The overall survival for patients with lymphoma has increased in recent decades due to advances in treatment. An increasing number of patients with lymphoma thus are becoming long-term survivors, which entails a risk of late toxicities associated with the chemotherapy regimens used to treat their lymphoma. The aim of this PhD research was to investigate these late toxicities in a real-world setting by establishing associations, risks, and risk factors. This PhD thesis includes four population-based epidemiological cohort studies: Study I showed an increased risk of congestive heart failure and cardiovascular diseases in general, respectively, for patients with follicular lymphoma or diffuse large B-cell lymphoma treated with anthracycline-containing immunochemotherapy compared to patients treated without. Furthermore, a dose-response relationship was established.Study II was focused on the risk of new-onset steroid-induced diabetes mellitus for patients with non-Hodgkin lymphoma treated with steroid-containing immunochemotherapy compared to a matched background population and identified no significantly increased risk. However, patients with pre-existing diabetes mellitus treated with steroid-containing immunochemotherapy had an increased risk of first insulin prescriptions compared to matched comparators with pre-existing diabetes mellitus.Study III showed an increased risk of second primary malignancies for patients with aggressive lymphoma treated with high-dose therapy with autologous stem cell transplant (HDT-ASCT) compared to a matched background population and patients treated without HDT-ASCT, respectively. The increased risk was driven by an increased risk of non-melanoma skin cancer and myelodysplastic syndrome/acute myeloid leukemia, but not solid tumors.
ABBREVIATIONSABVD Adriamycin, bleomycin, vinblastine, dacarbazine AML Acute myeloid leukemia ASCT Autologous stem cell transplantation ATC Anatomical Therapeutic Chemical Classification System Axi-cel Axicabtagene ciloleucel (E)-BEACOPP (Escalated) Bleomycin, etoposide, adriamycin, cyclophosphamide, vincristine, procarbazine, prednisone BEAM Carmustine, etoposide, cytarabine, melphalan BV Brentuximab vedotin CAR-T Chimeric antigen receptor T cell CD Cluster of differentiation CHF Congestive heart failure CHOEP Cyclophosphamide, doxorubicin, vincristine, etoposide, prednisone CHOP Cyclophosphamide, doxorubicin, vincristine, prednisone CI Confidence interval CNS Central nervous system CoxPH Cox proportional hazards CPR Civil personal register CVD Cardiovascular disease CVP Cyclophosphamide, vincristine, prednisone