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Time to treatment initiation and its impact on real-world survival in metastatic colorectal cancer and pancreatic cancer.
Gbolahan, Olumide; Hashemi-Sadraei, Neda; Yash, Suri; Williams, Grant; Ramachandran, Rekha; Kim, Young-Il; Paluri, Ravikumar; Outlaw, Darryl; El-Rayes, Bassel; Nabell, Lisle.
Affiliation
  • Gbolahan O; Birmingham School of Medicine and O'Neal Comprehensive Cancer Center, University of Alabama, Birmingham, Alabama, USA.
  • Hashemi-Sadraei N; University of New Mexico School of Medicine, New Mexico, USA.
  • Yash S; Birmingham School of Medicine and O'Neal Comprehensive Cancer Center, University of Alabama, Birmingham, Alabama, USA.
  • Williams G; Birmingham School of Medicine and O'Neal Comprehensive Cancer Center, University of Alabama, Birmingham, Alabama, USA.
  • Ramachandran R; Division of Preventive Medicine, University of Alabama School of Medicine, Birmingham, Alabama, USA.
  • Kim YI; Division of Preventive Medicine, University of Alabama School of Medicine, Birmingham, Alabama, USA.
  • Paluri R; Birmingham School of Medicine and O'Neal Comprehensive Cancer Center, University of Alabama, Birmingham, Alabama, USA.
  • Outlaw D; Wake Forest School of Medicine, North Carolina, United States.
  • El-Rayes B; Birmingham School of Medicine and O'Neal Comprehensive Cancer Center, University of Alabama, Birmingham, Alabama, USA.
  • Nabell L; Emory University School of Medicine, and Winship Cancer Institute, Georgia.
Cancer Med ; 12(3): 3488-3498, 2023 02.
Article in En | MEDLINE | ID: mdl-35979540
ABSTRACT

BACKGROUND:

Given the dearth of data regarding the time to treatment initiation (TTI) in the palliative setting, and its impact on survival outcomes, we sought to determine TTI in a real-world cohort of metastatic colorectal cancer (mCRC) and metastatic pancreatic cancer (mPC) patients and evaluate the impact of TTI on real-world survival outcomes.

METHODS:

We collected survival and treatment data for mCRC and mPC from the Flatiron Health electronic health records (EHR) derived database. We divided TTI into 3 categories < 2 weeks, 2-< 4 weeks, and 4-8 weeks, from diagnosis to first-line therapy. Outcome measures were median TTI, real-world overall survival (RW-OS) based on TTI categories by Kaplan-Meier method, and impact of TTI on survival using cox proportional hazard models.

RESULTS:

Among 7108 and 3231 patients with mCRC and mPC treated within 8 weeks of diagnosis, the median TTI were 28 days and 20 days. Median RW-OS for mCRC was 24 months; 26.9 months versus 22.6 and 18.05 months in the 4-8-week, 2-< 4 week (control) and < 2-week groups, respectively (p < 0.0001). For mPC, median RW-OS was 8 months, without significant difference in RW-OS among the groups (p = 0.05). The 4-8-week group was associated with lower hazard of death (HR 0.782, 95% CI 0.73-0.84, p < 0.0001) and the < 2-week group was associated with a higher hazard of death (HR 1.26, 95% CI 1.15-1.38, p < 0.0001) in mCRC. The 4-8-week group was associated with lower hazard of death for mPC (HR 0.88, 95% CI 0.8-0.97, p = 0.0094).

CONCLUSION:

In a real-world cohort of patients treated within 8 weeks of diagnosis, and with the limitations of a retrospective study, later TTI did not have a negative impact on survival outcomes in mCRC and mPC.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancreatic Neoplasms / Rectal Neoplasms / Colorectal Neoplasms / Colonic Neoplasms Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Cancer Med Year: 2023 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancreatic Neoplasms / Rectal Neoplasms / Colorectal Neoplasms / Colonic Neoplasms Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Cancer Med Year: 2023 Type: Article Affiliation country: United States