Daratumumab Provided at Home Experience An Open, Single-center, Mixed-method Project.

This study is a prospective, non-randomized, clinical parallel mixed-methods intervention project using qualitative and quantitative data in the form of semi-structured telephone interviews, focus group interviews, time registration, registration of patients' contact with the healthcare system and PRO data. The project will both include patients already being treated with SC Daratumumab and new patients planned to start Daratumumab treatment = 40 patients in all. The patients will be included in the department of hematology Odense University Hospital as they are found eligible.

The intervention of the study is home administration of Daratumumab SC by a home nurse, thereby, changing the administration setting from a hospital setting to at home setting. The intervention with home administration will be compared to the hospital setting. The patients will function as their own controls, as treatment will be given alternately at the hospital.

Patients scheduled for Daratumumab SC at home will be phoned by a nurse from the Hematology Outpatient Clinic the day before planned administration. This procedure is chosen as that it allows the nurse to determine whether it is justifiable, for the patient to receive treatment at home. If the nurse and doctor assess that the patient is fit for home administration of Daratumumab SC, the drug will be ordered at the pharmacy to be delivered to the patient the following day. Also an electronic message will also be sent to the home nurses with an instruction to administer Daratumumab SC between 12-02 PM.

Data collection will consist of:

• Semi-structured virtual (or alternative telephone) interviews with participating patients focusing on benefits / gains versus challenges / disadvantages in regard to the actual injection, collaboration with the home nurse, delivery of medication, empowerment, and suggestions for further improvements n = 2 x 10
• Semi-structured interviews with involved home nurses n = 1 x 5.
• Focus group interview with health professionals involved at OUH at the end of the project n = 1.
• Registration of unplanned contact to the health service during the study period to account for any extra health care usage during home treatment via the app "My hospital" x 1 weekly n = 40
• Data on quality of life; EORTC custom built satisfaction questionnaire via the app "My hospital" = 5 times per patient.
• Registration of the patients evaluation of whether the use of the app "My hospital" can be useful in the future.
• Registration of patients' time used on treatment when at home or when at hospital including transport via the app "My hospital".
• Registration of the outpatient nurses' and home nurses time using the registration form via paper.
• Registration of patients general condition and possible side effects in order to clarify whether they are "fit" for treatment via the app "My hospital". This ensures that a cure that is not used is not prepared.

All Suspected Unexpected Serious Adverse Reactions (SUSARs) will be reported to the Danish National Health Authorities according national law within 7 days after awareness. Since this is not at clinical trial, but merely a collection of data during a different logistics setup, the study will be submitted to the Danish Data Protection Agency, however not to the Danish National Ethical Committee nor the Danish National Health Authorities. Due to this Adverse Reactions (AEs) will not be systematically registered or reported to the Danish national health authorities. To make sure the logistics setup is safe for all patients we will register all unplanned hospitalizations as well as all other related Serious Adverse Reactions (SAR).

Processing of personal data in the project The project is notified to the Region's Register so that it complies with the Data Protection Regulation (GDPR). All electronic data will be stored on a secure SharePoint site that can only be accessed via the project group's work computer. All physical material is stored behind double-locked doors at the project group's workplace.

Inclusion criteria

• have relapse of MM.
• be in or have planned to start treatment with Daratumumab SC.
• be cognitively capable to assess any side effects of Daratumumab SC based on the instructions provided.
• be able and willing to register in a timetable and to participate in two semi-structured telephone interviews.
• be able to understand and speak Danish.
• be in possession of a mobile phone (for SMS tracking).

Exclusion criteria

• receive other anti-myeloma treatment that require hospitalization with the exception of visit 1 in all cycles with Daratumumab SC administration.