New systemic treatment options in mycosis fungoides and Sézary syndrome

Cutaneous T cell lymphomas (CTCL) are a heterogeneous group of rare non-Hodgkin lymphomas characterized by infiltration of neoplastic T lymphocytes to the skin. The most common type of CTCL is mycosis fungoides (MF). Much less common but clinically and histopathologically related to MF is Sézary syndrome (SS) [1]. Reported age-adjusted incidence rates per 100,000 person-years in the United States (US) between 2005 and 2008 were 0.55 for MF and 0.01 for SS [2]. The clinical presentation and prognosis of MF vary widely and depend on clinical stage, ranging from limited skin involvement with patches and plaques to severe illness with ulcerated skin tumors, systemic involvement and death [3]. SS, which is more aggressive and clinically staged IVA-IVB [4], is defined by pruritic erythroderma, generalized lymphadenopathy and leukemic involvement [1]. CTCL are incurable and associated with a reduced quality of life [3, 5]. While early stage MF has a good prognosis and is usually treated with skin directed therapies, median survival ranges from 4.7 to 1.4 years in advanced stages of MF and SS (clinical stage IIB–IVB) [6]. Systemic therapies are then required, including retinoids, interferon alpha, cytotoxic chemotherapeutic drugs, low-dose methotrexate, histone deacetylase inhibitors (vorinostat, romidepsin, belinostat) and alemtuzumab [3]. However, relapses are frequent and long-term remissions are achieved only in few cases, e.g. with allogenic stem cell transplantation [7]. In recent years new therapeutic options have evolved. These are discussed in detail in the following article.

CD30, a cell surface receptor, is uniformly expressed in Hodgkin lymphoma (HL) and anaplastic large cell lymphoma (ALCL) [8]. In CTCL CD30 expression is commonly seen in primary cutaneous anaplastic large-cell lymphoma (pc-ALCL) and lymphomatoid papulosis [1] and less frequently in MF and SS at various levels, ranging from 20–40% [9‐11]. Brentuximab vedotin (BV) is an anti-CD30 antibody conjugated to the cytotoxic antitubulin agent monomethyl auristatin E (MMAE). The interaction between this complex and the CD30 ligand on lymphocytes leads to internalization into the cell where MMAE is released and causes an interruption of the microtubule network, inducing cell-cycle arrest and apoptosis. In addition, a small fraction of MMAE is released from CD30+ cells, killing neighboring cells in the tumor microenvironment in a CD30-independent manner [12]. In November 2017 the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA) approved BV for patients with CD30+ CTCL that have received at least one systemic therapy [13, 14], based on the results of the ALCANZA study [15]. In this phase 3 trial, 97 patients with CD30+ MF and 31 patients with pc-ALCL pretreated with at least one systemic therapy or radiotherapy were randomly assigned to BV (intravenously 1.8 mg/kg every 3 weeks for up to 16 cycles) or to physician’s choice (oral methotrexate 5–50 mg qw or oral bexarotene 300 mg/m² qd). CD30 expression of at least 10% of malignant cells or lymphoid infiltrate in skin biopsies was required. The primary endpoint was the percentage of patients achieving an overall response rate (ORR) persistent for at least 4 months (ORR4). This was reached in 50% of the MF patients in the BV group and in 10% in the physician’s choice group. Responses to BV were seen in all clinical stages, albeit patients with SS were excluded from this study and approximately 3/4 of included patients had lower grade disease (stage IA-IIB). The progression free survival (PFS) was 15.9 months in the BV arm versus 3.5 months in the control arm. Side effects were similar to previous reports. The most common adverse event (AE) observed in the BV group was peripheral neuropathy (67%), which usually resolved after treatment discontinuation. Grade 3–4 AEs were reported in 41% of patients in the BV group and in 47% in the physician’s choice group. One death was considered to be treatment related in the BV group. In sum, this study showed efficacy of BV in the treatment of refractory or relapsed CD30+ MF with CD30 expression levels of at least 10% [15]. Notably, in two smaller phase 2 trials the efficacy of BV was also demonstrated in CD30+ SS as well as in MF/SS with CD30 expression levels below 10% [16, 17], although response in patients with CD30 expression levels below 5% was poor (17%) [16], suggesting that response to BV appears to be independent of CD30 expression only in patients with expression levels over 5–10%. Ongoing studies are examining BV in combination with other substances like nivolumab, romidepsin and lenalidomide in CTCL patients (Tables 1 and 2; [18]).

C‑C chemokine receptor type 4 (CCR4), a chemokine receptor important for T cell migration into the skin, is highly expressed on malignant T‑cells and Tregs in MF and SS [19, 20]. Mogamulizumab is a CCR4-directed, defucosylated, monoclonal antibody that induces antibody dependent cellular cytotoxicity (ADCC) against CCR4+ malignant T cells and Tregs when binding to CCR4 [21]. In 2018 the FDA and the EMA approved mogamulizumab for relapsed or refractory MF and SS that has been pretreated with at least one systemic therapy [22, 23]. The basis of this approval was a phase 3 trial (MAVORIC) involving 372 patients with relapsed or refractory pretreated MF or SS [24]. Patients were stratified by CTCL subtype and clinical stage and were randomly assigned to mogamulizumab in the approved dose of 1.0 mg/kg intravenously once weekly for 4 weeks, followed by further cycles every other week, or to FDA approved vorinostat 400 mg daily. The primary end point was PFS, which was 7.7 months in the mogamulizumab group compared to 3.1 months in the vorinostat group. ORR to mogamulizumab was 28% versus 5% to vorinostat. In SS patients, the response rate to mogamulizumab was higher than in MF patients: 37% versus 21%. Stage dependent response to mogamulizumab was most significant in clinical stage IV: 36% versus 19% in stage IB or IIA. Compartment response was best in blood (68%), followed by skin (42%), lymph nodes (17%) and viscera (0%). The most common AEs of mogamulizumab were infusion related reactions, drug rash, diarrhea and fatigue. Grade 3–4 AEs were reported in 41% of patients, most frequently pyrexia and cellulitis. A total of 19% discontinued treatment due to toxicity. Two treatment-related deaths occurred, one case due to septicemia and another due to polymyositis. Overall, the safety profile was manageable and in accordance with previous reports. In brief, this study underscores the efficacy of mogamulizumab, particularly in SS and advanced stage MF [24]. However, patients with large cell transformation—a histological feature observed in 10–20% of MF/SS patients and associated with poor outcomes [10]—were excluded from this study. A phase 2 study evaluating mogamulizuab in combination with total skin electron beam therapy (TSEBT) in CTCL patients is expected to enroll in May 2020 (MOGAT, NCT04128072) [18].

The approval of BV and mogamulizumab for advanced and refractory MF and SS has broadened the therapeutic spectrum for this incurable disease group with poor prognosis. Lacutamab and PD-1/L‑1 inhibitors have demonstrated encouraging results in phase 1 and phase 2 trials. More promising novel therapeutic agents are currently undergoing clinical trial and will continue to expand the therapeutic options available in the management of advanced-stage MF und SS.