Treatment and Survival in Advanced Non-Small Cell Lung Cancer, Urothelial, Ovarian, Gastric and Kidney Cancer: A Nationwide Comprehensive Evaluation.

Signe Sørup, Bianka Darvalics, Azza Ahmed Khalil, Marianne Nordsmark, Mette Hæe, Frede Donskov, Mads Agerbæk, Leo Russo, Dina Oksen, Emmanuelle Boutmy, Patrice Verpillat, Deirdre Cronin-Fenton
Author Information
  1. Signe Sørup: Department of Clinical Epidemiology, Department of Clinical Medicine, Aarhus University & Aarhus University Hospital, Aarhus, Denmark. ORCID
  2. Bianka Darvalics: Department of Clinical Epidemiology, Department of Clinical Medicine, Aarhus University & Aarhus University Hospital, Aarhus, Denmark. ORCID
  3. Azza Ahmed Khalil: Department of Oncology, Aarhus University Hospital, Aarhus, Denmark. ORCID
  4. Marianne Nordsmark: Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
  5. Mette Hæe: Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
  6. Frede Donskov: Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
  7. Mads Agerbæk: Department of Oncology, Aarhus University Hospital, Aarhus, Denmark. ORCID
  8. Leo Russo: Worldwide Medical and Safety, Pfizer, Collegeville, PA, USA.
  9. Dina Oksen: Global Epidemiology, Merck Healthcare KGaA, Darmstadt, Germany. ORCID
  10. Emmanuelle Boutmy: Global Epidemiology, Merck Healthcare KGaA, Darmstadt, Germany. ORCID
  11. Patrice Verpillat: Global Epidemiology, Merck Healthcare KGaA, Darmstadt, Germany. ORCID
  12. Deirdre Cronin-Fenton: Department of Clinical Epidemiology, Department of Clinical Medicine, Aarhus University & Aarhus University Hospital, Aarhus, Denmark. ORCID

Abstract

PURPOSE: Few studies have described real-world treatment patterns and survival before the widespread use of immune checkpoint inhibitors (ICIs). We aimed to describe anti-cancer treatment including the use of programmed cell death-1 and ligand-1 (PD-1/PD-L1) ICIs and overall survival (OS) in advanced cancer patients as a benchmarking real-world standard before widespread use of ICIs.
PATIENTS AND METHODS: Using nationwide Danish medical registries, we assembled cohorts of Danish patients with advanced non-small cell lung cancer (NSCLC) (n=12,283), urothelial carcinoma (n=2504), epithelial ovarian cancer (n=1466), gastric adenocarcinoma (n=1457), and renal cell carcinoma (RCC) (n=1261) diagnosed between 1/1/2013 and 31/12/2017. We describe anti-cancer treatment and OS using proportions, medians, and Kaplan-Meier methods.
RESULTS: Between 9% (ovarian cancer) and 25% (gastric adenocarcinoma) of patients did not receive anti-cancer treatment. The remaining patients received surgery, radiation therapy, and/or medical therapy. Chemotherapy was the most frequent medical therapy in all cohorts except for RCC (tyrosine kinase inhibitors). PD-L1/PD-1 ICIs were used in 7-8% of the NSCLC and RCC cohorts-mainly as second or higher line treatments. OS was longest in patients starting treatment with surgery (eg 25.6 months [95%-confidence interval (CI)=21.9-29.4] for NSCLC and 21.4 months [95%-CI=19.8-23.5] for urothelial carcinoma) and shortest for radiation therapy (eg 3.9 months [95%-CI=3.6-4.2] for NSCLC and 12.6 months [95%-CI=9.2-17.5] for urothelial carcinoma). NSCLC patients starting with medical therapy had OS between these limits. Median OS for NSCLC patients starting treatment with PD-L1/PD-1 ICIs was 21.4 months (95%-CI=13.9-not estimable).
CONCLUSION: Most patients with advanced NSCLC, urothelial carcinoma, epithelial ovarian cancer, gastric adenocarcinoma and RCC had poor OS in an era where only a minority received PD-L1/PD-1 ICIs. This information on treatment patterns and survival is important as a benchmarking real-world standard before widespread use of ICIs.

Keywords

References

  1. Clin Epidemiol. 2010 Aug 09;2:51-6 [PMID: 20865103]
  2. Int J Urol. 2019 Feb;26(2):202-210 [PMID: 30345560]
  3. Scand J Public Health. 2011 Jul;39(7 Suppl):42-5 [PMID: 21775350]
  4. Cancer Chemother Pharmacol. 2019 Aug;84(2):227-240 [PMID: 31240384]
  5. J Chronic Dis. 1987;40(5):373-83 [PMID: 3558716]
  6. Clin Epidemiol. 2019 Jul 12;11:563-591 [PMID: 31372058]
  7. Nat Rev Drug Discov. 2018 Nov 28;17(12):854-855 [PMID: 30482962]
  8. Transl Lung Cancer Res. 2019 Sep;8(Suppl 2):S192-S201 [PMID: 31673524]
  9. Ann Oncol. 2016 Jan;27(1):159-65 [PMID: 26489444]
  10. Ann Oncol. 2016 Sep;27(suppl 5):v58-v68 [PMID: 27664262]
  11. Epidemiology. 2020 Jul;31(4):599-603 [PMID: 32483069]
  12. Hum Vaccin Immunother. 2019;15(5):1111-1122 [PMID: 30888929]
  13. Int J Qual Health Care. 2019 Nov 30;31(9):717-720 [PMID: 31220255]
  14. J Gastrointest Cancer. 2019 Dec;50(4):780-793 [PMID: 30078125]
  15. Oncologist. 2019 Jan;24(1):103-109 [PMID: 30120163]
  16. Expert Rev Anticancer Ther. 2017 May;17(5):427-437 [PMID: 28277806]
  17. BMC Cancer. 2019 Jun 7;19(1):548 [PMID: 31174493]
  18. Scand J Public Health. 2011 Jul;39(7 Suppl):72-4 [PMID: 21775357]
  19. Cancer Treat Res Commun. 2020;25:100266 [PMID: 33316557]
  20. Transl Lung Cancer Res. 2019 Jun;8(3):202-207 [PMID: 31367533]
  21. Gastric Cancer. 2020 Jul;23(4):565-578 [PMID: 32468420]
  22. Future Oncol. 2019 Oct;15(30):3491-3502 [PMID: 31497994]
  23. Clin Epidemiol. 2013 Aug 30;5:327-34 [PMID: 24039450]
  24. Clin Epidemiol. 2015 Nov 17;7:449-90 [PMID: 26604824]
  25. Eur J Epidemiol. 2014 Aug;29(8):541-9 [PMID: 24965263]
  26. Expert Opin Biol Ther. 2019 Dec;19(12):1265-1274 [PMID: 31518156]
  27. N Engl J Med. 2018 Jan 11;378(2):158-168 [PMID: 29320654]
  28. J Oncol Pract. 2013 Jan;9(1):20-6 [PMID: 23633967]
  29. Clin Epidemiol. 2012;4 Suppl 2:39-44 [PMID: 22936855]
  30. Ann Oncol. 2014 Sep;25 Suppl 3:iii27-39 [PMID: 25115305]
  31. Epidemiology. 2018 May;29(3):442-447 [PMID: 29337844]

Word Cloud

Created with Highcharts 10.0.0treatmentpatientsICIsNSCLCOScancercellcarcinomatherapymonthssurvivaluseinhibitorsmedicalurothelialRCCreal-worldwidespreadimmunecheckpointanti-cancerprogrammedadvancedovariangastricadenocarcinomaPD-L1/PD-1startingpatternsdescribedeath-1benchmarkingstandardDanishcohortsepithelialreceivedsurgeryradiationeg62145]PURPOSE:studiesdescribedaimedincludingligand-1PD-1/PD-L1overallPATIENTSANDMETHODS:Usingnationwideregistriesassemblednon-smalllungn=12283n=2504n=1466n=1457renaln=1261diagnosed1/1/201331/12/2017usingproportionsmediansKaplan-MeiermethodsRESULTS:9%25%receiveremainingand/orChemotherapyfrequentexcepttyrosinekinaseused7-8%cohorts-mainlysecondhigherlinetreatmentslongest25[95%-confidenceintervalCI=219-294][95%-CI=198-23shortest39[95%-CI=36-42]12[95%-CI=92-17limitsMedian95%-CI=139-notestimableCONCLUSION:pooreraminorityinformationimportantTreatmentSurvivalAdvancedNon-SmallCellLungCancerUrothelialOvarianGastricKidneyCancer:NationwideComprehensiveEvaluationimmunotherapydeath-ligand-1

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