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← Mycosis Fungoides and Other Cutaneous T-Cell Lymphomas

HEALTH PROFESSIONAL · SOURCE READING

Photodynamic therapy

Source: Mycosis Fungoides and Other Cutaneous T-Cell Lymphomas Treatment (PDQ®)–Health Professional Version, National Cancer Institute.

Source updated: February 19, 2025 · Captured 2026-09-09.

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Context: Treatment of Recurrent Mycosis Fungoides and Sézary Syndrome / Treatment Options for Recurrent Mycosis Fungoides and Sézary Syndrome

PUVA radiation therapy.[11-16]

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PUVA radiation therapy.[11-16]

Therapeutic trials with PUVA have shown an 80% to 90% complete remission rate in patients, with those in early cutaneous stages achieving the best responses. PUVA may be used in conjunction with systemic treatment.[15] Continued maintenance therapy with PUVA at more protracted intervals is generally required to prolong remission duration.[11-13,15] PUVA combined with interferon alfa-2a is associated with a high response rate.[14,15]

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Narrowband ultraviolet B radiation.[17,18]

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Narrowband ultraviolet B radiation.[17,18]

Single-arm and retrospective comparisons confirm the efficacy of narrowband ultraviolet B with 80% to 90% complete remission rates, especially for patients with early cutaneous stages.[17,18]

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Narrowband ultraviolet B radiation.[17,18]

A Cochrane systematic review and meta-analysis compared PUVA with narrowband ultraviolet B radiation in 778 patients with early-stage mycosis fungoides (stage IA, IB, and IIA). Significantly higher complete response rates were seen in patients treated with PUVA (73.8% vs. 62.2%; hazard ratio [HR], 1.68; 95% confidence interval [CI], 1.02–2.76; P = .04). There were no significant differences in adverse effects.[16][Level of evidence B3]

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Extracorporeal photophoresis (ECP) has produced tumor regression in patients who are resistant to other therapies.[19,20]

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Extracorporeal photophoresis (ECP) has produced tumor regression in patients who are resistant to other therapies.[19,20]

In a retrospective analysis of 65 patients, with a median follow-up of 48 months, use of ECP in the first to third line of treatment yielded a longer median time-to-next treatment (TTNT) than other systemic options (P < .03).[21][Level of evidence C3]

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Preserved source evidence · Not medical advice