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Phase I trial of subcutaneous recombinant human interleukin-2 in patients with metastatic melanoma

โœ Scribed by Omar Eton; Michael G. Rosenblum; Sewa S. Legha; Wehei Zhang; Mary Jo East; Agop Bedikian; Nicholas Papadopoulos; Antonio Buzaid; Robert S. Benjamin


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
91 KB
Volume
95
Category
Article
ISSN
0008-543X

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โœฆ Synopsis


Abstract

BACKGROUND

Interleukinโ€2 (ILโ€2) has activity in metastatic melanoma when given in high doses by the intravenous (IV) route, but its side effects and effectiveness when given in intermediate to high doses by the subcutaneous (SC) route have not been studied adequately. This study sought to determine the maximum tolerated dose (MTD) of ILโ€2 administered once daily by the SC route.

METHODS

Outpatients with progressive metastatic melanoma after chemotherapy were enrolled in a Phase I trial of ILโ€2 administered SC daily for 5 days per week for 4 consecutive weeks, repeated at 6โ€week intervals. Patients were instructed to drink at least 2 L of fluid daily. ILโ€2 pharmacokinetic studies were performed at the two highest dose levels. Toxicity was recorded weekly using the National Cancer Institute Common Toxicity Criteria. Response was assessed at 6โ€week intervals.

RESULTS

Three patients, 6 patients, 6 patients, and 4 patients received a median of 2 courses of SC ILโ€2 at dose levels of 6 MIU/m^2^, 9 MIU/m^2^, 12 MIU/m^2^, and 15 MIU/m^2^, respectively. Failure to maintain adequate fluid intake was responsible for 2 episodes of syncope at the 9 MIU/m^2^ dose level and for 2 incidents of reversible prerenal azotemia at the 15 MIU/m^2^ dose level. ILโ€2 treatment was resumed in these patients without incident. At the 15 MIU/m^2^ dose level, 2 patients had severe headaches, depression, and visual hallucinations requiring discontinuation of treatment. Cough and fluid retention at the end of the third and fourth weeks at the 15 MIU/m^2^ dose level approximated the symptoms reported by inpatients treated by continuous IV infusion at 9 MIU/m^2^ on the same schedule. There was a partial response and a complete response in subcutaneous disease at the 12 MIU/m^2^ and 15 MIU/m^2^ dose levels, respectively, each lasting < 2 months. Plasma ILโ€2 levels after SC injection of 1000โ€“5000 pg/mL reached maximum by 3 hours and were detectable for up to 48 hours after administration. The halfโ€lives for SC ILโ€2 absorbance and clearance were 1.6 hours and 5.2 hours, respectively, and the calculated area under the curve was 30,584 pg/mL ร— hour.

CONCLUSIONS

SC ILโ€2 was well tolerated and had high sustained bioavailability at the higher doses studied. The MTD for a daily SC regimen was 12 MIU/m^2^ and is recommended for future studies. Cancer 2002;95:127โ€“34. ยฉ 2002 American Cancer Society.

DOI 10.1002/cncr.10631


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