Background: MKT 077 is a rhodacyanine dye analogue which preferentially accumulates in tumour cell mitochondria. It is cytotoxic to a range of tumours. In this phase I study, MKT 077 was administered as a five-day infusion once every three weeks. Patients and methods: Ten patients, median age 59 (38-70) years, with advanced solid cancers were treated at three dose levels: 30, 40 and 50 mg/m2/day for a total of 18 cycles. 31Phosphorus magnetic resonance spectroscopy (MRS) was used to evaluate the effect of MKT077 on skeletal muscle mitochondrial function. Results: The predominant toxicity was recurrent reversible functional renal impairment (grade 2, two patients). One patient with renal cancer attained stable disease and the remainder progressive disease. There were no MRS changes in the first or second treatment cycles but one patient received 11 treatment cycles and developed changes consistent with a mitochondrial myopathy. Mean values for all pharmacokinetic parameters were at sub micromolar levels and did not exceed IC50 values (>1 uM). Conclusions: Because of the renal toxicity, and animal studies showing MKT 077 causes eventual irreversible renal toxicity, further recruitment was halted. The study shows, however, that it is feasible to target mitochondria with rhodacyanine analogues, if drugs with higher therapeutic indices could be developed.

Phase I trial of the selective mitochondrial toxin MKT 077 in chemo-resistant solid tumours / D.J. Propper; J.P. Braybrooke; D.J. Taylor; R. Lodi; P. Styles; J.A. Cramer; W.C.J. Collins; N.C. Levitt; D.C. Talbot; T.S. Ganesan; A.L. Harris. - In: ANNALS OF ONCOLOGY. - ISSN 0923-7534. - STAMPA. - 10:(1999), pp. 923-927. [10.1023/a:1008336904585]

Phase I trial of the selective mitochondrial toxin MKT 077 in chemo-resistant solid tumours

R. Lodi;
1999

Abstract

Background: MKT 077 is a rhodacyanine dye analogue which preferentially accumulates in tumour cell mitochondria. It is cytotoxic to a range of tumours. In this phase I study, MKT 077 was administered as a five-day infusion once every three weeks. Patients and methods: Ten patients, median age 59 (38-70) years, with advanced solid cancers were treated at three dose levels: 30, 40 and 50 mg/m2/day for a total of 18 cycles. 31Phosphorus magnetic resonance spectroscopy (MRS) was used to evaluate the effect of MKT077 on skeletal muscle mitochondrial function. Results: The predominant toxicity was recurrent reversible functional renal impairment (grade 2, two patients). One patient with renal cancer attained stable disease and the remainder progressive disease. There were no MRS changes in the first or second treatment cycles but one patient received 11 treatment cycles and developed changes consistent with a mitochondrial myopathy. Mean values for all pharmacokinetic parameters were at sub micromolar levels and did not exceed IC50 values (>1 uM). Conclusions: Because of the renal toxicity, and animal studies showing MKT 077 causes eventual irreversible renal toxicity, further recruitment was halted. The study shows, however, that it is feasible to target mitochondria with rhodacyanine analogues, if drugs with higher therapeutic indices could be developed.
1999
Phase I trial of the selective mitochondrial toxin MKT 077 in chemo-resistant solid tumours / D.J. Propper; J.P. Braybrooke; D.J. Taylor; R. Lodi; P. Styles; J.A. Cramer; W.C.J. Collins; N.C. Levitt; D.C. Talbot; T.S. Ganesan; A.L. Harris. - In: ANNALS OF ONCOLOGY. - ISSN 0923-7534. - STAMPA. - 10:(1999), pp. 923-927. [10.1023/a:1008336904585]
D.J. Propper; J.P. Braybrooke; D.J. Taylor; R. Lodi; P. Styles; J.A. Cramer; W.C.J. Collins; N.C. Levitt; D.C. Talbot; T.S. Ganesan; A.L. Harris
File in questo prodotto:
Eventuali allegati, non sono esposti

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/902809
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 106
  • ???jsp.display-item.citation.isi??? 102
social impact