Kyowa Kirin: New Data Analysis Shows Link between Blood Involvement and Response to Treatment in Cutaneous T-cell Lymphoma (CTCL) Patients
Kyowa Kirin International PLC (Kyowa Kirin), a wholly owned subsidiary of Kyowa Kirin Co., Ltd., today announced a new analysis of data showing statistically significant improvements in quality of life in cutaneous T-cell lymphoma (CTCL) patients treated with mogamulizumab with blood involvement, compared to vorinostat.1 The new findings from the MAVORIC trial compared the impact of treatment with POTELIGEO® (mogamulizumab) and vorinostat by patient blood tumour burden in adult patients with mycosis fungoides (MF) and Sézary syndrome (SS), two types of CTCL.
Professor Doctor Pier Luigi Zinzani of the Institute of Hematology "L. e A. Seràgnoli" at the University of Bologna said: “This new analysis helps us to understand more about the importance of blood involvement in CTCL, which is relatively common in the more advanced stages of the disease and may be present in some less advanced cases. We know that increasing levels of malignant T-cells in the blood correlate with increased risk of CTCL disease progression and an overall reduction in patient survival. Treatment with mogamulizumab has also been shown to be more effective in CTCL patients who have blood involvement as part of their disease and treatment with mogamulizumab also generates quality of life benefits for CTCL patients with blood involvement. This new information underlines the importance of blood monitoring in the clinical management of CTCL patients.”
In the study, patients classified as B0 were considered to have no blood involvement and patients classified as B1 and B2 were considered to have blood involvement.1 B1 is a measurable low level of blood involvement of between 250 to 1000 abnormal T-cells per µL. B2 is higher level of blood involvement, greater than 1000 abnormal T-cells per µL, detected using flow cytometry.
Statistically significant differences in quality of life were seen for patients with blood involvement, with patients treated with mogamulizumab seeing improvements in the Skindex-29 and ItchyQoL questionnaires, compared to vorinostat. Quality of life improvements were also seen in patients treated with mogamulizumab with blood involvement assessed by the Pruritus Likert Scale and the FACT-G Total Score questionnaires, compared to vorinostat. For patients with no blood involvement there was no statistically significant differences in quality of life between mogamulizumab and vorinostat.1
MF and SS are subtypes of CTCL, a rare type of non-Hodgkin's lymphoma that can affect the skin, blood, lymph nodes and internal organs.2 As a chronic and generally incurable disease associated with disfiguring skin lesions, intractable itching, sleep disturbance, and psychosocial problems, CTCL has a serious negative effect on quality of life.1 MAVORIC is the largest multinational, randomised, Phase 3 trial of systemic CTCL therapy. MAVORIC evaluated the safety and efficacy of mogamulizumab versus vorinostat in patients who had received at least one previous systemic therapy.3 This new post hoc analysis of the MAVORIC trial looked at data from patients’ quality of life using a range of recognised and validated assessment tools.1
The MAVORIC trial met its primary endpoint of overall investigator-assessed progression-free survival (PFS), which was shown to be significantly greater for patients treated with mogamulizumab compared to vorinostat, at 7.7 months and 3.1 months, respectively (P<0.0001).3
About Mycosis Fungoides (MF) and Sézary syndrome (SS)
Cutaneous T-cell lymphomas (CTCL) are rare, serious and potentially life-threatening, forms of non-Hodgkin’s lymphoma,2 affecting around 240 persons per 1,000,000 population across Europe.4 Mycosis fungoides (MF) and Sézary syndrome (SS) are the two best studied types of CTCL,5 together accounting for around two thirds of all CTCLs.6,7
MF and SS can affect the skin, blood, lymph nodes (part of the body’s immune system which is spread throughout the body) and internal organs.2 MF and SS can be very distressing for patients and have a significant negative impact upon many aspects of patients’ lives.3,8 Disease stage in MF and SS is the most important prognostic factor,9 and draws upon the type and extent of skin involvement, as well as the presence or absence of extracutaneous disease in lymph nodes, viscera, and blood.10 Hence, assessment of all four anatomical ‘compartments’ is recommended, first at diagnosis and then to assess patient response to treatment.10,11
Neoplastic T lymphocytes in MF and SS, consistently express CC chemokine receptor 4 (CCR4),3 making this a relevant target for treatment at all stages of disease. All disease stages can include blood involvement10,12 and blood tumour burden may be relevant for prognosis13 and treatment6,10,14,15 in MF and SS.
Due to its likeness to more common skin conditions such as eczema and psoriasis,16 CTCL can take, on average, between 2 and 7 years for individuals to receive a confirmed diagnosis.17 It is critical for doctors to accurately diagnose CTCL as early as possible as the patient’s prognosis can be affected if the disease progresses to later stages.13 Whilst most individuals that present with early stage do not progress to a more advanced stage,18 patients with advanced disease have significantly poorer outcomes with only around half of patients (52%) surviving for just 5 years.19
About POTELIGEO (mogamulizumab) and the MAVORIC Trial
POTELIGEO (mogamulizumab), a humanised monoclonal antibody that selectively binds to CCR4,20 elicits anti-tumour activity by antibody-dependent cellular cytotoxicity (ADCC).3
Following a positive opinion from Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA), the European Commission (EC) granted marketing authorisation for mogamulizumab in November 2018 for the treatment of adult patients with MF or SS who have received at least one prior systemic therapy.20 The CHMP’s opinion was based on results of the MAVORIC trial, the largest randomised study of systemic therapy in MF and SS,3 and the first trial to compare systemic therapies using progression-free survival as a primary endpoint.3
MAVORIC evaluated the safety and efficacy of mogamulizumab versus vorinostat in patients who had received at least one previous systemic therapy:3
- Mogamulizumabmore than doubled median progression-free survival (PFS) in patients with relapsed or refractory MF/SS, compared with vorinostat (7.7 months vs 3.1 months), which is a relative reduction in the risk of disease progression of 47% (HR=0.53, 95% CI: 0.41–0.69; P<0.0001). 3
- Overall, significantly more patients responded to mogamulizumab than vorinostat (overall response rate [ORR] 28.0% versus 4.8% (P<0.0001). 3
- Median time-to-next-treatment (TTNT), an additional measure of clinical benefit and disease control, was significantly superior in patients treated with mogamulizumab compared to those that received vorinostat (11.0 months vs 3.5 months; P<0.0001). 3
- In post hoc analyses, patients with B1 and B2 levels of blood tumour burden that received mogamulizumab have been shown to draw significantly more benefit in terms of PFS,21 TTNT, 21 and improvement in mSWAT22 compared to patients that received vorinostat.
- Mogamulizumab shows good tolerability with a manageable safety profile. 3,23,24,25
Important Prescribing information and Safety Information
Refer to the full Summary of Product Characteristics (SmPC) for prescribing information and the full safety information: https://www.ema.europa.eu/en/medicines/human/EPAR/poteligeo#product-information-section
About Kyowa Kirin
Kyowa Kirin strives to create and deliver novel medicines with life-changing value. As a Japan-based Global Specialty Pharmaceutical Company with a heritage of 70+ -years, we apply cutting-edge science including an expertise in antibody research and engineering, to address the needs of patients and society across multiple therapeutic areas including Nephrology, Oncology, Immunology/Allergy and Neurology. Across our four regions – Japan, Asia Pacific, North America and EMEA/International – we focus on our purpose, to make people smile, and are united by our shared values of commitment to life, teamwork/Wa, innovation, and integrity. You can learn more about the business of Kyowa Kirin at: https://www.kyowakirin.com/
Kyowa Kirin International
http://www.international.kyowa-kirin.com / www.kyowakirin.com
Galabank Business Park
Galashiels, TD1 1QH
United Kingdom
References
1 EHA 2021 abstract. Available at: HEALTH-RELATED QUALITY OF LIFE EFFECT OF MOGAMULIZUMAB BY PATIENT.... EHA Library. Bishton M. Jun 9 2021; 324119 (ehaweb.org). Accessed June 2021
2 Olsen E, Vonderheid E, Pimpinelli N, et al. Revisions to the staging and classification of mycosis fungoides and Sezary syndrome: a proposal of the International Society for Cutaneous Lymphomas (ISCL) and the cutaneous lymphoma task force of the European Organization of Research and Treatment of Cancer (EORTC). Blood. 2007;110(6):1713-22.
3 Kim YH, et al. Lancet Oncol. 2018;19(9):1192–1204.
4 Orphanet. Prevalence and incidence of rare diseases: Bibliographic data. January 2020. Accessed December 2020.
5 Krejsgaard T, et al. Semin Immunopathol. 2017;39:269–282.
6 Trautinger F, et al. Eur J Cancer. 2017;77:57–74.
7 Willemze R, et al. Blood. 2019;133(16):1703–1714.
8 Demierre M, et al. Cancer. 2006;107(10):2504–2511.
9 Hughes CF, et al. Australas J Dermatol. 2016;57(3):182–191.
10 Olsen EA, et al. J Clin Oncol. 2011;29(18):2598–2607.
11 Scarisbrick, J. EMJ Hematology. 2018;6(1):92–100.
12 Scarisbrick J, et al. Eur J Cancer. 2018;93:47–56.
13 Agar N, et al. J Clin Oncol. 2010;28(31):4730–4739
14 Willemze R, et al. Ann Oncol. 2018;29(4):iv30-iv40.
15 National Comprehensive Cancer Network (NCCN). Clinical Practice Guidelines in Oncology (NCCN Guidelines®): Primary Cutaneous Lymphomas (Version 1.2021 – October 12, 2020)
16 Scarisbrick J, at al, J Clin Oncol 2015;33(32):3766-3773
17 CL Foundation: A Patient’s Guide. Available from: https://www.clfoundation.org/sites/default/files/2018-04/a_patients_guide.pdf. Last Accessed: September 2020
18 Krejsgaard T, Lindahl LM, Mongan NP, et al. Malignant inflammation in cutaneous T-cell lymphoma—a hostile takeover. Semin Immunopathol. 2017;39(3):269–282.
19 KIM YH, et al. Blood 2019; 134(1):269-282
20 POTELIGEO® (mogamulizumab) Summary of Product Characteristics.
21 Scarisbrick J, et al. Efficacy and Safety of Mogamulizumab by Patient Blood Classification. Poster presented at: European Association of Dermato Oncology (EADO); 12–14 October, 2020. Vilnius, Lithuania.
22 Quaglino P, et al. he Correlation Between Skin Response and Blood Involvement with Mogamulizumab. Poster presented at: European Association of Dermato Oncology (EADO); 12–14 October, 2020. Vilnius, Lithuania.
23 Duvic M, et al. Blood. 2015;125(12):1883–1889
24 Ogura M, et al. J Clin Oncol. 2014;32(11):1157–1163
25 Yamamoto K, et al. J Clin Oncol. 2010;28(9):1591–1598
To view this piece of content from cts.businesswire.com, please give your consent at the top of this page.
View source version on businesswire.com: https://www.businesswire.com/news/home/20210610005352/en/
Contact information
Contacts for Kyowa Kirin International:
Media
Stacey Minton
+44 (0) 7769 656073
Email: Stacey.Minton@kyowakirin.com
About Business Wire
For more than 50 years, Business Wire has been the global leader in press release distribution and regulatory disclosure.
Subscribe to releases from Business Wire
Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.
Latest releases from Business Wire
Helical Fusion Signs Japan’s First Power Purchase Agreement for Fusion Energy with Aoki Super8.12.2025 11:00:00 EET | Press release
Helical Fusion Co., Ltd. (Headquarters: Tokyo, Japan; “Helical Fusion”), a company developing a commercially viable Helical Stellarator power plant under its “Helix Program”, has signed a Power Purchase Agreement (PPA) with Aoki Super Co., Ltd. (Headquarters: Aichi, Japan; “Aoki Super”), a major regional supermarket chain in central Japan. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20251207372064/en/ Takaya Taguchi (left), CEO of Helical Fusion Co., Ltd. , and Masayuki Kono (right) Managing Director and Head of Administration Division of Aoki Super Co., Ltd. at the press conference held on December 8, 2025 This marks the first fusion-energy PPA ever signed in Japan, representing a concrete step forward in the real-world adoption of fusion energy and signaling growing demand-side engagement in the emerging fusion energy value chain. Significance of This Agreement Fusion energy—generated by reproducing on Earth the same nucl
Tecnotree Mentioned in Various 2025 Gartner® Research8.12.2025 10:41:00 EET | Press release
Tecnotree is a 5G-ready digital Business Support System (BSS) provider with advanced AI/ML capabilities and multi-cloud extensibility. The company has been listed across thirteen 2025 Gartner research spanning Digital BSS, AI-driven monetization, digital marketplace enablement, and customer experience transformation. We believe these mentions reflects the continued relevance and strong applicability of Tecnotree’s solutions within the technology domains evaluated by Gartner. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20251208688494/en/ Tecnotree Mentioned in Various 2025 Gartner® Research The research span Market Guides, Hype Cycles, Magic Quadrants, Critical Capabilities, and Competitive Landscape reports, which we think collectively provides an overview of how various technologies are evolving across the communications ecosystem. We believe that Tecnotree’s appearance across these research categories underscores what we
ATEC2025·Real-World Extreme Challenge Concludes with Zhejiang University Team Claiming $150,000 Prize for Breakthrough in Fully Autonomous Robotics8.12.2025 10:25:00 EET | Press release
The ATEC2025·Real-World Extreme Challenge successfully concluded on December 7 on the campus of The Chinese University of Hong Kong. A team from Zhejiang University emerged victorious from a field of 13 talented international squads by demonstrating exceptional fully autonomous embodied intelligence, securing the top prize of $150,000 USD. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20251207877880/en/ A Zhejiang University team wins ATEC2025·Real-World Extreme Challenge Organized by the Chinese University of Hong Kong and co-hosted by Advanced Technology Exploration Community (ATEC), Peking University, Beijing Normal University, and Ant Group, ATEC2025·Real-World Extreme Challenge was the world’s first intelligent robotics challenge held entirely outdoors on natural terrain—featuring rugged hills, stone steps, swaying bridges, and uneven slopes—to rigorously test robots’ ability to operate without human intervention. Under
AI Won't Transform Mobility Without Unprecedented Collaboration, Study Reveals8.12.2025 10:25:00 EET | Press release
Artificial intelligence is quietly reshaping global transportation systems, but most deployments remain isolated pilots that haven't achieved scale – and the gap between AI's promise and its execution is widening, according to a landmark study launched today at CoMotion GLOBAL in Riyadh. The Envisioning the Future of Mobility Powered by AI report, developed by the MIT Mobility Initiative and Kearney Advanced Mobility Institute, analyzed input from 55 leading global organizations, including Google, Lyft, Uber Freight, Deutsche Bahn, and NEOM. The study mapped real-world AI applications across mobility systems in Europe, the Americas, APAC, and the Middle East – revealing both breakthrough potential and fundamental challenges in bringing AI-powered mobility to scale. The report identifies a critical dynamic reshaping the industry: AI doesn't simply replicate human intelligence – it excels dramatically in some functions while failing unpredictably in others. This "jagged frontier" creates
SIAL Paris 2026 : The Entire Food Industry in One Place – An Unmissable Event for Professionals8.12.2025 10:00:00 EET | Press release
With less than a year to go, SIAL Parisonce again stands as a key international gathering for food industry professionals. With 85% of exhibition space already booked, the show demonstrates very strong momentum and appeal. SIAL Paris will welcome 295,000 professionals from 200 countries across a stunning 280,000 m² of exhibition space, covering all sectors of the food industry. Innovation at the core of global food transformation In a context marked by major demographic, environmental and geopolitical challenges, SIAL Paris stands as THE hub where innovation drives action, business, and transformation. It brings across all sectors’ ideas, projects, and solutions that address today’s challenges, all while inspiring food business around the world. As in every edition, the show will offer a unique immersive experience, facilitating meaningful meetings and business opportunities. SIAL Paris serves as the global international showcase for food innovation, allowing brands and companies to ex
In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.
Visit our pressroom
