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Observational Study on Quality of Life of Patients Receiving Nab-paclitaxel/Gemcitabine First Line Therapy, Including a Translational Program

Non-interventional Study on Quality of Life, Efficacy and Tolerability of Nab-paclitaxel/Gemcitabine Firstline Therapy in Patients With Metastatic Pancreatic Cancer

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02691052
Acronym
QoliXane
Enrollment
600
Registered
2016-02-25
Start date
2014-12-31
Completion date
2019-07-31
Last updated
2020-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metastatic Pancreatic Cancer

Keywords

pancreatic cancer, metastatic

Brief summary

Current studies resulted in a superiority of a combination of nab-paclitaxel and gemcitabine vs. gemcitabine mono therapy, but no data are available yet on the quality of life (QoL) under this combination therapy. In the framework of a German multicenter prospective, observational study ('QoliXane'), detailed QoL-data are now collected. QoL development under treatment will be analyzed and data will be compared to existing data of the gemcitabine mono therapy. QoL and course of therapy are collected using the EORTC C30 questionnaires once a month over a 6-month period. Additionally patients are requested to answer a supplementary questionnaire addressing e.g. fears related to QoL deterioration and side effects of chemotherapy. Primary endpoint is the proportion of patients with maintained Global Health Status/QoL at 3 months (10 points threshold). 600 patients shall be enrolled at about 90 study sites in Germany.

Interventions

OTHERQuality of Life questionnaire

EORTC QLQ-C30 questionnaire

Sponsors

Trium Analysis Online GmbH
CollaboratorINDUSTRY
mca Berlin
CollaboratorUNKNOWN
Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* metastatic pancreatic carcinoma * no previous therapy in the metastatic stage * planned firstline therapy with nab-paclitaxel and gemcitabine

Exclusion criteria

* previous therapy in the metastatic stage * patient unable to understand the study and to give informed consent * patient unable to answer quality of life questionnaires

Design outcomes

Primary

MeasureTime frameDescription
Global Health Status/Quality of Life Score at 3 months3 monthsRate of patients without deterioration of their global health status/quality of life score according to EORTC QLQ-C30 after 3 months

Secondary

MeasureTime frameDescription
Limited Baseline Condition3 and 6 monthsRate of patients with a limited baseline general condition (ECOG 2 or 3) and stable or improved Global Health Status/Quality of Life Score after 3 and 6 months
Therapy effects on Global Health Status/Quality of Life Score3 monthsEffect of therapy on Global Health Status/Quality of Life Score and other symptoms and scales assessed by EORTC QLQ-C30: rate of patients with improved, stable or deteriorated score
Prognostic validity of Global Health Status/Quality of Life Score as assessed by tumor response and EORTC QLQ-C306 months
Median time until definitive deterioration of Global Health Status/Quality of Life Score and other functional and symptom scales of EORTC QLQ-C306 months
Influence of Neuropathy on Quality of Life compared to other treatment-related adverse events as assessed by CTCAE v4.06 months
Comparison of Global Health/Quality of Life scores as assessed by EORTC QLQ-C30 to historical Global Health/Quality of Life score data of gemcitabine mono-therapy6 months
Global Health Status/Quality of Life Score at 6 months6 monthsRate of patients with an improvement of their global health status/quality of life score according to EORTC QLQ-C30 after 6 months
Progression free survival as assessed by tumor response6 months
Overall survival as assessed by survival data one year after patient enrollment1 year
Efficacy in high ECOG and high bilirubin patients6 months
Adverse events6 months
Adverse events in special subgroups like high ECOG or high bilirubin patients6 months
Correlations of tumor response and survival with genetic alterations6 months
Tumor response (RECIST)6 months

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026