Key PointsQuestion
Is topical synthetic hypericin ointment, 0.25%, activated with visible light an effective and safe photodynamic therapy (PDT) for early-stage mycosis fungoides−cutaneous T-cell lymphoma (MF/CTCL)?
Findings
This multicenter phase 3 randomized clinical trial including 169 patients with MF/CTCLfound that topical hypericin PDT was more effective than placebo after 1 cycle of treatment for 6 weeks (index lesion response rate, 16% vs 4%); responses increased to 40% after 2 cycles, 49% after 3 cycles, and were seen in patch and plaque lesions. Adverse events were primarily mild application-site skin reactions.
Meaning
Topical synthetic hypericin activated with visible light is an effective and well-tolerated PDT for early-stage MF/CTCL.
Importance
Given that mycosis fungoides−cutaneous T-cell lymphoma (MF/CTCL) is chronic, there is a need for additional therapies with minimal short- and long-term adverse effects. Topical synthetic hypericin ointment, 0.25%, activated with visible light is a novel, nonmutagenic photodynamic therapy (PDT).
Objectives
To determine the efficacy and safety of topical synthetic hypericin ointment, 0.25%, activated with visible light as a nonmutagenic PDT in early-stage MF/CTCL.
Design, Settings, and Participants
This was a multicenter, placebo-controlled, double-blinded, phase 3 randomized clinical trial (FLASH study) conducted from December 2015 to November 2020 at 39 academic and community-based US medical centers. Participants were adults (≥18 years) with early-stage (IA-IIA) MF/CTCL.
Interventions
In cycle 1, patients were randomized 2:1 to receive hypericin or placebo to 3 index lesions twice weekly for 6 weeks. In cycle 2, all patients received the active drug for 6 weeks to index lesions. In cycle 3 (optional), both index and additional lesions received active drug for 6 weeks.
Main Outcomes and Measures
The primary end point was index lesion response rate (ILRR), defined as 50% or greater improvement in modified Composite Assessment of Index Lesion Severity (mCAILS) score from baseline after 6 weeks of therapy for cycle 1. For cycles 2 and 3, open label response rates were secondary end points. Adverse events (AEs) were assessed at each treatment visit, after each cycle, and then monthly for 6 months. Data analyses were performed on December 21, 2020.
Results
The study population comprised 169 patients (mean [SD] age, 58.4 [16.0] years; 96 [57.8%] men; 120 [72.3%] White individuals) with early-stage MF/CTCL. After 6 weeks of treatment, hypericin PDT was more effective than placebo (cycle 1 ILRR, 16% vs 4%; P = .04). The ILRR increased to 40% in patients who received 2 cycles of hypericin PDT (P < .001 vs cycle 1 hypericin) and to 49% after 3 cycles (P < .001 vs cycle 1 hypericin). Significant clinical responses were observed in both patch and plaque type lesions and were similar regardless of age, sex, race, stage IA vs IB, time since diagnosis, and number of prior therapies. The most common treatment-related AEs were mild local skin (13.5%-17.3% across cycles 1-3 vs 10.5% for placebo in cycle 1) and application-site reactions (3.2%-6.9% across cycles 1-3 vs 4% for placebo in cycle 1). No drug-related serious AEs occurred.
Conclusion and Relevance
The findings of this randomized clinical trial indicate that synthetic hypericin PDT is effective in early-stage patch and plaque MF/CTCL and has a favorable safety profile.
Trial Registration
ClinicalTrials.gov Identifier: NCT02448381
Mycosis fungoides−cutaneous T-cell lymphoma (MF/CTCL) is a rare non-Hodgkin lymphoma of skin-homing malignant T-cells presenting as patches or plaques in early stages and may progress to tumors, erythroderma, and/or extracutaneous sites in advanced stages.1,2 Early-stage MF/CTCL is treated with primarily skin-directed therapies.2,3 Use of current skin-directed therapies are limited by (1) acute toxic effects (contact dermatitis with topical chemotherapy/retinoids, alopecia with radiation therapy, local inflammation with imiquimod, phototoxic effects of UV light), (2) long-term cumulative toxic effects (skin atrophy with topical corticosteroids, skin cancers with some types of long-term UV phototherapy, alopecia/anhidrosis/fibrosis from radiation therapy), or (3) inadequate efficacy in plaques (vs patches) because of reduced skin penetration. Given MF/CTCL chronicity, short-term tolerability and long-term safety are important treatment considerations supporting an urgent need for additional CTCL skin-directed therapies.
Hypericin, naturally found in plants (Hypericum genus),4-6 is tumoricidal as a stand-alone drug7-12 and with activation by visible light.4,13-20 It is preferentially absorbed into malignant cells, particularly in vivo.7,21 However, in vitro noncancerous cells can also absorb hypericin.8,22,23 Other factors contributing to its tumoritropic attributes are blood flow, vessel permeability, and affinity for interstitial constituents.24 Visible light in the yellow-red spectrum (range, 500-650 nm) is expected to penetrate 1 to 2 mm into the skin20,25 and activates hypericin localized in the perinuclear region within the endoplasmic reticulum and Golgi apparatus.26,27 Activated hypericin triggers the caspase-signaling cascade through reactive oxygen species resulting in apoptosis via the mitochondrial pathway.28 In vitro, hypericin inhibits malignant T-cell proliferation and induces apoptosis in CTCL and adult T-cell leukemia cell lines compared with normal T-cells.29,30 Synthetic hypericin was nonmutagenic in 2 Ames tests and an in vitro cytogenetic assay.
In clinical trials for other indications, systemic hypericin dose-limiting toxicity was phototoxicity, which led to the development of synthetic hypericin ointment (HyBryte) as a topical photodynamic therapy (PDT) activated by noncarcinogenic visible spectrum light. A phase 2 clinical trial of synthetic hypericin PDT demonstrated a statistically significant reduction in early-stage MF/CTCL skin lesions after 6 weeks of treatment (overall response rate, 58.3%; 7 of 12 patients) and was well-tolerated.31 In addition, given its nonmutagenic mechanism of action, hypericin PDT has a potential safety advantage over traditional UV phototherapy for long-term use in patients with MF. We report the efficacy and safety of treatment with hypericin PDT vs placebo in patients with early-stage MF/CTCL in this large placebo-controlled randomized clinical trial.
The FLASH study was a phase 3, placebo-controlled, double-blind, multicenter randomized clinical trial conducted to evaluate the efficacy and safety of synthetic hypericin ointment PDT in patients with early-stage MF/CTCL (stages IA-IIA per international guidelines32). The trial protocol is available in Supplement 1. As agreed with the US Food and Drug Administration (FDA) at the time of the study design, given the lack of consensus of standard first-line skin-directed therapies for early-stage MF/CTCL, a placebo comparator was chosen to better elucidate the drug’s biologic activity, maximize ability to adequately blind treatments, and collect concurrent placebo response data during a reasonable but limited time period. Adults with stage IA-IIA MF/CTCL, and 3 or more evaluable and discrete patch and plaque lesions were enrolled and treated twice weekly during a 6-week cycle for up to 3 cycles (Figure 1): cycle 1, randomized to active drug vs placebo treatment of the 3 prospectively identified index lesions (primary efficacy end point cycle); cycle 2, crossover of patients in the placebo group to receive index-lesion treatment, as well as all cycle 1 patients who received active drug but had not achieved index-lesion complete clinical response in cycle 1; and cycle 3 (optional), open-label treatment of all lesions (index and nonindex) selected by the patient and physician.
The study protocol was approved by each study site’s independent institutional review board in accordance with ethical principles of the Declaration of Helsinki.33 The study was consistent with the International Conference on Harmonization and Good Clinical Practice guidelines and applicable regulatory requirements and in compliance with the protocol. Written informed consent was obtained from all patients before study participation. The study followed the Consolidated Standards of Reporting Trials (CONSORT) reporting guidelines.
Adult patients (≥18 years) with stage IA-IIA MF/CTCL (≥3 patch and/or plaque lesions) were enrolled at 39 academic and community-based US medical centers. Exclusion criteria included use of topical steroids or other skin-directed therapies (eg, nitrogen mustard) on index lesions within 2 weeks of enrollment; treatment with psoralen UV-A or narrow band UV-B phototherapy, topical carmustine, systemic steroids, or other systemic CTCL therapies within 3 weeks; exposure to electron beam irradiation in the treatment field within 3 months; having substantial systemic immunosuppression; experiencing spontaneous improvement in condition; or having advanced MF/CTCL (stage IIB-IV; tumor, erythrodermic). All enrolled cases were confirmed by skin biopsy.
Before randomization, 3 representative index lesions (to include patch and plaque lesions if both present) were identified for treatment and evaluation (Figure 1A). Patients were randomized 2:1 to either hypericin, 0.25%, or placebo ointments (cycle 1 only). Ointment was applied to each index lesion, covered with opaque dressing or clothing for 18 to 24 hours, followed by administration of visible light (range, 500 to 650 nm using an Ultralite Panelite). Light treatment started at 5 joules per cm2 (J/cm2) and increased by 1 J/cm2 with each treatment until a mild skin reaction was seen in treated lesions (grade 1 erythema) or until a maximum light dose of 12 J/cm2 was reached. Index lesions were treated twice weekly for each 6-week cycle. Treatment response was assessed after a 2-week rest period (week 8 for cycle 1, week 16 for cycle 2, and week 24 for cycle 3) to allow treatment-induced skin reactions to subside. Posttreatment outcomes were evaluated in all patients 6 months after the last treatment cycle evaluation visit (at 48 weeks/12 months for those who completed cycle 3).
The primary objective was to evaluate the ability of the initial 6-week course (cycle 1) of hypericin PDT to induce a treatment response, defined as a 50% or more improvement in the cumulative modified Composite Assessment of Index Lesion Severity (mCAILS) score from baseline to the 8-week evaluation visit. The mCAILS score for each index lesion is the sum of the severity subscores of 4 categories: erythema, scaling, plaque elevation, and surface area. Severity was graded from 0 (none) to 8 (severe) for erythema and scaling; 0 to 3 for plaque elevation; and 0 to 18 for surface area.34
A secondary objective evaluated the effect of a second 6-week course of treatment (cycle 2) on index lesions with less than complete response in the initial cycle 1 hypericin PDT and to extend the data on the response rate of hypericin PDT in untreated lesions (after cycle 1, placebo patients crossover). In the optional, open-label portion of the study (cycle 3), the objective was to determine the effect of hypericin PDT treatment with maximal coverage, including assessment of systemic hypericin blood levels. Study investigators were specifically trained on index lesion selection criteria and mCAILS scoring during site initiation visits and when new personnel joined the study. Additionally, the same study investigator was expected to perform all mCAILS scores throughout the study for a given patient to ensure consistency.
The primary efficacy analyses were calculated in the intent-to-treat (ITT) population defined as all randomized patients who received 1 hypericin PDT treatment in each study group. The ITT population was defined for each treatment cycle. Safety analyses were conducted in the same population.
The primary end point for the trial was the proportion of treatment response (defined as ≥50% reduction in total mCAILS score) between the 2 treatment groups at the end of cycle 1. A patient was a responder if the cumulative mCAILS score of the 3 index lesions was 50% or more improvement compared with baseline. Patients with a cumulative mCAILS score of 0 were classified as having a complete clinical response (CR).
The data monitoring committee conducted 1 interim analysis (October 9, 2018), reviewed and locked data from 104 patients who had completed cycle 1 and the week 8 evaluation (primary end point). The interim analysis assessed the primary efficacy end point and key safety end points between treatments in an unblinded manner, and a sample size recalculation was performed. To preserve an overall type I error rate of 0.05, the alpha spending function approach with an O’Brien-Fleming type of stopping rule was used with a 2-sided significance level of α = .001 for the interim analysis and a 2-sided significance level of α = .049 for the final analysis.35 After the interim analysis, the data monitoring committee recommended that enrollment continue to a minimum of 160 evaluable patients.
A prospectively defined logistic regression analysis on treatment response was performed with treatment and baseline total mCAILS score as independent variables. Treatment difference was compared using the Wald test. Data analyses were performed on December 21, 2020, using SAS. version 9.1.3 (SAS Institute).
From 39 sites across the US, 169 patients were randomized into the trial conducted from December 2015 to November 2020; however, 3 of these patients (2 to hypericin; 1 to placebo) did not participate because the investigator decided to change their therapeutic regimen (eFigure 1 in Supplement 2). The study’s ITT population comprised 166 patients (mean [SD] age, 58.4 [16.0] years; 96 [57.8%] men; 70 [42.2%] women; 4 [2.4%] Asian, 39 [23.5%] Black, 120 [72.3%] White, and 3 [1.8%] individuals of other race and ethnicity) who were randomized 2:1 to hypericin PDT (116 participants) or placebo (50 participants) in cycle 1 (2:1). The treatment populations were balanced in terms of demographic information, baseline disease characteristics, and prior therapy (Table 1). Of note, the study included patients relatively naive to treatment as well as those with multiple prior therapies. Patients in both treatment groups received a median of 12 study drug applications (maximum allowed) in cycle 1 (hypericin and placebo) and in both cycles 2 and 3.
After cycle 1 (6-week treatment plus 2-week rest; ie, week 8), the hypericin PDT-treated group had a statistically significant index lesion response rate (ILRR) of 16% (19 of 116 patients) compared with 4% in the placebo-treated group (2 of 50 patients; P = .04). The ILRR increased to 40% for the group that received hypericin PDT in both cycles 1 and 2 (44 of 110 patients vs hypericin PDT group after cycle 1; P < .001). After the optional cycle 3, the ILRR for the group that received hypericin PDT increased further to 49% (38 of 78 patients vs hypericin PDT group after cycle 1 and cycle 2; P = .05; Figure 2A).
Analysis of all patients who received hypericin PDT (ie, including those who received placebo in cycle 1 followed by hypericin PDT in cycle 2) demonstrated a consistent ILRR of 18% after 6 weeks of treatment and 40% after 12 weeks of treatment. The ILRR was similar in patients with MF/CTCL stage IA (42.0%; n = 69) vs stage IB (37.8%; n = 37) and across number of prior treatments (42.4% in patients receiving ≤1 prior treatment; 39.0% for ≥2 prior treatments; Figure 2B) as well as across age, sex, race, and time since MF/CTCL diagnosis. Only 5 patients with MF/CTCL stage IIA enrolled in the trial, and all were randomized to hypericin PDT; 4 of these 5 patients received treatment with a response rate of 25%.
Complete CRs were observed in each cycle (cycle 1, 2 of 166 participants; cycle 2, an additional 7 of 155; cycle 3, additional 6 of 110). All CRs were observed in patients receiving hypericin PDT. Among the 9 patients with CRs during the first 2 cycles, the median (range) age was 56 (20-79) years; 6 (67%) were women; 1 patient was Asian, 4 were Black, and 3 were White; 7 patients had MF/CTCL stage IA and 2 had stage IB; and the median (range) of prior therapies was 2 (0-6) therapies. The improvement in the number of CRs at the end of cycle 2 compared with the end of cycle 1 for those patients receiving hypericin PDT in both cycles (n = 110) was statistically significant (95% CI, 2.0-11.5; P = .03).
Consolidated response rates across all individual index lesions were similar in both patch and plaque lesions (patches identified by mCAILS plaque subscore of 0; plaques identified by mCAILS plaque subscore of 1, 2, or 3; Figure 3). Individual index lesions that achieved a mCAILS score of 0 after at least 6 weeks of hypericin PDT had a median duration of response (elapsed days with 50% of lesions retaining clearance) of 231 days.
Durability of treatment response was improved with increased number of hypericin PDT cycles. A logistic regression model evaluating the duration of treatment response using the number of hypericin PDT cycles and the duration of previous disease as independent variables indicated a statistically significant correlation with the number of treatment cycles (standard error rate, 16.49; P = .01) but not with the previous duration of disease.
Overall across all treatment cycles (hypericin and placebo), treatment-emergent AEs of any causality (ie, any/all AEs that occurred during the entire study period regardless of relationship to study intervention) were reported in 70% of patients (116 of 166) and were similar in both treatment groups during cycle 1 with the exception of slightly more treatment-site AEs seen with hypericin PDT: skin reactions (16.4% hypericin PDT vs 10.5% placebo), pruritus (cycle 1, 5.2% hypericin PDT vs 4.0% placebo), application-site pain and/or irritation (cycle 1, 6.9% hypericin PDT vs 4.0% placebo), application-site pruritus (cycle 1, 4.3% hypericin PDT vs 2.0% placebo) that in some cases mildly increased with more prolonged treatment with hypericin PDT during cycles 2 and 3 (Table 2).
Mild treatment-related AEs were reported in 23% (n = 38) of patients, moderate in 9% (n = 15), and severe in 3 (2%). Most of the AEs that were possibly related (11%) or related (15% ) to hypericin PDT were skin reactions including pruritus, hyperpigmentation, burning, pain, and irritation, and application-site pain and pruritus. The majority of these were mild, required no intervention or treatment, and did not interfere with continued treatment and study participation. During cycle 1, the study discontinuation rate was 5% of the hypericin PDT group and 10% of the placebo group. All patients who received hypericin PDT during cycles 1 through 3 had a study discontinuation rate during the treatment cycles of 5.0%, with only 1.2% being AE related.
A severe treatment-related AE occurred in 3 patients. One patient had application-site pain in cycle 3; it required no intervention and resolved. Another patient experienced erythema in cycle 1; it resolved after a pause in treatment, and treatment was resumed without issue. The third was a patient with application-site pain during cycle 1; the participant withdrew from the study.
There were 5 serious adverse events (SAEs) during the study, but all were considered unrelated to hypericin PDT; 4 were related to underlying medical conditions or medications unrelated to MF/CTCL. There were no deaths during the study. There were no clinically meaningful changes in any hematologic or clinical chemistry parameters, nor any trending changes in vital signs among the study participants. Systemic hypericin blood concentration was measured in 29 patients, sampled 24 hours after ointment application across the last 4 treatments in cycle 3 (time point of maximum exposure). No hypericin was detected in the blood using a validated method with a detection limit of 5 ng/mL.
This double-blind, placebo-controlled phase 3 randomized clinical trial demonstrated that hypericin PDT is an effective and well-tolerated treatment for early-stage MF/CTCL. Hypericin PDT resulted in a significant improvement in ILRR compared with placebo in cycle 1 with continued improvement in cycle 2 and in optional cycle 3. A significantly greater proportion of patients treated with hypericin PDT had experienced CR after cycle 2. Importantly, treatment benefit was similar in patch and plaque lesions, suggesting enhanced depth of penetration with visible light spectrum wavelengths (eFigure 2 in Supplement 2), which would be an advantage over some current MF/CTCL skin-directed therapies. Notably, the treatment response rate of hypericin PDT in cycle 1 (16%) was considerably lower than previously observed in the prior phase 2 trial (58.3%) but still statistically significant compared with placebo treatment. One important consideration is the prior trial used different end point criteria to assess treatment response (reduction in lesion size) rather than the multifaceted mCAILS score used in this trial (ie, incorporating erythema, scaling, and thickness, as well as lesion size). The mCAILS score is the standard skin assessment tool for individual lesion clinical response assessment. It is recommended for all early-stage MF/CTCL clinical trials and endorsed by US and international MF/CTCL specialty group consensus publications.36
Hypericin PDT showed no evidence of systemic absorption and had an acceptable safety profile with possibly related or related AEs that were limited to pruritus, hyperpigmentation, burning, pain, irritation, and application-site pain and/or pruritus; all were self-limited. Having a variety of treatment options is critical for managing early-stage MF/CTCL. In addition to efficacy, other factors such as patient comorbidities, access, and AEs affect treatment selection. Hypericin PDT has a similar treatment schedule to traditional UV phototherapy but is more targeted to skin surface area and requires a light panel in the 500 to 650 nm spectrum that is potentially safer in patients with severe actinic skin damage and skin cancer history. Because hypericin PDT requires occlusion 12 to 24 hours after hypericin application, its use may be limited in certain anatomic sites (face), although site application limitations exist for all other current MF/CTCL skin-directed therapies (eg, topical chemotherapy not used in body folds or the central face).
Future directions include assessing clinical response and AEs with continuous hypericin PDT treatment without the 2-week rest periods and for longer periods to reflect real-world practice. Hypericin PDT is also potentially suited for administration with an at-home light unit and could be a valuable user-friendly option to improve access to treatment for patients who live far from a health care center and/or prefer the shift away from in-office treatments that occurred during the COVID-19 pandemic.
Limitations of the study included incomplete information correlating clinical response with (1) skin pigmentation (Fitzpatrick scale), although no difference in response was observed across race; (2) clinical or histologic subtypes of MF/CTCL (eg, folliculotropic); (3) presence or absence of large-cell transformation because these were not required data for study entry, although folliculotropism or large-cell transformation were not specifically excluded.
Another study limitation was the short duration of treatment for each cycle (6-week treatment, 2-week rest before response assessment) and overall treatment period (maximum 6 months) which differs from real-world skin-directed treatment courses. However, during the trial design, placebo treatment of more than 8 weeks was considered unacceptable in patients with active MF/CTCL, thus a crossover design was used for cycle 2—patients initially randomized to placebo in cycle 1 could receive active treatment thereafter. These second and third cycles in which all patients received hypericin PDT allowed safety and efficacy assessments to be conducted during a longer treatment period. Outcomes at these later time points (ILRR, 40% and 49% at wk 16 and 24) demonstrated clinical response kinetics that were comparable to other MF/CTCL skin-directed therapies studied during longer clinical trial periods (eg, bexarotene gel, mechlorethamine gel).37-39 To date, all FDA-approved MF/CTCL therapies are indicated for disease refractory to previous MF/CTCL therapy. As demonstrated in Figure 2, hypericin PDT efficacy was similar irrespective of disease stage or refractory status (eg, ≥2 prior MF/CTCL therapies).
The FLASH randomized clinical trial demonstrated that hypericin PDT is a clinical advance for the field with its comparable efficacy in patch and plaque lesions and favorable short-term and, potentially, long-term safety profile. Given that MF/CTCL requires long-term disease management and that many patients using current skin-directed therapies experience short- and/or long-term adverse effects, limited access, and waning efficacy, these findings are an important contribution to MF/CTCL patient care.
Accepted for Publication: May 19, 2022.
Published Online: July 20, 2022. doi:10.1001/jamadermatol.2022.2749
Corresponding Authors: Ellen J. Kim, MD, Department of Dermatology, Perelman School of Medicine at the University of Pennsylvania, 3400 Civic Center Blvd, Philadelphia, PA 19104 (ellen.kim@pennmedicine.upenn.edu); and Brian Poligone, MD, PhD, Rochester Skin Lymphoma Medical Group, 6800 Pittsford Palmyra Rd, Fairport, NY 14450 (bpoligone@roclymphoma.com).
Author Contributions: Dr E. Kim had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Drs E. Kim and Poligone are equally responsible for correspondence regarding the study.
Concept and design: Bhatia, Musiek, Elston, Duvic, Lee, Girardi, Rumage, Donini, Haulenbeek, Schaber, Straube, Pullion, Rook, Poligone.
Acquisition, analysis, or interpretation of data: E. Kim, Mangold, DeSimone, Wong, Seminario-Vidal, Guitart, Appel, Geskin, Lain, Korman, Zeitouni, Nikbakht, Dawes, Akilov, Carter, Shinohara, Kuzel, Piette, Pariser, Y. Kim, Elston, Boh, Duvic, Huen, Pacheco, Zwerner, Girardi, Querfeld, Bohjanen, Olsen, Wood, Rumage, Donini, Haulenbeek, Schaber, Straube, Poligone.
Drafting of the manuscript: E. Kim, Mangold, Akilov, Bhatia, Elston, Donini, Straube, Pullion, Poligone.
Critical revision of the manuscript for important intellectual content: E. Kim, Mangold, DeSimone, Wong, Seminario-Vidal, Guitart, Appel, Geskin, Lain, Korman, Zeitouni, Nikbakht, Dawes, Akilov, Carter, Shinohara, Kuzel, Piette, Musiek, Pariser, Y. Kim, Boh, Duvic, Huen, Pacheco, Zwerner, Lee, Girardi, Querfeld, Bohjanen, Olsen, Wood, Rumage, Donini, Haulenbeek, Schaber, Straube, Rook, Poligone.
Statistical analysis: Bhatia, Elston, Haulenbeek, Straube.
Obtained funding: Boh, Schaber.
Administrative, technical, or material support: Mangold, Seminario-Vidal, Geskin, Nikbakht, Boh, Duvic, Huen, Querfeld, Wood, Rumage, Donini, Haulenbeek, Schaber, Straube, Pullion, Rook, Poligone.
Supervision: E. Kim, Guitart, Geskin, Musiek, Y. Kim, Duvic, Lee, Girardi, Rumage, Donini, Haulenbeek, Schaber, Straube, Pullion, Poligone.
Other—Trial investigator: Huen.
Other—Co-inventor on patent: Schaber.
Other—Olsen.
Other—Clinical trial accrual: Kuzel.
Other—Patient screening and enrolment, institutional data management: Querfeld.
Conflict of Interest Disclosures: Dr E. Kim reported grants from Innate Pharma and Galderma; consulting/advisory fees from Almirall, Galderma, and Helsinn; and honoraria from Ology and UpToDate, all outside the submitted work. Dr Mangold reported grants from Crispr Therapeutics, Elorac, Kyowa Hakko Kirin, and Sun Pharmaceuticals; consulting/advisory fees from UCB, Eli Lilly, Regeneron, PHLEC, Corbus, Incyte, Pfizer, Novartis, Jansen, Argenx, Akari, and Castle Biosciences, all outside the submitted work. Dr Seminario-Vidal reported grants from Kyowa Kirin, and personal fees from Kyowa Kirin, Novartis, Boehringer Ingelheim, Helsinn, Regeneron, Blueprint, Eli Lilly, Soligenix, Helsinn, Eisai, AbbVie, Bristol Myers Squibb, Celgene, Glenmark, Amgen, AnaptysBio, and Innate Pharma outside the submitted work; and being a faculty member at the University of South Florida during the conduct of the study. Dr Guitart reported personal fees from Kirin Kyowa and Elorac outside the submitted work. Dr Korman reported consulting and advisory fees from AbbVie, Amgen, Argenx, Boehringer Ingelheim, Bristol Myers Squibb, Celgene, ChemoCentryx, Dermavant, Dermira, Eli Lilly, Galderma, Genentech, GlaxoSmithKline, Immune, Janssen, Kyowa Hakko Kirin Pharma, Leo Pharma, Menlo Therapeutics, Novartis, Pfizer, Principia, Prothena, Regeneron, Rhizen, Soligenix, Sun Pharma, Syntimmune, Trevi Therapeutics, UCB, Valeant, and XBiotech, outside the submitted work. Dr Zeitouni reported grants from Sun Pharma, Biofrontera, and speaking honoraria from Biofrontera outside the submitted work. Dr Nikbakht reported consulting fees and serving as a member of Helsinn Advisory Board. Dr Shinohara reported grants from Elorac, Cabaletta Bio, and Astex, and serving on the board of the US Cutaneous Lymphoma Consortium outside the submitted work. Dr Piette reported a grant through Rush Medical University from Soligenix outside the submitted work. Dr Kuzel reported grants from Eisai and speaker’s honoraria from Kyowa Kirin. Dr Musiek reported personal fees and grants from Kyowa, Elorac, UpToDate, ADD Board Prep Plus Author, Pfizer, Bristol Myers Squibb, and Aristea Therapeutics, all outside the submitted work. Dr Pariser reported consulting fees from Biofrontera, Dermira, Novartis, Regeneron, Bickel Biotechnology, and Sanofi; and serving as a DSMB member of Bristol Myers Squibb, on the advisory board for Pfizer, and a researcher for Almirall, Amgen, AOBiome, Asana Biosciences, Bickel Biotech, Celgene, Dermira, Eli Lilly, Leo Pharma, Menlo Therapeutics, Novartis, Novo Nordisk, Ortho Dermatologics, Pfizer, and Regeneron, all outside the submitted work. Dr Olsen reports receiving consulting fees from Kyowa Kirin, UpToDate, Molecular Biotech, Helsinn, Soligenix and served on data safety monitoring board for Affimed. Dr Boh reported grants through the Tulane School of Medicine during the conduct of the study. Dr Duvic reported serving on the Soligenix scientific advisory board during the conduct of the study; and personal fees from Eisai, Bionz Consulting, and Bausch scientific advisory board outside the submitted work. Dr Huen reported grants from Kyowa Kirin, Trillium, Galderma, Innate, Eisai, and Seattle Genetics; and personal fees from Kyowa Kirin, Rhizen, Stemline, Helsinn, all outside the submitted work. Dr Querfeld reported advisory board fees from Helsinn, Kyowa Kirin, Mallinckrodt, Stemline, Helsinn, Celgene, and speaking fees from Helsinn, all outside the submitted work. Dr Wood reported serving on the scientific advisory board of Soligenix. Dr Rumage reported equity in Soligenix and a grant from the US National Cancer Institute (NCI), outside the submitted work. Dr Schaber reported a grant from NCI during the conduct of the study and being the co-investor and holding a patent for the hypericin process. Dr Straube reported a grant from NCI during the conduct of the study. Dr Pullion reported personal fees from Soligenix outside the submitted work. Dr Rook reported serving on the scientific advisory board of Soligenix and speaking fees from Mallinckrodt. No other disclosures were reported.
Funding/Support: The research was sponsored and funded by Soligenix Inc.
Role of the Funder/Sponsor: The sponsor participated in the conception and design of the study, analysis, and interpretation of the data, drafting and critical revision of the report and gave approval to submit the manuscript for publication.
Additional Contributions: Medical writing and editorial assistance was provided by Kathryn Martin, PharmD (Glenmere Research); there was no financial compensation outside of salary.
Data Sharing Statement: See Supplement 3.
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