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Randomized controlled trials in lung cancer surgery: How are we doing?
Wong, Lye-Yeng; Li, Yanli; Elliott, Irmina A; Backhus, Leah M; Berry, Mark F; Shrager, Joseph B; Oh, Daniel S.
Afiliación
  • Wong LY; Department of Cardiothoracic Surgery, Stanford University Medical Center, Stanford, Calif.
  • Li Y; Department of Medical Affairs, Intuitive Surgical, Sunnyvale, Calif.
  • Elliott IA; Department of Cardiothoracic Surgery, Stanford University Medical Center, Stanford, Calif.
  • Backhus LM; VA Palo Alto Health Care System, Palo Alto, Calif.
  • Berry MF; Department of Cardiothoracic Surgery, Stanford University Medical Center, Stanford, Calif.
  • Shrager JB; VA Palo Alto Health Care System, Palo Alto, Calif.
  • Oh DS; Department of Cardiothoracic Surgery, Stanford University Medical Center, Stanford, Calif.
JTCVS Open ; 18: 234-252, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38690441
ABSTRACT

Objective:

Randomized control trials are considered the highest level of evidence, yet the scalability and practicality of implementing randomized control trials in the thoracic surgical oncology space are not well described. The aim of this study is to understand what types of randomized control trials have been conducted in thoracic surgical oncology and ascertain their success rate in completing them as originally planned.

Methods:

The ClinicalTrials.gov database was queried in April 2023 to identify registered randomized control trials performed in patients with lung cancer who underwent surgery (by any technique) as part of their treatment.

Results:

There were 68 eligible randomized control trials; 33 (48.5%) were intended to examine different perioperative patient management strategies (eg, analgesia, ventilation, drainage) or to examine different intraoperative technical aspects (eg, stapling, number of ports, port placement, ligation). The number of randomized control trials was relatively stable over time until a large increase in randomized control trials starting in 2016. Forty-four of the randomized control trials (64.7%) were open-label studies, 43 (63.2%) were conducted in a single facility, 66 (97.1%) had 2 arms, and the mean number of patients enrolled per randomized control trial was 236 (SD, 187). Of 21 completed randomized control trials (31%), the average time to complete accrual was 1605 days (4.4 years) and average time to complete primary/secondary outcomes and adverse events collection was 2125 days (5.82 years).

Conclusions:

Given the immense investment of resources that randomized control trials require, these findings suggest the need to scrutinize future randomized control trial proposals to assess the likelihood of successful completion. Future study is needed to understand the various contributing factors to randomized control trial success or failure.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: JTCVS Open Año: 2024 Tipo del documento: Article Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: JTCVS Open Año: 2024 Tipo del documento: Article Pais de publicación: Países Bajos