The Effects of Treatment with Interleukin-1 Alpha on Platelet Recovery After High-dose Carboplatin
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Background: Thrombocytopenia is a frequent side effect of cancer chemotherapy and commonly limits attempts to escalate drug doses. To determine whether interleukin-1 alpha could ameliorate carboplatin-induced thrombocytopenia, we combined it with high-dose carboplatin in 43 patients with advanced neoplasms.
Methods: High-dose carboplatin (800 mg per square meter of body-surface area) was administered alone to a control group. Subsequent patients were randomly assigned to receive the same dose of carboplatin with interleukin-1 alpha, administered either before or after carboplatin. Interleukin-1 alpha was given intravenously at a dose of 0.03, 0.1, or 0.3 microgram per kilogram of body weight per day for five days.
Results: Carboplatin alone consistently produced thrombocytopenia with a median nadir of 19,000 platelets per cubic millimeter and a median of 10 days with less than 100,000 platelets per cubic millimeter. All 15 patients receiving interleukin-1 alpha before carboplatin had similar findings. In contrast, 5 of the 15 patients given one of the two higher doses of interleukin-1 alpha after carboplatin had minimal thrombocytopenia (nadir, 91,000 to 332,000 platelets per cubic millimeter). In the 10 patients given 0.3 microgram of interleukin-1 alpha per kilogram after carboplatin treatment, the platelet count recovered to 100,000 per cubic millimeter significantly earlier than in either the control group (P = 0.002) or the patients who received interleukin-1 alpha before carboplatin (P = 0.003), with the median times to recovery in the three groups being 16, 21, and 23 days, respectively. At the highest dose of interleukin-1 alpha, toxicity was substantial (but reversible), requiring inpatient support for hypotension, supraventricular arrhythmias, and pulmonary-capillary leak.
Conclusions: Interleukin-1 alpha can accelerate the recovery of platelets after high-dose carboplatin therapy and may be clinically useful in preventing or treating thrombocytopenia induced by chemotherapy.
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Malireddi R, Bynigeri R, Kancharana B, Sharma B, Burton A, Pelletier S Front Immunol. 2022; 13:1068230.
PMID: 36505497 PMC: 9729281. DOI: 10.3389/fimmu.2022.1068230.
Treatment of Inflammatory Diseases with IL-1 Blockade.
Dinarello C Curr Otorhinolaryngol Rep. 2020; 6(1):1-14.
PMID: 33133777 PMC: 7597638. DOI: 10.1007/s40136-018-0181-9.
Jeong G, Lee K, Lee I, Oh J, Kim D, Shin J J Clin Med. 2019; 8(2).
PMID: 30691103 PMC: 6406478. DOI: 10.3390/jcm8020143.
Ding S, Wang M, Fang S, Xu H, Fan H, Tian Y Front Pharmacol. 2018; 9:297.
PMID: 29666579 PMC: 5891617. DOI: 10.3389/fphar.2018.00297.