRATION: NCT00227539 registered September 28th, 2005. BioMed Central 2019-01-14 /pmc/articles/PMC6332837/ /pubmed/30642285 http://dx.doi.org/10.1186/s12885-019-5284-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Romine, Perrin E.
Martins, Renato G.
Eaton, Keith D.
Wood, Douglas E.
Behnia, Fatemeh
Goulart, Bernardo H. L.
Mulligan, Michael S.
Wallace, Sarah G.
Kell, Elizabeth
Bauman, Julie E.
Patel, Shilpen A.
Vesselle, Hubert J.
Long term follow-up of neoadjuvant chemotherapy for non-small cell lung cancer (NSCLC) investigating early positron emission tomography (PET) scan as a predictor of outcome
title Long term follow-up of neoadjuvant chemotherapy for non-small cell lung cancer (NSCLC) investigating early positron emission tomography (PET) scan as a predictor of outcome
title_full Long term follow-up of neoadjuvant chemotherapy for non-small cell lung cancer (NSCLC) investigating early positron emission tomography (PET) scan as a predictor of outcome
title_fullStr Long term follow-up of neoadjuvant chemotherapy for non-small cell lung cancer (NSCLC) investigating early positron emission tomography (PET) scan as a predictor of outcome
title_full_unstemmed Long term follow-up of neoadjuvant chemotherapy for non-small cell lung cancer (NSCLC) investigating early positron emission tomography (PET) scan as a predictor of outcome
title_short Long term follow-up of neoadjuvant chemotherapy for non-small cell lung cancer (NSCLC) investigating early positron emission tomography (PET) scan as a predictor of outcome
title_sort long term follow-up of neoadjuvant chemotherapy for non-small cell lung cancer (nsclc) investigating early positron emission tomography (pet) scan as a predictor of outcome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332837/
https://www.ncbi.nlm.nih.gov/pubmed/30642285
http://dx.doi.org/10.1186/s12885-019-5284-2
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