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Poster session 04

947P - Follow-up tests’ profitability in NSCLC: Experience of a tertiary hospital

Date

10 Sep 2022

Session

Poster session 04

Topics

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Virginia Calvo de Juan

Citation

Annals of Oncology (2022) 33 (suppl_7): S427-S437. 10.1016/annonc/annonc1062

Authors

V. Calvo de Juan1, F. Cano2, Y. Garitaonaindía Díaz1, A. Collazo Lorduy3, F.F. Franco4, M. Blanco Clemente1, M. Martinez Cutillas5, C. Traseira Puchol1, R. Aguado1, M. Provencio Pulla5

Author affiliations

  • 1 Medical Oncology Department, University Hospital Puerta de Hierro Majadahonda, 28222 - Majadahonda/ES
  • 2 Medical Oncology, University Hospital Puerta de Hierro Majadahonda, 28222 - Majadahonda/ES
  • 3 Medical Oncology, Centro Integral Oncologico Clara Campal, 28050 - Madrid/ES
  • 4 Medical Oncology, Hospital Puerta de Hierro-Majadahonda, 28222 - Madrid/ES
  • 5 Oncology Department, University Hospital Puerta de Hierro Majadahonda, 28222 - Majadahonda/ES

Resources

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Abstract 947P

Background

A significant portion of patients operated on for non-small cell lung cancer (NSCLC) will relapse eventually. There is currently no consensus regarding the best program for postoperative follow-up and surveillance after a curative resection of NSCLC patients. The objective of this study was to analyse the diagnostic capability of the diagnostic tests performed in our centre during the follow-up of patients with non-small cell lung cancer after surgical resection.

Methods

Retrospective review of 392 patients with surgically resected stage I-IIIA NSCLC. Data were collected for all patients treated between January 1, 2010 and December 31, 2020. We analysed clinical data, and recollected clinical, laboratory and radiological exams during their follow-up, identifying those that were relevant in the diagnosis of tumour relapses. We compared the monitoring carried out with the ESMO recommendations.

Results

67.1% of patients were male, with a median age of 66.0, and the most reported histology was adenocarcinoma (60.5). Median follow-up was 48.5 months. The data related to the follow-up tests performed and their diagnostic capability, as well as the expected number of tests carried out following ESMO recommendations are shown in the table. According to ESMO recommendations, we estimated that 1847 clinical revisions (mean 4.70) and 1847 Body CT (mean 4.70) should have been carried out. Table: 947P

Main evaluations performed and diagnostic yield

Routine Non routine
Total Mean Diagnostic of relapse % Total Mean Diagnostic of relapse %
Stage I Clinical revision 1029 5.33 2 0.19 15 0.08 15 100
Body CT 966 5.01 48 4.96 10 0.05 7 70
Stage II Clinical revision 473 5.44 3 0.63 7 0.08 7 100
Body CT 457 5.25 32 7 3 0.03 2 66.6
Stage IIIA Clinical revision 502 4.48 7 1.39 23 0.21 23 100
Body CT 482 4.30 48 9.96 13 0.05 9 69.2
Stages I-IIIA Clinical revision 2004 5.10 12 0.59 -
Body CT 1905 4.90 128 6.72

Conclusions

The vast majority of routine follow-up evaluations performed were not relevant for the management and only the body CT exceeded the threshold of 5% profitability, but without reaching 10% even in the highest stage. Profitability increased when they were carried out in a non-routine follow-up evaluation. The number of tests performed is similar to that expected following ESMO recommendations, which reinforces the clinical validity of the results. New follow-up strategies based on scientific evidence must be defined to improve the profitability of the tests performed.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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