Effects of chemotherapy dose reductions in overweight patients with acute myeloid leukaemia: A Danish nationwide cohort study

Daniel Tuyet Kristensen*, Lars Børty Nielsen, Lasse Hjort Kyneb Jakobsen, Tove Christina Choe Kristensen, Lene Østergaard Jepsen, Claudia Schöllkopf, Kim Theilgaard-Mönch, Tarec Christoffer El-Galaly, Anne Stidsholt Roug, Marianne Tang Severinsen


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Overweight patients with cancer are frequently reduced in chemotherapy dose due to toxicity concerns, although previous studies have indicated that dose reduction (DR) of overweight patients results in comparable toxicity but may compromise overall survival (OS). Current evidence regarding DR in patients with acute myeloid leukaemia (AML) is limited. To investigate the association between DR and outcome among overweight patients with AML we analysed a Danish nationwide cohort of overweight adult AML patients treated with remission induction chemotherapy. Among 536 patients identified, 10.1% were categorized as DR defined as 95% or less of full body surface area (BSA)-based dose. Risk factors for DR were high body mass index (BMI) and BSA, therapy-related AML and favourable cytogenetics. No significant differences were observed for rates of complete remission (CR), 30- and 90-day mortality between DR and non-DR patients. Furthermore, DR did not affect median relapse-free survival (RFS) [DR, 14.5 (95% confidence interval, 9.0–41.7) months; non-DR, 15.0 (12.3–19.3)] with an adjusted difference in five-year restricted mean survival time (Δ5y-RMST) of 0.2 (−8.4 to 8.8) months nor median OS (DR, 17.0 [11.9 to 45.5] months; non-DR, 17.5 [14.8 to 20.5]) with an adjusted Δ5y-RMST of 0.8 (−5.7 to 7.3) months. In conclusion, we found no statistically significant association between DR and outcomes among overweight patients with AML. However, we acknowledge the limited sample size and encourage further studies in this important subject.

TidsskriftBritish Journal of Haematology
Udgave nummer4
Sider (fra-til)539-548
StatusUdgivet - nov. 2022

Bibliografisk note

Funding Information:
Our profound gratitude to everyone who has participated in forming and collecting data for The Danish Acute Leukaemia Registry (DNLR) and The Danish Clinical Quality Program—National Clinical Registries (RKKP) for providing and governing the data. Financial support for this study was provided by the Danish Cancer Society (Grant R94‐A5768‐B2403) (for Marianne T. Severinsen).


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