Recurrence of Non-Small Cell Lung Cancer With Visceral Pleural Invasion: A Seconday Analysis of a Randomized Clinical Trial.


Journal

JAMA oncology
ISSN: 2374-2445
Titre abrégé: JAMA Oncol
Pays: United States
ID NLM: 101652861

Informations de publication

Date de publication:
01 Aug 2024
Historique:
medline: 1 8 2024
pubmed: 1 8 2024
entrez: 1 8 2024
Statut: aheadofprint

Résumé

The randomized clinical trial Cancer and Leukemia Group B (CALGB) 140503 showed that for patients with clinically staged T1N0 non-small cell lung cancer (NSCLC; ≤2 cm), sublobar resections were associated with similar oncological outcomes to those after lobar resection. The association of the extent of parenchymal resection with recurrence and survival in patients with tumors pathologically upstaged to T2 based on visceral pleural invasion (VPI) is controversial. To determine survival and recurrence rates in patients with small peripheral pT2 NSCLC (≤2 cm) that was treated by either lobar or sublobar resection in CALGB 140503. CALGB 140503, a randomized multicenter noninferiority trial, included 697 patients with small peripheral NSCLC that was clinically staged as T1N0. Enrollment was from June 2007 through March 2017 at 83 participating institutions, and after a median follow-up of 7 years, the primary outcome of disease-free survival after sublobar resection was noninferior to that after lobar resection. Lobar or sublobar resection. Survival end points were estimated by the Kaplan-Meier estimator. Hazard ratios and 95% CIs were estimated using stratified Cox proportional hazard models. Of 679 participants, 390 (57.4%) were female, and the median (range) age was 67.8 (37.8-89.7) years. Among 697 patients randomized, 566 (81.2%) had pT1 tumors (no VPI) and 113 (16.2%) had pT2 tumors (VPI). Five-year disease-free survival was 65.9% (95% CI, 61.9%-70.2%) in patients with pT1 compared with 53.3% (95% CI, 44.3%-64.1%) in patients with pT2 tumors (stratified log-rank: P = .02). Disease recurrence developed in 27.6% of patients with pT1 (locoregional only: 60 [10.8%]; distant only: 81 [14.6%]) and 41.6% of those with pT2 (locoregional only: 17 [15.0%]; distant only: 27 [23.9%]). Five-year recurrence-free survival was 73.1% (95% CI, 69.2%-77.1%) for pT1 tumors and 58.2% (95% CI, 49.2%-68.8%) for pT2 tumors (stratified log-rank: P = .01). There were no intergroup differences in disease-free or recurrence-free survival based on the extent of parenchymal resection. The results of this secondary analysis suggest that compared with patients with tumors without VPI, patients who had tumors with VPI had worse disease-free and recurrence-free survival and a higher rate of local and distant disease recurrence. These high rates of recurrence were independent of the extent of parenchymal resection, and these data support the inclusion of these patients in adjuvant therapy trials. ClinicalTrials.gov Identifier: NCT0049933.

Identifiants

pubmed: 39088196
pii: 2821929
doi: 10.1001/jamaoncol.2024.2491
doi:

Banques de données

ClinicalTrials.gov
['NCT00049933']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Nasser Altorki (N)

Weill Cornell Medicine, New York-Presbyterian Hospital, New York.

Xiaofei Wang (X)

Alliance Statistics and Data Management Center, and Biostatistics and Bioinformatics, Duke University, Durham, North Carolina.

Bryce Damman (B)

Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, Minnesota.

David R Jones (DR)

Memorial Sloan Kettering Cancer Center, New York, New York.

Dennis Wigle (D)

Mayo Clinic, Rochester, Minnesota.

Jeffrey Port (J)

Weill Cornell Medicine, New York-Presbyterian Hospital, New York.

Massimo Conti (M)

Institut Universitaire de Cardiologie et Pneumologie de Québec, Quebec , Canada.

Ahmad S Ashrafi (AS)

Surrey Memorial Hospital Thoracic Group Fraser Valley Health Authority, British Columbia, Canada.

Moishe Lieberman (M)

Centre Hospitalier de l'Université de Montréal, Montreal, Québec, Canada.

Rodney Landreneau (R)

Tampa General Hospital, Tampa, Florida.

Kazuhiro Yasufuku (K)

University of Toronto, Toronto, Ontario, Canada.

Stephen Yang (S)

Johns Hopkins University, Baltimore, Maryland.

John D Mitchell (JD)

University of Colorado Hospital School of Medicine, Aurora.

Robert Keenan (R)

Moffitt Cancer Center, Tampa, Florida.

Thomas Bauer (T)

Hackensack Meridian Health System, Edison, New Jersey.

Daniel Miller (D)

Medical College of Georgia, Augusta.

David Kozono (D)

Alliance Protocol Operations Office, Boston, Massachusetts.

Jennifer Mentlick (J)

Alliance Statistics and Data Management Center, Mayo Clinic, Rochester, Minnesota.

Everett Vokes (E)

University of Chicago Comprehensive Cancer Center, Chicago, Illinois.

Thomas E Stinchcombe (TE)

Duke Cancer Institute, Duke University Medical Center, Durham, North Carolina.

Classifications MeSH