This Article Full Text Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Rosen, L. S. Articles by Brown, G. L. Search for Related Content PubMed PubMed Citation Articles by Rosen, L. S. Articles by Brown, G. L.

Phase 1 Study of TLK286 (Telcyta) Administered Weekly in Advanced Malignancies

¹ Jonsson Comprehensive Cancer Center, University of California, Los Angeles, and ² Telik, Inc., Palo Alto, California

Purpose: To determine the dose-limiting toxicities, maximum tolerated dose, and pharmacokinetics of TLK286, a novel cancer prodrug, administered weekly.

Patients and Methods: Patients with advanced malignancies were treated with TLK286 administered weekly by i.v. infusion over 30 min in escalating doses 60–960 mg/m². A treatment cycle was defined as 3 weekly treatments. Patients underwent tumor assessments on day 43, and those patients receiving clinical benefit continued on treatment until disease progression or unacceptable toxicity. Safety was assessed by the WHO criteria.

Results: Thirty-seven patients received 111 cycles of TLK286 at eight dose levels (median, 3 cycles; range, 1–16 cycles). In this study, TLK286 given weekly at 960 mg/m² was well tolerated without dose-limiting toxicities. TLK286-related toxicities included grade 1–2 nausea and vomiting, fatigue and anemia. Nine of 31 evaluable patients continued therapy beyond day 43 and received a median of 5 cycles (range of 3–16 cycles) and experienced durable stable disease or minor tumor regression. Pharmacokinetic characteristics of TLK286 are described by an optimized two-compartment model. Mild to moderate renal or hepatic organ dysfunction did not impact the elimination of TLK286.

Conclusions: TLK286 administered weekly at doses up to 960 mg/m² were well tolerated. The safety and antitumor activity observed in a broad range of cancer types supports Phase 2 disease-specific investigations of TLK286 given weekly at 960 mg/m².