Prospective Prediction of Plasma Pharmacokinetics of a Novel Immune-modulating Agent in Cancer Patients after Intra-tumoral Administration: Translation from Non-clinical Species to Humans

Xenobiotica ◽  
2021 ◽  
pp. 1-30
Author(s):  
Ragini Vuppugalla ◽  
Ramola Sane ◽  
Michael Wichroski ◽  
Ashvini Kumar Gavai ◽  
Sarandeep Boyanapalli ◽  
...  
2013 ◽  
Vol 36 (4) ◽  
pp. 676-681 ◽  
Author(s):  
Shinya Motohashi ◽  
Yasuaki Mino ◽  
Katsuhito Hori ◽  
Takafumi Naito ◽  
Seiji Hosokawa ◽  
...  

Pain ◽  
1987 ◽  
Vol 30 (3) ◽  
pp. 339-348 ◽  
Author(s):  
Raymond F. Greene ◽  
Angela W. Miser ◽  
Cindy M. Lester ◽  
Frank M. Balis ◽  
David G. Poplack

2014 ◽  
Vol 32 (3_suppl) ◽  
pp. 578-578 ◽  
Author(s):  
Catherine HyeWon Han ◽  
Prashannata Khwaounjoo ◽  
Dean H. Kilfoyle ◽  
Andrew Graham Hill ◽  
Mark James McKeage

578 Background: Calcium and magnesium (Ca/Mg) infusions have been suggested as an effective intervention for preventing oxaliplatin-induced neurotoxicity, but the effects of Ca/Mg infusions on oxaliplatin pharmacokinetics, motor nerve hyperexcitability, and acute neurotoxicity symptoms are unclear. Methods: In this double-blind crossover study, colorectal cancer patients undergoing oxaliplatin-based chemotherapy were randomised to receive Ca/Mg (1g Ca Gluconate plus 1g MgSO4) on cycle 1 and placebo (vehicle alone) on cycle 2, or to receive the same treatments in the opposite sequence. Study endpoints included plasma pharmacokinetics of intact oxaliplatin and free platinum; electromyography (EMG) detection of abnormal spontaneous high-frequency motor unit action potential discharges; and patient-reported acute neurotoxicity symptoms and their preferred study treatment for reducing these symptoms. Results: The planned accrual target was achieved. Nineteen of 20 enrolled patients completed the study. Plasma pharmacokinetics of intact oxaliplatin and free platinum were similar when oxaliplatin was given with Ca/Mg or placebo (ratio of geometric means of AUC0-t with Ca/Mg or placebo: intact oxaliplatin, 0.95 (90% CI, 0.90 – 1.01); free platinum, 0.99 (90% CI, 0.94 – 1.05)). EMG motor nerve hyperexcitability scores were similar with Ca/Mg and placebo (mean difference in EMG score between Ca/Mg and placebo: -0.3 (95% CI, -2.2 – 1.6)). Patient-reported acute neurotoxicity symptoms were similar in frequency with Ca/Mg and placebo. For reducing neurotoxic symptoms, fewer patients preferred Ca/Mg than placebo or neither treatment (26% versus 74%; p < 0.01). Conclusions: Ca/Mg infusions do not alter the clinical pharmacokinetics of oxaliplatin and do not seem to reduce its acute neurotoxicity. Clinical trial information: ACTRN12611000738921.


1996 ◽  
Vol 14 (3) ◽  
pp. 729-736 ◽  
Author(s):  
A Falcone ◽  
R Danesi ◽  
F Dargenio ◽  
E Pfanner ◽  
I Brunetti ◽  
...  

PURPOSE To determine the plasma pharmacokinetics and the maximum-tolerated dose (MTD) of intravenous (IV) azidothymidine (AZT) administered 90 to 120 minutes after fluorouracil (5-FU) and leucovorin and to preliminarily evaluate the antitumor activity of this combination in metastatic colorectal cancer. PATIENTS AND METHODS 5-FU 500 mg/m2 IV bolus was administered once a week in the middle of a 2-hour infusion of leucovorin; AZT was given as a 90 to 120-minute IV infusion 60 minutes after 5-FU. Initial AZT dose was 0.5 g/m2, and it was escalated in successive cohorts of three patients by 0.5 to 2 g/m2. RESULTS Thirty-five chemotherapy-naive metastatic colorectal cancer patients were entered onto the study, and AZT doses ranged from 0.5 to 10 g/m2. The peak AZT plasma concentration increased from 21.9 to 995.6 micromol/L. The area under the concentration/time curve (AUC) also showed a progressive, but not linear increase from 40.34 to 3,108 h x micromol/L. The most relevant toxicity was diarrhea, which was severe in six patients (17%). Toxicities were not AZT-dose-related, except fpr hypotension, which occurred in patients treated at AZT doses > or = 7 g/m2 and became dose-limiting for AZT 10 g/m2. Among 34 assessable patients, 15 objective responses were observed (44%; 95% confidence interval 27 to 62), lasting a median of 44 weeks; five (15%) were complete. CONCLUSION AZT doses > or = 6 g/m2 administered IV over 90 to 120 minutes produce maximum plasma concentration and AUC similar to those previously reached in murine tumor models. Dose-limiting toxicity is hypotension, which occurs at AZT 10 g/m2. The recommended AZT dose for further studies is 8 g/m2. The combination of 5-FU plus leucovorin plus AZT is feasible with acceptable toxicities, and has promising activity in metastatic colorectal cancer.


1994 ◽  
Vol 16 (2) ◽  
pp. 167
Author(s):  
W. B. Webster ◽  
S. J. Harwood ◽  
R. G. Carroll ◽  
M. A. Morrissey ◽  
J. U. Patel ◽  
...  

1988 ◽  
Vol 22 (1) ◽  
Author(s):  
M. Zucchetti ◽  
M. D'Incalci ◽  
Y. Willems ◽  
F. Cavalli ◽  
C. Sessa

2005 ◽  
Vol 23 (6) ◽  
pp. 1070-1077 ◽  
Author(s):  
Albert J. ten Tije ◽  
Jaap Verweij ◽  
Michael A. Carducci ◽  
Wilfried Graveland ◽  
Theresa Rogers ◽  
...  

Purpose To prospectively study the pharmacokinetics and toxicity profile of docetaxel in elderly patients with cancer. Patients and Methods Docetaxel was administered at a dose 75 mg/m2 once every 3 weeks to 25 elderly cancer patients aged ≥ 65 years and 26 cancer patients aged younger than 65 years. Pharmacokinetic studies and toxicity assessments were performed during the first cycle of therapy. Results Of 51 patients treated, 20 aged ≥ 65 years (median, 71 years; range, 65 to 80 years) and 20 aged younger than 65 years (median, 53 years; range, 26 to 64 years) were assessable for pharmacokinetic studies, and 39 were assessable for toxicity. Patient characteristics were similar (P ≥ .15) between the two cohorts. Mean docetaxel clearance was not altered in the elderly versus younger patients: 30.1 L/h (standard deviation [SD] 18.3 L/h) v 30.0 L/h (SD, 14.8 L/h; P = .98). The percentage of patients with grade 4 and febrile neutropenia was higher in the elderly (63% and 16%, respectively) versus younger (30% and 0%, respectively) cohort, although this observation did not reach a level of statistical significance (P = .056). From logistic regression analysis, the odds ratio for a patient aged 65 years was 1.98 for developing grade 4 neutropenia compared with a patient aged 50 years (P = .091). Conclusion Docetaxel plasma pharmacokinetics are unaltered in elderly patients. Patients aged ≥ 65 years appear to be more sensitive to docetaxel-induced neutropenia.


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