Tumor Growth Rate (TGR) Predicts Clinical Outcomes for Advanced Non-small Cell Lung Cancer Undergoing Immunotherapy.

Sponsor
Sun Yat-sen University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04722406
Collaborator
Guangdong Provincial Hospital of Traditional Chinese Medicine (Other), Shanghai Chest Hospital (Other)
350
3
23.6
116.7
5

Study Details

Study Description

Brief Summary

We hypothesized that TGR could serve as an early predictor of outcomes for aNSCLC patients undergoing immune checkpoint inhibitors (ICIs). A retrospective analysis was conducted to investigate the association of TGR with response and long-term survival of aNSCLC patients undergoing ICI therapy.

Condition or Disease Intervention/Treatment Phase
  • Other: This item is not applicable to our observational study.

Detailed Description

Tumor growth rate (TGR) signifies percentage change in tumor size per month (%/m). Electronic medical records were retrospectively reviewed for all histologically confirmed aNSCLC patients undergoing anti-PD-1/PD-L1 therapy at Sun Yat-Sen University Cancer Center (SYSUCC) between August 2016 and June 2018.

All response and outcome evaluation were determined as per RECIST 1.1 by two senior radiologists blinded to patients'information. Discrepancy was solved by consensus.

X-tile software was used to determine cut-off values that maximumly differentiate overall survival (OS). Log-rank tests and Cox regression models were performed for survival analysis. The predictive value of TGR for clinical outcomes in ICI-treated aNSCLC patients was validated in two external cohorts, recruited form Guangdong Province Traditional Chinese Medical Hospital and Shanghai Chest Hospital.

Study Design

Study Type:
Observational
Anticipated Enrollment :
350 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Tumor Growth Rate (TGR) as an Early Predictor of Clinical Outcomes in Advanced Non-small Cell Lung Cancer Treated With PD-1 Axis Inhibitors.
Actual Study Start Date :
Aug 15, 2019
Anticipated Primary Completion Date :
Jul 1, 2021
Anticipated Study Completion Date :
Aug 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Low TGR group

Patients with low level of TGR determined by X-tile program

Other: This item is not applicable to our observational study.
This item is not applicable to our observational study.

High TGR group

Patients with high level of TGR determined by X-tile program

Other: This item is not applicable to our observational study.
This item is not applicable to our observational study.

Outcome Measures

Primary Outcome Measures

  1. Overall survival of patients undergoing ICI monotherapy [From date of ICI treatment initiation until the date of death from any causes, assessed up to 100 months.]

    Overall survival (OS) was defined as the time from immunotherapy initiation to death from any causes.

Secondary Outcome Measures

  1. Progression-free survival of patients undergoing ICI monotherapy. [From date of ICI treatment initiation until the date of first documented progression or date of death from any causes, whichever came first, assessed up to 100 months.]

    Progression-free survival was calculated from ICI initiation to radiologically-defined progression or death from any causes.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Histologically confirmed aNSCLC patients

  • Having received anti-PD-1/PD-L1 therapy

  • Must have two consecutive computed tomography (CT) scans upon early treatment (from baseline to the first imaging evaluation)

Exclusion Criteria:
  • Lacking available computed tomography (CT) evaluation at any of two time points-baseline and the first evaluation

  • Without measurable lesions at baseline CT scan

  • Having received local anticancer therapy during ICI treatment, for example, radiotherapy and radiofrequency ablation

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sun Yat-sen University Cancer Center Guangzhou Guangdong China 510060
2 Guangdong Provincial Hospital of Traditional Chinese Medicine Guangzhou Guangdong China 510120
3 Shaihai Chest Hospital Shanghai Shanghai China 200030

Sponsors and Collaborators

  • Sun Yat-sen University
  • Guangdong Provincial Hospital of Traditional Chinese Medicine
  • Shanghai Chest Hospital

Investigators

  • Principal Investigator: Shaodong Hong, MD, Sun Yat-sen University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Shaodong Hong, Deputy Chief Physician, MD, Sun Yat-sen University
ClinicalTrials.gov Identifier:
NCT04722406
Other Study ID Numbers:
  • SHong
First Posted:
Jan 25, 2021
Last Update Posted:
Mar 17, 2021
Last Verified:
Mar 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Shaodong Hong, Deputy Chief Physician, MD, Sun Yat-sen University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 17, 2021