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Surgical Treatment of Elderly Patients With cT1N0M0 Non-small Cell Lung Cancer Comparison Between Sublobar Resection and Lobectomy

Surgical Treatment of Elderly Patients With Early Stage Non-small Cell Lung Cancer (STEPS): Comparison Between Sublobar Resection and Lobectomy - an Open, Multicenter, Randomized Phase III Clinical Trial

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02360761
Acronym
STEPS
Enrollment
339
Registered
2015-02-11
Start date
2016-01-31
Completion date
2022-01-31
Last updated
2016-09-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-small Cell Lung Cancer

Keywords

Lung cancer;Elderly;Sublobar resection;Lobectomy

Brief summary

The role of sublobar resection(Wedge resection or anatomic segmentectomy) for small(≤ 2cm) early stage non-small cell lung cancer has been studied by Lung Cancer Study Group and is being studied by several ongoing trials. However, elderly patients(aged ≥70 years) in these trials is under-represented, as in most of the ongoing clinical trials. This study focuses on the elderly population of early stage lung cancer, and aims to investigate the outcome of lobectomy versus sublobar resection for peripheral stage I non-small cell lung cancer (NSCLC) in elderly patients.

Detailed description

This randomized trial is to the best of our knowledge the first one designed to compare sublobar resection and lobectomy for elderly patients, in order to address these open questions:In patients aged 70 years or older and with clinical stage T1N0M0 NSCLC, (1) whether sublobar resection can achieve similar disease-free survival compared to lobectomy, (2) whether sublobar resection can reduce the postoperative mortality and morbidity,(3) whether sublobar resection can reserve better pulmonary function and quality of life for elderly patients of NSCLC?

Interventions

PROCEDUREVATS

Patients undergo lobectomy,wedge resection, or anatomical segmentectomy by thoracoscopic surgery or video assisted thoracoscopic surgery.

PROCEDUREThoracotomy

Patients undergo lobectomy, wedge resection, or anatomic segmentectomy by thoracotomy.

Sponsors

Peking University People's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
70 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged 70 years or older * Preoperative criteria (contrast-enhanced Computed tomography scan) * Suspected non-small cell lung cancer * Clinical stage ⅠA, i.e. T1N0M0 (tumor diameter ≤3 cm, surrounded by visceral pleura, short-axis of lymph node \<1 cm or cold lymph nodes on PET scan) * The maximum diameter of consolidation of the maximum tumor diameter (consolidation/tumor ratio, C/T ratio) is no less than 0.5 in sub-solid lesions * Eligible for sublobar resection with sufficient margin * Intraoperative criteria * Histologically confirmed invasive NSCLC, i.e. NSCLC other than pre-invasive adenocarcinomas defined by The International Association for the Study of Lung Cancer (adenocarcinoma in situ, and minimally invasive adenocarcinoma) * Pathological exclusion of suspected lymph nodes involvement * Feasible to perform sublobar resection in terms of surgical margin requirement * General criteria * Must sign informed consent by the patient or his/her entrusted party * Must complete 4-year mortality index and comprehensive geriatric assessment(CGA) if necessary * The physiological reservation can tolerate lobectomy

Exclusion criteria

* Unable to comply with the study procedure * Past thoracic surgery history, except for diagnostic thoracoscopy * Malignant tumor history within the past 5 years, except for the following conditions: cured skin basal cell carcinoma, superficial bladder carcinoma, and uterine cervix cancer in situ * Any active systemic diseases including uncontrolled hypertension, unstable angina pectoris, newly onset of angina pectoris within recent 3 months, congestive heart failure (class II or plus of New York Heart Association, NYHA), myocardial infarction within recent 6 months, severe disease in the need of medication such as arrhythmia, liver, renal or metabolic diseases * Uncontrollable infections * Coexisting small cell lung cancer * Psychiatric diseases diagnosed * Other circumstances which is deemed inappropriate for enrollment by the researchers

Design outcomes

Primary

MeasureTime frameDescription
Time To Disease free survival Event3 yearsThe time interval from randomization to the earliest onset of any of the following events: tumor recurrence, metastasis, or death caused by any reason.

Secondary

MeasureTime frameDescription
Intubation time after surgery in Participants1 monthsDefined as the time interval from the day of operation to extubation.
Percentage of Participants With Local Recurrence and Metastasis Event3 yearsThe ratio of local recurrence and metastasis in 3 years from the day of randomization
Postoperative pulmonary function3 yearsThe Forced expiratory volume in one second and the forced vital capacity at 6-, 12- and 36-month post of the day of randomization.
Percentage of Participants With VATS procedure1 monthThe ratio of video assisted thoracoscopic surgery in each group.
Scores on the quality of life questionaires3 yearsThe scores of the 6-, 12- and 36-month questionaire on quality of life post of the day of randomization.
Percentage of Participants with Perioperative Complication and Death as a Measure of Safety.1 monthsPerioperative complication is defined as the complication occurred after surgery and before discharge, or within 30 days postoperatively. Death cases during this period should be recorded as perioperative death.
Hospitalization time after surgery in Participants1 monthsDefined as the time interval from the day of operation to discharge.
Time To Overall survival Event3 yearsThe time interval from randomization to death from any cause.

Other

MeasureTime frameDescription
The rate of pathologically noninvasive lung cancer with the radiologic character of C/T>0.51 monthThe radiologic character of C/T\>0.5 has been considered as a pathologically noninvasive lung cancer. and the rate of pathologically noninvasive lung cancer will be used as a measure for the relation between the radiologic / pathologic character of primary non-small-cell lung cancer and prognosis.
The morbidity rate as a measure between the two different interventions as a Measure of Safety and Tolerability.3 yearsThe morbidity rate after surgery for participants who underwent video-assisted thoracoscopic or open procedures a Measure of Safety and Tolerability.
The total cost as a measure of the cost/benefit analysis3 yearsThe cost/benefit analysis of sublobar resection versus lobectomy
The scores of CGA and 4-year mortality index as a measure of predictive factor for the outcome of the elderly.3 yearsThe scores of prospective CGA and 4-yr mortality index to predict the outcome of the elderly.

Countries

China

Contacts

Primary ContactJun Wang, M.M.
Jwangmd@yahoo.com+8601088326650
Backup ContactFan Yang, M.D.
+86010883266557

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026