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Trial · NCT04647110

Outcomes27

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
SECONDARYDuration of Treatment: Based on Treatment Cohort GroupsFrom index date to treatment completion/discontinuation during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Here, Overall Number of Participants Analyzed signifies participants who were evaluable for this outcome measure based on generation of ALK treatment.
YearsMEAN
SECONDARYDuration of Treatment: Based on Chemotherapy StatusFrom index date to treatment completion/discontinuation during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed.YearsMEAN
SECONDARYDuration of Treatment: Based on ALK Sequencing, 1 Line of ALK TKI TreatmentFrom index date to treatment completion/discontinuation during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Here, Overall Number of Participants Analyzed (N) signifies participants evaluable for this measure and received only 1 line of ALK TKIs with/ without chemotherapy. Due to ethical compliance, it was pre-planned not to report data for those reporting groups which had \<5 participants at the index date.
YearsMEAN
SECONDARYDuration of Treatment: Based on ALK Sequencing, 2 Lines of ALK TKI TreatmentFrom index date to treatment completion/discontinuation during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Overall Number of Participants Analyzed (N): participants evaluable for this measure and received only 2 lines of ALK TKIs with/ without chemotherapy. Groups with N =0: no participants with respective ALK TKI sequencing. Due to ethical compliance, it was pre-planned not to report data for those reporting groups which had \<5 participants at the index date.
YearsMEAN
SECONDARYDuration of Treatment: Based on ALK Sequencing, 3 Lines of ALK TKI TreatmentFrom index date to treatment completion/discontinuation during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Overall Number of Participants Analyzed (N): participants evaluable for this measure and received only 3 lines of ALK TKIs with/ without chemotherapy. Groups with N =0: no participants with respective ALK TKI sequencing. Due to ethical compliance, it was pre-planned not to report data for those reporting groups which had \<5 participants at the index date.
YearsMEAN
SECONDARYDuration of Treatment: Based on ALK Sequencing, More Than or Equal to (>=) 4 Lines of ALK TKI TreatmentFrom index date to treatment completion/discontinuation during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Here, Overall Number of Participants Analyzed signifies participants who were evaluable for this outcome measure and received \>= 4 lines of ALK TKI treatment with or without chemotherapy.
YearsMEAN
PRIMARYOverall Survival (OS): Based on Treatment Cohort GroupsFrom index date to the date of death due to any cause or censoring date, during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Here, Overall Number of Participants Analyzed signifies participants who were evaluable for this outcome measure based on generation of ALK treatment.
YearsMEDIAN
PRIMARYOverall Survival: Based on Chemotherapy StatusFrom index date to the date of death due to any cause or censoring date, during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed.YearsMEDIAN
PRIMARYOverall Survival: Based on Central Nervous System (CNS) Metastases StatusFrom index date to the date of death due to any cause or censoring date, during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed.YearsMEDIAN
PRIMARYOverall Survival: Based on ALK Sequencing, 1 Line of ALK TKI TreatmentFrom index date to the date of death due to any cause or censoring date, during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Here, Overall Number of Participants Analyzed (N) signifies participants evaluable for this measure and received only 1 line of ALK TKIs with/ without chemotherapy. Due to ethical compliance, it was pre-planned not to report data for those reporting groups which had \<5 participants at the index date.
YearsMEDIAN
PRIMARYOverall Survival: Based on ALK Sequencing, 2 Lines of ALK TKI TreatmentFrom index date to the date of death due to any cause or censoring date, during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Overall Number of Participants Analyzed (N): participants evaluable for this measure and received only 2 lines of ALK TKIs with/ without chemotherapy. Groups with N =0: no participants with respective ALK TKI sequencing. Due to ethical compliance, it was pre-planned not to report data for those reporting groups which had \<5 participants at the index date.
YearsMEDIAN
PRIMARYOverall Survival: Based on ALK Sequencing, 3 Lines of ALK TKI TreatmentFrom index date to the date of death due to any cause or censoring date, during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Overall Number of Participants Analyzed (N): participants evaluable for this measure and received only 3 lines of ALK TKIs with/ without chemotherapy. Groups with N =0: no participants with respective ALK TKI sequencing. Due to ethical compliance, it was pre-planned not to report data for those reporting groups which had \<5 participants at the index date.
YearsMEDIAN
PRIMARYOverall Survival: Based on ALK Sequencing, More Than or Equal to (>=) 4 Lines of ALK TKI TreatmentFrom index date to the date of death due to any cause or censoring date, during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Here, Overall Number of Participants Analyzed signifies participants who were evaluable for this outcome measure and received \>= 4 lines of ALK TKI treatment with or without chemotherapy.
YearsMEDIAN
PRIMARYPercentage of Participants Alive After 5 Years From Index Date: Based on Treatment Cohort Groups5 years post index date during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Here, Overall Number of Participants Analyzed (N) signifies participants who evaluable for this measure with a follow up of 5 years post index date. Reporting groups with N =0 signifies that no participant had a follow up of 5 years post index date.
Percentage of participantsNUMBER
PRIMARYPercentage of Participants Alive After 5 Years From Index Date: Based on Chemotherapy Status5 years post index date during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Here, Overall Number of Participants Analyzed signifies participants who were evaluable for this outcome measure with a follow up of 5 years post index date.
Percentage of participantsNUMBER
PRIMARYPercentage of Participants Alive After 5 Years From Index Date: Based on CNS Metastases Status5 years post index date during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Here, Overall Number of Participants Analyzed signifies participants who were evaluable for this outcome measure with a follow up of 5 years post index date.
Percentage of participantsNUMBER
PRIMARYPercentage of Participants Alive After 5 Years From Index Date: Based on ALK Sequencing, 1 Line of ALK TKI Treatment5 years post index date during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Here, Overall Number of Participants Analyzed signifies participants who were evaluable for this outcome measure with a follow up of 5 years post index date. Reporting arm with Overall Number of Participants Analyzed = 0, signifies that no participant had a follow up of 5 years post index date.
Percentage of participantsNUMBER
PRIMARYPercentage of Participants Alive After 5 Years From Index Date: Based on ALK Sequencing, 2 Lines of ALK TKI Treatment5 years post index date during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Here, Overall Number of Participants Analyzed (N) signifies participants who evaluable for this measure with a follow up of 5 years post index date. Reporting groups with N =0 signifies that no participant had a follow up of 5 years post index date.
Percentage of participantsNUMBER
PRIMARYPercentage of Participants Alive After 5 Years From Index Date: Based on ALK Sequencing, 3 Lines of ALK TKI Treatment5 years post index date during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Here, Overall Number of Participants Analyzed (N) signifies participants who evaluable for this measure with a follow up of 5 years post index date. Reporting groups with N =0 signifies that no participant had a follow up of 5 years post index date.
Percentage of participantsNUMBER
PRIMARYPercentage of Participants Alive After 5 Years From Index Date: Based on ALK Sequencing, More Than or Equal to (>=) 4 Lines of ALK TKI Treatment5 years post index date during data identification period of 9 years (retrieved data assessed in this observational study for approximately 3 months)
Analysis population included all eligible participants whose data were retrieved from Swedish administrative registers and assessed. Here, Overall Number of Participants Analyzed signifies participants who were evaluable for this outcome measure with a follow up of 5 years post index date.
Percentage of participantsNUMBER

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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