Aspects of Quality of Life During Adjuvant Oncological Treatment for Locally Advanced Lung Cancer Which Include Immune Checkpoint Inhibitor.

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorGöteborg University

About this trial

Current oncological treatment for patients with locally advanced lung cancer comprise adjuvant immunotherapy (immune checkpoint inhibitors-ICI) as an additional one-year treatment after chemoradiotherapy which increases overall survival and progression-free survival. Patients with lung cancer have a high burden of distressful symptoms at diagnosis and during chemoradiotherapy. Side-effects from immunotherapy differs, they are unspecific and may develop at any point during treatment. However, it is not investigated thoroughly during adjuvant treatment in locally advanced lung cancer. As new oncological treatments are being introduced, focus must be placed on patients quality of life and how patients endure treatment to be able to know how to best support patients during this treatment. The knowledge gained from this project include how adjuvant immunotherapy treatment impacts health. This knowledge is sparse due to the novelty of the treatment.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with locally advanced non-small lung cancer

cared for at either one of two specialized oncology centres

≥ 18 years of age

planned for concurrent chemoradiotherapy including ICI for 12 months

Disqualifiers

diseases or comorbidities that may have significant impact on the outcome variables

limited understanding of the Swedish language preventing the possibility to give oral and written informed consent.

Trial population

Patients cared for at a specialized oncology centre in Västra Götaland, Sweden and at a regional hospital in Jönköping region in Sweden.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

75 Participants
are grouped into 1 trial group
Group A: Patients with locally advanced lung cancer cared for at two specialized oncology centres.

Trial outcomes

Primary outcomes

1

Changes in aspects of Quality of life (totalscore and subscale scores) during oncological treatment measured with the questionnaire EORTC QLQ C30.

Changes between baseline and 12 months after start of immunotherapy will be assessed with the European Organisation for Research and Treatment of Cancer Quality of life scale (EORTC QLQ-C30). The 30 item instrument measure quality of life in patients with cancer. Scores range from 0-100 where a higher score represents higher quality of life.

Time frame
From enrollment before oncological treatment up til 18 months after start of treatment

Secondary outcomes

1

Changes in self-reported health during oncological treatment measured with EQ-VAS.

Changes in general health will be assessed with EQ-VAS which is a visual analogue scale, measuring a persons overall health-related quality of life. The scale ranges from 100 (the best health you can imagine) to 0 (the worst health you can imagine').

Time frame
From enrollment before oncological treatment up til 18 months after start of treatment
2

Changes in Quality of life specifically in patients with lung cancer during oncological treatment measured with the questionnaire EORTC QLQ - LC13.

A lung cancer module to assess quality of life when having a lung cancer. The European Organisation for Research and Treatment of Cancer Quality of life in lung cancer scale EORTC QLQ - LC13 comprise 13 items, scores range from 0-100 where a higher score represents better quality of life.

Time frame
From enrollment before oncological treatment up til 18 months after start of treatment
3

Changes in well-being related to immune checkpoint modulators during oncological treatment measured with the questionnaire FACT-ICM.

Functional Assessment of Cancer Therapy - Immune Checkpoint Modulator (FACT ICM) comprise 52 items (5 point Likert-type response alternatives between 0 not at all -4 very much). Higher scores indicates better well-being.

Time frame
From enrollment before oncological treatment up til 18 months after start of treatment
4

Changes in existensial health during oncological treatment measured with the questionnaire FACIT-Sp-12.

Functional Assessment of Chronic Illness Therapy -Spiritual Well-Being 12 Item Scale (FACIT-Sp-12) measures perceived existensial health with a 5 point Likert-type scale (0 not at all - 4 very much), higher score indicates better perceived existensial health.

Time frame
From enrollment before oncological treatment up til 18 months after start of treatment

Other outcomes

1

Changes in health promoting factors during oncological treatment assessed with SEMCD-4.

A person's self-efficacy asessed with Self-Efficacy to Manage Chronic Disease (SEMCD) Scale. With the SEMCD the patient rate confidence related to four tasks on a 1 to 10 scale (1 not at all confident" and 10 totally confident). A higher score indicates better self-efficay.

Time frame
From enrollment before oncological treatment up til 18 months after start of treatment
2

Perceived quality of care during onocological treatment measued with GPCCQ 1.0 Scale.

The Generic Person-centred Care Questionnaire (GPCCQ) assess patients experiences of Personcentredness in Care. Totally 18 items assess perceived personcentredness on a likert scale from 1 not at all to 5 completely. A higher score indicates higher personcentredness.

Time frame
From enrollment before oncological treatment up til 18 months after start of treatment

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Göteborg University

Lead sponsor

Västra Götalandsregionen

Collaborator

Region Jönköping County

Collaborator