Mapping the patient journey and treatment patterns in early-stage (stage I-III) non-small cell lung cancer.

Diagnosis pathway Early-stage NSCLC

Journal

Cancer epidemiology
ISSN: 1877-783X
Titre abrégé: Cancer Epidemiol
Pays: Netherlands
ID NLM: 101508793

Informations de publication

Date de publication:
01 Oct 2024
Historique:
received: 13 06 2024
revised: 17 08 2024
accepted: 15 09 2024
medline: 3 10 2024
pubmed: 3 10 2024
entrez: 2 10 2024
Statut: aheadofprint

Résumé

We map the patient journey from symptom onset to intervention and describe primary treatment in a retrospective population-based cohort study of patients in a large healthcare-provider. Newly diagnosed adult patients diagnosed with stages I-III non-small cell lung cancer (NSCLC) between 2016 and 2019 were identified from the Israel National Cancer Registry and chart review was performed to extract de-identified data. The following timelines were constructed: from symptom onset to imaging, imaging to biopsy, and biopsy to primary treatment initiation. Cutoff: 31st December 2021. The initial symptom was captured up to one year prior to biopsy. Among 302 patients (41 % female, 70 % >=65 years, 79 % former or current smoking, 62 % adenocarcinoma), 34.1 % stage I, 10.3 % stage II, 42.1 % stage III and 13.6 % unknown (AJCC ver. 8). In the baseline year, 80.5 % of patients reported at least one symptom to their physician, and 12.3 % reported four or more symptoms. The most common symptoms reported were cough (29.8 %), pneumonia (24.2 %), chest pain (18.5 %), bronchitis (17.5 %) and wheezing (17.2 %). For patients with an initial symptom (n=243) median time from symptom onset to imaging was 5.5 months (95% CI:4.8-6.3), and time from imaging to primary treatment initiation was 2.6 (2.3-2.9) months in all patients. Total duration from symptom to intervention was 8.5 months (7.6-9.3). Over 93 % of stage I patients underwent surgery and 4.9 % received definitive radiation. Over 83 % of stage II patients underwent surgery; of these, 54.8 % received adjuvant/neoadjuvant chemotherapy. Of stage III patients, 68.5 % received definitive chemoradiation (half received durvalumab), and the remaining underwent surgery with adjuvant/neoadjuvant treatment. A total of 80.5 % of patients were symptomatic and the median duration from symptom onset to treatment initiation was 8.5 month long. Improving patient and physician awareness to lung cancer symptoms, and the introduction of screening programs are essential for reducing those delays.

Identifiants

pubmed: 39357215
pii: S1877-7821(24)00157-7
doi: 10.1016/j.canep.2024.102678
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

102678

Informations de copyright

Copyright © 2024 Moser. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest This work was supported by Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA. Maccabi and MSD wrote the protocol. Maccabi submitted IRB approval, developed the analytic data set, wrote the statistical analysis plan, performed all analyses and wrote the final report. MSD and Maccabi reviewed the preliminary and final results, and are co-authors of this manuscript. SSM, LA, GC, SG, NSD have no conflict of interest. SY is an employee of MSD Ltd., Hod Hasharon, Israel and own stocks in Merck & Co., Inc., Rahway, NJ, USA. BP and MvR are employees of MSD, AA is an employee of Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA, and all own stocks in Merck & Co., Inc., Rahway, NJ, USA.

Auteurs

Sarah Sharman Moser (S)

Maccabi Institute for Research and Innovation (Maccabitech), Maccabi Healthcare Services, HaMered 27, Tel Aviv, 68125, Israel. Electronic address: moser_sa@mac.org.il.

Shira Yaari (S)

MSD Israel, 34 Hacharash St. P.O.B 7340; Neve Neeman B; Hod Hasharon, 45240, Israel.

Lior Apter (L)

Health Division, Maccabi Healthcare Services, HaMered 27, Tel Aviv, 68125, Israel; Department of Health Systems, Ben-Gurion University of the Negev, Beer-Sheva, Israel.

Bernadette Poellinger (B)

MSD Sharp & Dohme, GmbH, Germany.

Milan Rheenen (M)

MSD B.V., Haarlem, the Netherlands.

Ashwini Arunachalam (A)

Merck & Co., Inc., Rahway, NJ, USA.

Gabriel Chodick (G)

Maccabi Institute for Research and Innovation (Maccabitech), Maccabi Healthcare Services, HaMered 27, Tel Aviv, 68125, Israel; Faculty of Medicine, Tel Aviv University, Israel.

Moshe Hoshen (M)

Maccabi Institute for Research and Innovation (Maccabitech), Maccabi Healthcare Services, HaMered 27, Tel Aviv, 68125, Israel.

Sivan Gazit (S)

Maccabi Institute for Research and Innovation (Maccabitech), Maccabi Healthcare Services, HaMered 27, Tel Aviv, 68125, Israel.

Nava Siegelmann-Danieli (N)

Health Division, Maccabi Healthcare Services, HaMered 27, Tel Aviv, 68125, Israel; Faculty of Medicine, Tel Aviv University, Israel.

Classifications MeSH