Background

The burden of mucormycosis has increased with the expansion of risk groups and improved diagnosis. Although diabetes mellitus has been the leading risk factor for mucormycosis globally, the emergence of risk groups such as hemato-oncology patients, allogeneic bone marrow transplantation and solid organ transplantation have shifted the epidemiology of mucormycosis. There is a paucity of literature describing the burden, clinical presentation, treatment and outcomes of mucormycosis in Canada. CANMUS (Canadian Mucormycosis Study)is a national registry with broad geographical representation ,that will assess the epidemiology and clinical outcomes of Canadian patients affected by mucormycosis. Here we assess the outcomes at 6 and 12 weeks of therapy and last clinical assessment.

Methods

This retrospective registry involving 15 centers across Canada, from 1/1/2009 to 1/31/2020 using pathology/microbiology records to identify proven cases of mucormycosis in patients ≥18 years of age. Patient medical record data were collected and reported in a web-based data management program (REDCap). Descriptive statistics analyzed both categorical and continuous data. Cox proportional hazards models were used to explore risk factors for 6 and 12-week survival. Logistical regression was employed to investigate factors associated with positive clinical outcomes (defined as partial or complete response versus stable disease or progression).

Results

Interim data was available on 108 patients. The mean age was 53 (range 20-91) and 55.6% were male patients. The leading diagnostic risk factor for mucormycosis was hematological malignancy (50.9%, of which AML comprised 54.5%) followed by diabetes mellitus (25%). The most common sites of infection were: pulmonary (42.6%) rhino-sinus and/or orbital and/or cerebral (22.2%) and cutaneous (18%). The distribution of pathogens was: Mucor spp. (45.2%), Rhizopus spp. (34.5%) and Lichtheimia spp. (10.7%). Clinical response (composite of complete and partial responses) at 6 and 12 weeks was 31% and 29%, respectively. Survival analyses will be presented using hazard ratios and confidence intervals (CI). Logistic regression of factors associated with a positive clinical response will also be presented.

Conclusions

The epidemiology of mucormycosis in Canada is evolving. Hematological malignancies rather than diabetes are the major predisposing risk factor for mucormycosis with Mucor spp. being the predominant pathogen. Despite modest advances in therapies, outcomes remain poor.

Haider:AVIR Pharma: Consultancy, Honoraria, Research Funding. Mah:AVIR PHARMA: Consultancy. Vinh:Avir Pharma: Consultancy. Bow:Aspergillosis: Other: IDSA/ASCO Clinical Practice Guidelines panel member ; Up-to-date: Other: Section Editor. Faulkner:Avir Pharma: Current Employment. Rotstein:Avir Pharma: Consultancy.

Author notes

*

Asterisk with author names denotes non-ASH members.

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