Survivorship program including long‐term toxicities and quality‐of‐life development over 10 years in a randomized trial in operable stage III non‐small‐cell lung cancer (ESPATUE)

Over 40% stage‐III non‐small‐cell lung cancer (NSCLC) patients (pts) experience 5‐year survival following multimodality treatment. Nevertheless, little is known about relevant late toxicities and quality‐of‐life (QoL) in the further long‐term follow‐up. Therefore, we invited pts from our randomized...

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Published inInternational journal of cancer Vol. 156; no. 1; pp. 154 - 163
Main Authors Schulte, Christina, Gauler, Thomas, Pöttgen, Christoph, Friedel, Godehard, Kopp, Hans‐Georg, Fischer, Berthold, Schmidberger, Heinz, Kimmich, Martin, Budach, Wilfried, Cordes, Sebastian, Wienker, Johannes, Metzenmacher, Martin, Los Rios, Rodrigo Hepp, Spengler, Werner, De Ruysscher, Dirk, Belka, Claus, Welter, Stefan, Luetke‐Brintrup, Diana, Guberina, Maja, Oezkan, Filiz, Darwiche, Kaid, Schuler, Martin, Jöckel, Karl‐Heinz, Aigner, Clemens, Stamatis, Georgios, Stuschke, Martin, Eberhardt, Wilfried Ernst Erich
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.01.2025
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Summary:Over 40% stage‐III non‐small‐cell lung cancer (NSCLC) patients (pts) experience 5‐year survival following multimodality treatment. Nevertheless, little is known about relevant late toxicities and quality‐of‐life (QoL) in the further long‐term follow‐up. Therefore, we invited pts from our randomized phase‐III trial (Eberhardt et al., Journal of Clinical Oncology 2015) after 10 years from diagnosis to participate within a structured survivorship program (SSP) including follow‐up imaging, laboratory parameters, cardio‐pulmonary investigations, long‐term toxicity evaluations and QoL questionnaires. Of 246 pts initially accrued, 161 were considered potentially resectable following the induction therapy and were randomized (80 to arm A: definitive chemoradiation; 81 to arm B: definitive surgery; 85 not randomized for different reasons; group C). 31 from 37 pts still alive after 10 years agreed to the SSP (13 in A; 12 in B; 6 in C). Clinically relevant long‐term toxicities (grade 3 and 4) were rarely observed with no signal favoring any of the randomization arms. Furthermore, available data from the global QoL analysis did not show a signal favoring any definitive locoregional approach (Mean QoL in SSP A pts: 56.41/100, B pts: 64.39/100) and no late decline in comparison to baseline and early 1‐year follow‐up. This is the first comprehensive SSP of very late survival follow‐up reported in stage‐III NSCLC treated within a randomized multimodality trial and it may serve as important baseline information for physicians and pts deciding for a locoregional treatment option. What's new? Long‐term survival of stage III non‐small cell lung cancer (NSCLC) has greatly improved, thanks largely to advances in multimodality treatment. Nonetheless, data on relevant late toxicities and quality‐of‐life following multimodality protocols are lacking. Here, the authors designed a structured survivorship program to investigate late‐stage toxicities and quality‐of‐life among stage III NSCLC patients treated in a randomized multimodality trial. Clinically relevant late‐stage grade 3 and 4 toxicities were found to be infrequent in the study population. Moreover, no significant differences were observed in quality‐of‐life between one‐ and 10‐year follow‐up. The observations potentially can inform decisions regarding multimodality treatment for advanced NSCLC.
Bibliography:Written on behalf of the ESPATUE/AIO (Arbeitsgemeinschaft Internistische Onkologie), ARO (Arbeitsgemeinschaft Radiologische Onkologie) and Clinical Trial Group of the German Cancer Society.
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ISSN:0020-7136
1097-0215
1097-0215
DOI:10.1002/ijc.35131