2012
DOI: 10.1016/j.biopha.2012.03.005
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Thalidomide for improving cutaneous and pulmonary sarcoidosis in patients resistant or with contraindications to corticosteroids

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Cited by 36 publications
(13 citation statements)
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“…178 Despite this disappointing outcome, it is possible that more prolonged and/or higher doses of thalidomide may achieve better results, particularly since a non-controlled study with less precise methodology found that the percentage of complete responses induced by thalidomide in the subjects with cutaneous sarcoidosis rose from 32% at 3 months to 67% at 6 months, respectively. 160 Notably, in the open-label follow up trial conducted at the conclusion of the prospective 3 month Droitcourt study, 11 of 14 patients who remained on thalidomide for 6 months as well as 10 of 14 receiving placebo improved or very well improved, suggesting the possible benefit of time. Besides concern about teratogenicity and neuropathy, major drawbacks are the need to enroll in a restricted program under the Thalidomide Risk Evaluation and Mitigation Strategy program and reluctance for insurance to cover because the drug does not have regulatory approval for sarcoidosis.…”
Section: Tumor Necrosis Factor Alpha Inhibitorsmentioning
confidence: 96%
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“…178 Despite this disappointing outcome, it is possible that more prolonged and/or higher doses of thalidomide may achieve better results, particularly since a non-controlled study with less precise methodology found that the percentage of complete responses induced by thalidomide in the subjects with cutaneous sarcoidosis rose from 32% at 3 months to 67% at 6 months, respectively. 160 Notably, in the open-label follow up trial conducted at the conclusion of the prospective 3 month Droitcourt study, 11 of 14 patients who remained on thalidomide for 6 months as well as 10 of 14 receiving placebo improved or very well improved, suggesting the possible benefit of time. Besides concern about teratogenicity and neuropathy, major drawbacks are the need to enroll in a restricted program under the Thalidomide Risk Evaluation and Mitigation Strategy program and reluctance for insurance to cover because the drug does not have regulatory approval for sarcoidosis.…”
Section: Tumor Necrosis Factor Alpha Inhibitorsmentioning
confidence: 96%
“…[157][158][159][160]177 Often, responders relapse after thalidomide discontinuation. 159,160 A more recently published, multicenter, randomized, double-blind, placebo-controlled investigatormasked study that included an intent-to-treat population of 39 subjects with clinical and biopsy confirmed cutaneous sarcoidosis did not achieve complete responses after 3 months of thalidomide at a dose of 100 mg daily and, similarly to the control group, 21% had partial responses.…”
Section: Tumor Necrosis Factor Alpha Inhibitorsmentioning
confidence: 99%
“…[160][161][162][163][164] Because of its side effect profile, including teratogenicity, neuropathy, and venous thrombosis, it often is reserved for recalcitrant or severe skin disease. A recent double-blind placebo-controlled trial failed to show efficacy in patients with severe cutaneous disease.…”
Section: Differential Diagnosismentioning
confidence: 99%
“…This response was attributed to macrophage inhibition. No benefit attributed in treatment of Pulmonary Sarcoidosis [13].…”
Section: Sarcoidosismentioning
confidence: 99%