International study of treatment efficacy in SS shows superiority of combination therapy and heterogeneity of treatment strategies

Author:

Campbell Belinda A.123ORCID,Dobos Gabor45ORCID,Haider Zahra6,Prince H. Miles27ORCID,Bagot Martine4ORCID,Evison Felicity8,van der Weyden Carrie27ORCID,McCormack Chris910,Ram-Wolff Caroline4,Miladi Maryam4,Scarisbrick Julia J11ORCID

Affiliation:

1. 1Department of Radiation Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia

2. 2Sir Peter MacCallum Department of Oncology, The University of Melbourne, Parkville, Australia

3. 3Department of Clinical Pathology, The University of Melbourne, Parkville, Australia

4. 4Department of Dermatology, Hôpital Saint Louis, Université Paris Cité, Paris, France

5. 5Department of Dermatology and Allergy, Charité – Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany

6. 6Department of Dermatology, Queen Elizabeth Hospital, Birmingham, United Kingdom

7. 8Department of Haematology, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne Australia

8. 7Health Data Science Team, Research Development and Innovation, University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom

9. 9Department of Surgical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia

10. 11Department of Surgery, The University of Melbourne, Parkville, Australia

11. 10Department of Dermatology, University Hospital Birmingham, Birmingham, United Kingdom

Abstract

Abstract Despite increasing availability of therapies, patients with Sezary syndrome (SS) commonly endure multi-line treatment journeys, mostly with partial responses of short duration. Measuring clinical benefit is challenging; time-to-next-treatment (TTNT) provides a robust, objective measurement of efficacy. This international observational study examines patterns of clinical care and therapeutic benefit as measured by TTNT. TTNT was calculated for monotherapies and combination therapies, with consideration to treatment line. 178 patients with SS (73% de novo, 27% secondary) were included, receiving 721 lines of systemic therapy, with median follow-up of 56.9 months. Across all lines, 58 different therapeutic regimens were prescribed (54 were systemic therapies) and classified into 17 treatment groups. The most common first-line treatments were extracorporeal photopheresis (ECP)–containing combination therapy (20%) and retinoid monotherapy (19%). Median TTNT for all first-line therapies was short (5.4 months). First-line, combination therapies had longer median TTNT than monotherapies, 10.0 vs 5.0 months (P = .004), respectively. Later delivery of combination therapies was associated with shorter clinical benefit, with median TTNT reduced to 6.2 and 2.2 months for mid-line (2nd-4th line) and late-line (≥5th line), respectively (P < .001). First-line ECP-containing treatments were associated with longer median TTNT than non-ECP–containing treatments, 9.0 vs 4.9 months (P = .007). For both ECP-monotherapy and ECP–containing combination therapy, significant reductions in TTNT were seen in later lines. These data suggest therapeutic benefit from first-line delivery of combination therapy for SS and favor early inclusion of ECP in the treatment algorithm for those who can access it.

Publisher

American Society of Hematology

Subject

Hematology

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