Perioperative mortality and morbidity after sublobar versus lobar resection for early-stage non-small-cell lung cancer: Post-hoc analysis of an international, randomised, phase 3 trial (CALGB/Alliance 140503) Journal Article


Authors: Altorki, N. K.; Wang, X.; Wigle, D.; Gu, L.; Darling, G.; Ashrafi, A. S.; Landrenau, R.; Miller, D.; Liberman, M.; Jones, D. R.; Keenan, R.; Conti, M.; Wright, G.; Veit, L. J.; Ramalingam, S. S.; Kamel, M.; Pass, H. I.; Mitchell, J. D.; Stinchcombe, T.; Vokes, E.; Kohman, L. J.
Article Title: Perioperative mortality and morbidity after sublobar versus lobar resection for early-stage non-small-cell lung cancer: Post-hoc analysis of an international, randomised, phase 3 trial (CALGB/Alliance 140503)
Abstract: Background: Increased detection of small-sized, peripheral, non-small-cell lung cancer has renewed interest in sublobar resection instead of lobectomy, the traditional standard of care for early-stage lung cancer. We aimed to assess morbidity and mortality associated with lobar and sublobar resection for early-stage lung cancer. Methods: CALGB/Alliance 140503 is a multicentre, international, non-inferiority, phase 3 trial in patients with peripheral non-small-cell lung cancer clinically staged as T1aN0. Patients were recruited from 69 academic and community-based institutions in Australia, Canada, and the USA. Patients were randomly assigned intraoperatively to either lobar or sublobar resection. The random assignment was based on permuted block randomisation without concealment and was stratified according to radiographic tumour size, histology, and smoking status. The primary endpoint of the trial is disease-free survival; here, we report a post-hoc, exploratory, comparative analysis of perioperative mortality and morbidity associated with lobar and sublobar resection. Perioperative mortality was defined as death from any cause within 30 days and 90 days of surgical intervention and was calculated for all randomised patients. Morbidity was graded using Common Terminology Criteria for Adverse Events version 4.0. All analyses were done on an intention-to-treat basis for randomised patients with data available. This trial is registered with ClinicalTrials.gov, number NCT00499330. Findings: Between June 15, 2007, and March 13, 2017, 697 patients were randomly allocated to either lobar resection (n=357) or sublobar resection (n=340; 59% wedge resection). Six (0·9%) patients died by 30 days, four (1·1%) after lobar resection and two (0·6%) after sublobar resection; by 90 days, ten (1·4%) patients had died, six (1·7%) after lobar resection and four (1·2%) after sublobar resection (difference at 30 days, 0·5%, 95% CI −1·1 to 2·3; difference at 90 days, 0·5%, 95% CI −1·5 to 2·6). An adverse event of any grade occurred in 193 (54%) of 355 patients after lobar resection and 172 (51%) of 337 patients after sublobar resection. Adverse events of grade 3 or worse occurred in 54 (15%) patients assigned lobar resection and in 48 (14%) patients assigned sublobar resection. No differences between surgical approaches were noted in cardiac or pulmonary complications. Grade 3 haemorrhage (requiring transfusion) occurred in six (2%) patients assigned lobar resection and eight (2%) patients assigned sublobar resection. Prolonged air leak occurred in nine (3%) patients after lobar resection and two (1%) patients after sublobar resection. Interpretation: Our post-hoc analysis showed that perioperative mortality and morbidity did not seem to differ between lobar and sublobar resection in physically and functionally fit patients with clinical T1aN0 non-small-cell lung cancer. These data may affect the daily choices made by patients and their doctors in establishing the best treatment approach for stage I lung cancer. Funding: National Cancer Institute. © 2018 Elsevier Ltd
Keywords: adult; cancer survival; controlled study; treatment outcome; aged; major clinical study; hypertension; treatment duration; disease free survival; cancer staging; tumor volume; lung lobectomy; lung resection; morbidity; cancer mortality; coughing; dyspnea; pneumonia; hypoxia; postoperative complication; cause of death; confusion; hypotension; early cancer; pneumothorax; heart infarction; clinical evaluation; surgical infection; urinary tract infection; blood transfusion; postoperative infection; surgical mortality; intermethod comparison; colitis; atelectasis; pleura effusion; perioperative period; postoperative hemorrhage; postoperative pain; air leak; heart ventricle arrhythmia; heart muscle ischemia; adult respiratory distress syndrome; airway obstruction; non small cell lung cancer; post hoc analysis; randomized controlled trial (topic); postoperative thrombosis; lung complication; adverse event; pulmonary hypertension; heart supraventricular arrhythmia; septicemia; dysarthria; multicenter study (topic); sublobar resection; chylothorax; surgical injury; atrioventricular block; cardiopulmonary function; voice change; left ventricular diastolic dysfunction; respiratory tract fistula; faintness; human; male; female; priority journal; article; early cancer diagnosis; pulmonary aspiration; atrioventricular junction arrhythmia
Journal Title: The Lancet Respiratory Medicine
Volume: 6
Issue: 12
ISSN: 2213-2600
Publisher: Elsevier Inc.  
Date Published: 2018-12-01
Start Page: 915
End Page: 924
Language: English
DOI: 10.1016/s2213-2600(18)30411-9
PUBMED: 30442588
PROVIDER: scopus
PMCID: PMC6396275
DOI/URL:
Notes: Article -- Export Date: 1 February 2019 -- Source: Scopus
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  1. David Randolph Jones
    417 Jones