scholarly journals Mycosis fungoides and Sézary syndrome: a population-wide study on prevalence and health care use in Finland in 1998–2016

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Jaana Keto ◽  
Sonja Hahtola ◽  
Miika Linna ◽  
Liisa Väkevä

Abstract Background Information about health care use and costs of cutaneous T-cell lymphoma (CTCL) patients is limited, particularly in a European setting. Methods In this population-wide study we set out to investigate prevalence, and trends in health care use in two CTCL subtypes, mycosis fungoides (MF) and Sézary syndrome (SS) over a time period of 19 years in 1998–2016 by using a nation-wide patient register containing data on all diagnosed MF and SS cases in Finland. Results The prevalence of diagnosed MF and SS rose from 2.04 to 5.38/100000, and from 0.16 to 0.36/100000 for MF and SS respectively during 1998–2016. We found a substantial decrease in inpatient treatment of MF/SS in the past two decades with a mean of 2 inpatient days/patient/year due to MF/SS in 2016, while the mean numbers of MF/SS related outpatient visits remained stable at 8 visits/year/patient. Most MF/SS-related outpatient visits occurred in the medical specialty of dermatology. In a ten-year follow-up after MF/SS diagnosis, the main causes for outpatient visits and inpatient stays were MF/SS itself, other cancers, and other skin conditions. Also cardiovascular disease and infections contributed to the number of inpatient days. Mean total hospital costs decreased from 11,600 eur/patient/year to 3600 eur/patient/year by year 4 of the follow-up, and remained at that level for the remainder of the 10-year follow-up. MF/SS accounted for approximately half of the hospital costs of these patients throughout the follow-up. Conclusions The nearly 3-fold increase in prevalence of diagnosed MF/SS during 1998–2016 puts pressure on the health care system, as this is a high-cost patient group with a heavy burden of comorbidities. The challenge can be in part answered by shifting the treatment of MF/SS to a more outpatient-based practice, and by adapting new pharmacotherapy, as has been done in Finland.

1995 ◽  
Vol 13 (1) ◽  
pp. 257-263 ◽  
Author(s):  
T M Kuzel ◽  
H H Roenigk ◽  
E Samuelson ◽  
J J Herrmann ◽  
A Hurria ◽  
...  

PURPOSE To investigate the efficacy of combined topical therapy and systemic interferon alfa-2a in patients with mycosis fungoides (MF) and the Sézary syndrome (SS). PATIENTS AND METHODS Between December 1987 and April 1993, 39 patients with all stages of MF and SS were treated with combined phototherapy and systemic interferon alfa-2a as part of two institutional studies. The initial phase I study of 15 patients established the maximum-tolerated dose of interferon and has been previously reported. Subsequently, 24 patients have been entered onto a phase II trial. Long-term follow-up data are provided for both studies. RESULTS The median follow-up duration for the entire cohort is 28 months. Patients with all stages of disease were enrolled (stage IB, n = 14; IIA, n = 5; IIB, n = 6; III, n = 8; IVA, n = 5; IVB, n = 1). Thirty-four patients had received previous therapy. Overall, 36 of 39 patients achieved a complete response (CR; 62%) or partial response (28%) to therapy. The median response duration is 28 months (range, 1 to 64). Twenty-nine of 39 patients are alive, with a median survival duration of 62 months (range, 1 to 66). CONCLUSION Interferon alfa-2a combined with phototherapy is an effective, safe, durable therapy for MF and SS.


Blood ◽  
2007 ◽  
Vol 110 (11) ◽  
pp. 3425-3425
Author(s):  
Brady Beltran-Garate ◽  
Henry Gomez ◽  
Jose L. Lopez ◽  
Mildred Borrego ◽  
Mercedes Prieto ◽  
...  

Abstract Background: Alemtuzumab (Campath®/Mabcampath®, anti-CD52 humanized monoclonal antibody) has recently been shown to be effective in the treatment of diverse hematological malignancies. Mycosis fungoides (MF) and Sezary Syndrome (SS) are low grade cutaneous T-cell lymphoma with indolent course and multiple relapsed. Aim: We describe our experience from three centers in South America with refractory/relapsed MF/SS patients treated with Alemtuzumab as monotherapy. Methods: From July 2005 to April 2006 a total of 13 patients were recruited from 2 centers in Lima-Perú and one center in Caracas-Venezuela with histopathology diagnosed of advanced refractory/relapsed MF (10pts) or SS (3pts); median age 60 years old (range: 36–72); 9 pts. were male. Median number of previous therapies 2.5 (range: 2–7). Treatment scheduled was planned as follow: Alemtuzumab 30 mg i.v. tiw per 8 weeks with a gradually escalated doses during the first week (3,10, 30 mg). Trimethoprim/sulphamethoxazole and acyclovir as prophylaxis were given. Median Alemtuzumab total dose was 429 mg (range: 123–706) over a median time of treatment of 6.2 weeks (range:3–15). The first nine pts. received the planned schedule dose; 2 pts. received Alemtuzumab 30 mg i.v. tiw for 4 weeks and then 30 mg i.v. weekly and the last 2 recruited pts. received Alemtuzumab 10 mg iv. tiw for 4 weeks them after 10 mg i.v. biw and finally 10 mg i.v. weekly. CMV monitoring with pp65 was performed in the first five pts. and qualitative PCR in 3 pts. Results: Twelve patients were evaluable for response. Overall response rate (ORR) was 75% (9/12), with three patients achieving complete remission (CR) and six patients with partial response (PR); three patients with progressive disease (PD) during treatment. Responses were seen in 6/9 (75%) MF pts. and 3/3(100%) SS pts. Regarding clinical presentation: 4 over 4 (100%) eritrodermic forms responded and 5 over 8 (62%) tumoral forms responded. Response duration and CMV reactivation were described in table 1. Hematological toxicity was grade 1–2 neutropenia in three pts. and grade 1–2 thrombocytopenia in three pts. One pt. developed urosepsis caused by E. Coli. and 1 pt. had genital herpes. No cardiac toxicity was reported. Kaposi sarcoma progression was discovered in one pt. One pt. died with CMV pneumonitis, three months after treatment, 1 pt. died at two months during treatment for a neurology event Conclusion: Alemtuzumab as monotherapy shows promising clinical activity with sustained response in patients with advanced MF and SS. New studies should be address the Alemtuzumab impact in these malignancies with reduced doses or even combined therapies. Table 1. Outcomes, follow-up and CMV status Alemtuzumab (TD, mg) Response Follow-up (m) CMV Status TD=total dose, NE=no evaluable, AD=active disease, m=months, R=reactivation, F=fever, P=Pneumonitis 123 NE AD, 14 m R with F 313 PD Died, 8 m 706 PD AD, 8 m 403 CR Relapse at 6 m R with F 253 CR Relapse at 3 m. R with F 493 PR PR at 8 m, and death 123 PR Relapse at 3 m R no F 163 PD AD, 3 m R no F 673 CR Relapse at 30 m 673 PR Relapse at 14 m 673 PR Death at 2 m 673 PR PR, 30 m 673 PR PR, 3 m and death R with P


1970 ◽  
Vol 101 (2) ◽  
pp. 244-246 ◽  
Author(s):  
H. H. Roenigk

Sign in / Sign up

Export Citation Format

Share Document