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Quinolones a Systematic Quest

Quinolones a Systematic Quest

Quinolones A Systematic Quest

David C. Hooper, M.D. Division of Infectious Diseases Control Unit Massachusetts© by General author Hospital Harvard Medical School ESCMID Online Lecture Library Timeline of Quinolone Development

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ESCMIDNorris S, Mandell Online GL in Andriole Lecture V (ed). The Library Quinolones 1988

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George Y. Lesher, Ph.D. ESCMID Online1926- Lecture1990 Library Surprise Beginnings O

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C2H5 © by author ESCMID Online Lecture Library Quinolones The First Decade (Childhood) • 1962 Discovery of Nalidixic Acid as anti- bacterial byproduct of chloroquine synthesis (Lesher) • 1964-66 Mechanisms of Action Defined (Goss, Dietz, Cook) » Inhibition of DNA synthesis » Conditional bactericidal activity • 1967 Nalidixic Acid released for clinical use for treatment of© urinary by author tract caused by enteric • 1969 Resistance to Nalidixic Acid in E. coli ESCMID mapped Online to chromosomal Lecture mutations Library (nalA,B) (Hane) Quinolones The Second Decade (Adolescence)

• 1970 Development of , the 1st pyrrolindinyl quinolone • 1975 Development of , the 1st piperazinyl quinolone • 1976 Discovery of DNA gyrase, the 1st type 2 (Gellert) • 1976 Development of , the 1st fluoroquinolone© andby tricyclicauthor quinolone • 1977 Nalidixic Acid resistance loci identified as encoding mutant subunits of DNA gyrase ESCMIDof E. coli Online (Gellert, LectureCozzarelli) Library

Piromidic Acid Pipemidic Acid

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ESCMID OnlineFlumequine Lecture Library Quinolones - The Third Decade (Adolescent Growth Spurt)

• 1986 released for clinical use in US (GU infections) • 1986 Development of , 1st 6, 8- difluoroquinolone (recognition of photosensitivity associated with 8-F) • 1987 released for clinical use in US (broad ©indications) by author • 1988-89 Identification of drug resistance by altered permeation for hydrophilic quinolones - active ESCMID efflux andOnline altered Lecture porins Library O O F COOH F COOH

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ESCMIDFleroxacin OnlineF Lecture Library Quinolone Phototoxicity

• UVA (320-420 nm) interactions • Generation of reactive oxygen species • Drug concentrations in skin • SARs – Position 8: C-halogen > N-H > C-H > C-O-R – Position 7: Alkylated© by authorrings increase t½

– Position 5: CH3 > H > NH2 ESCMID Online Lecture Library Quinolones - The Fourth Decade (Problems of Adolescence) • 1990 PO/IV released for clinical use in US (broad indications) • 1990 Discovery of Topoisomerase IV (Kato) • 1991 PO released in US (GU indications) • 1992 released and withdrawn due to unexpected rare but severe toxicities (Hemolytic©-Uremic by author Syndrome) • 1992 PO released in US, 1st once- daily fluoroquinolone • 1993ESCMID-94 Identification Online of Lecture quinolone Libraryinhibition of topoisomerase IV of E. coli O O F COOH F COOH

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C2H5 Enoxacin F C2H5 H3C O Lomefloxacin F COOH O F COOH HCl N N F © by author HN H3C N N N O * CH3 CH3

ESCMID Online LectureOfloxacin Library Temafloxacin F Quinolones - The Fourth Decade (Adulthood)

• 1994-96 Identification of topoisomerase IV as principal quinolone target in S. aureus and secondary target in E. coli • 1996 PO/IV and PO released in US (expanded Gram+ respiratory indications) • 1997 © by PO author (Respiratory/GU Indications) and PO/IV (broadest indications, 1st anti-anaerobic ESCMID quinolone) Online released Lecture in US Library O NH2 O F COOH F COOH H3C

H3C N N N HN N N O F CH3 H3C Sparfloxacin Levofloxacin O

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GrepafloxacinESCMID Online LectureTrovafloxacin Library F Quinolones - The Fourth Decade (Adults Have Their Ups & Downs) • 1998 Plasmid transferable quinolone resistance identified • 1999 Trovafloxacin use restricted due to rare but severe (? Legacy of temafloxacin) • 1999 Grepafloxacin withdrawn because of cardiac events. Sparfloxacin© by author also associated with arrhythmias • 1999 PO/IV and PO ESCMID released Online with a focus Lecture on respiratory Library tract indications Rare, Serious Idiosyncratic Reactions • Temafloxacin (1992) – Hemolytic uremic syndrome – Coagulopathy (35%) – Hepatic dysfunction (51%) – Reporting incidence ~1:6000 • Trovafloxacin (1999) – Symptomatic hepatitis© by author – Life-threatening in ~10% – Reporting incidence ~1:18,000 ESCMID OnlineBlum MD Lectureet al. 1994. ClinLibrary Infect Dis 18:946 Ball P et al. 1999. Drug Safety 21:407 Quinolones - The Fourth Decade (Adults Have Their Ups & Downs)

• 1999 Trovafloxacin use restricted due to rare but severe hepatotoxicity (? Legacy of temfloxacin) • 1999 Grepafloxacin withdrawn because of cardiac events. Sparfloxacin also associated with arrhythmias © by author • 1999 Gatifloxacin PO/IV and Moxifloxacin PO released with a focus on respiratory tract ESCMID indications Online Lecture Library Effects of Drugs on Cardiac Conduction a b Drug QTC Prolongation Ikr hERG IC30 (msec) (µM) (µM) Sparfloxacin 13-15 0.23 10 Grepafloxacin 10 27.2 39 Moxifloxacin 7 -- 92 Gatifloxacin 5-6 26.5 104 Terfenidine 46 © by author Erythromycin 8-15 aAnderson et al. 3rd ECC ClarithromycinESCMID Online2-6 bChen Lecture et al. ICAAC Library 2000 abstr 765 Quinolones - The Fourth Decade (Adults Have Their Ups & Downs)

• 1999 Trovafloxacin use restricted due to rare but severe hepatotoxicity (? Legacy of temfloxacin) • 1999 Grepafloxacin withdrawn because of cardiac events. Sparfloxacin also associated with arrhythmias © by author • 1999 Gatifloxacin PO/IV and Moxifloxacin PO released with a focus on respiratory tract ESCMID indications Online Lecture Library Quinolone Structure-Activity Relationships

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ESCMID Online Lecture Library Domagala JM. 1994. J Antimicrob Chemother 33:685 Quinolone Structure-Adverse Effects Relationships

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ESCMIDDomagala JM. Online 1994. J Antimicrob Lecture Chemother Library 33:685 Quinolones - The Fifth Decade (Adults Have Their Ups & Downs)

• 2002 Plasmid-encoded Qnr protein identified as protecting gyrase from quinolones • 2003 approved for community- acquired with 5-day regimen • 2006 Plasmid-encoded quinolone-modifying enzyme identified as mutant AAC(6’)-Ib • 2007 Plasmid-encoded© by QepAauthor efflux pump identified • 2008 Gatifloxacin withdrawn because of ESCMID dysglycemia Online events Lecture Library • 2009 First topoisomerase IV-DNA crystal structures with quinolone bound

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Laponogov I et al. Nature Struct Mol Biol. ESCMID Online Lecture2009; 16:667Library The Fluoroquinolone Family American Branch – The Sixth Decade 12 Approvals over 17 Years • Norfloxacin (Noroxin) • SparfloxacinXXX (Zagam) 1986 1996 • Ciprofloxacin (Cipro) • GrepafloxacinXXX (Raxar) 1987 PO, 1990 IV 1997 • Ofloxacin (Floxin) • TrovafloxacinXXX (Trovan) 1990 PO, 1992 IV 1997 • EnoxacinXXX (Penetrex) • GatifloxacinXXX (Tequin) 1991 © by author1999 • LomefloxacinXXX (Maxaquin) • Moxifloxacin (Avelox) 1992 1999 • LevofloxacinESCMID (Levaquin) Online Lecture• Gemifloxacin Library (Factive) 1996 2003 Adverse Effects of Fluoroquinolones • Gastrointestinal – , , • Central Nervous System – (trovafloxacin), insomnia, • Cardiovascular

– QTC prolongation (sparfloxacin, grepafloxacin > moxifloxacin) • Hepatic – Idiosyncratic hepatitis (trovafloxacin) • Metabolic – Dysglycemia (gatifloxacin > levofloxacin) • Skin © by author – Photosensitivity (sparfloxacin, lomefloxacin) – Other skin reactions (gemifloxacin) • Musculoskeletal – ESCMIDTendinopathy Online Lecture Library Quinolones – The Sixth Decade Senescence or New Generations to Follow The Search Goes On

• Keys to success: – Dealing with established resistance – Low potential for new resistance © by author – High tolerability (no surprises – better preclinical screening tools) ESCMID Online Lecture Library Problems With Development of Bacterial Resistance to Fluoroquinolones

Staphylococci (MRSA, MRSE) 60-95%

Pseudomonas aeruginosa 5-30% Campylobacter jejuni 3-50% 8-26% Neisseria gonorrheae© by author 6-70% 3% ESCMID Online Lecture Library Predicting Resistance Potential: (Which Quinolone Will Live the Longest?) • Determinants of bacterial resistance

– Activity against both target enzymes, DNA gyrase and DNA topoisomerase IV – Effects of native bacterial efflux systems – Potency that keeps© by drug author concentrations above the MIC of first-step resistant mutants (mutant prevention ESCMIDconcentration) Online Lecture Library O F CO2H

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H2N Activity: S. pneumoniae (16x) Other streptococci (16-32x) (Relative to Enterococci (16x) Ciprofloxacin) S. aureus (>2-32x) B. fragilis (64x) P. aeruginosa (1-6x) © by author→ µ : 500mg PO Cmax 4.6 g/ml t 1/2 = 4.5-5h; renal (70%)

Vd = 1.8 liters ESCMID OnlineAnderson Lecture DL. Drugs Library of Today 2008; 44:489. /Ulifloxacin

Activity: S. pneumoniae (1x) S. pyogenes (1x) (Relative to Enterococci (1x) Levofloxacin) S. aureus (1x) Klebsiella spp. (4x) © byEnterobacter author spp. (4x) P. aeruginosa (0.5-2x)

ESCMIDMontanari MP Online et al. Antimicrob Lecture Agents Chemother. Library 2001; 45:3616

Organism MIC (median, μg/ml) pH 5.0 pH 7.3 Fin Cip Fin Cip E. coli CipS 0.031 0.5 0.125 0.016 CipNS 8 ≥16 ≥32 ≥16 K. pneumoniae CipS 0.063 1.0 0.125 0.031 CipNS 2 © by ≥16 author 6.0 3.0 S. aureus CipS 0.125 2.0 0.25 0.5 CipNS 8.0 ≥16 8.0 ≥16 ESCMID Online Lecture Library 48th ICAAC, IDSA Abstract F1-2037

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HN Activity: S. aureus (2-4x) S. pneumoniaea (16x) (Relative to Enterococci (4-16x) Moxifloxacin) K. pneumoniae (1x) E. cloacae (0.5x) © byP. authoraeruginosa (~1x) [aAdvantage maintained vs parC gyrA double mutants of S. pneumoniae Serial passage selection: 4-16 x ↑ MIC to max of 2 μg/ml] Park H-S et al. Antimicrob Agents Chemother. 2006; 50:2261 KosowskaESCMID-Shick KOnline et al. Antimicrob Lecture Agents Chemother. Library 2006; 50:2064 (RX-3341, ABT492)

S. aureus MRSA >64x S. aureus MSSA >64x Enterococci 16x S. pyogenes >64x S.epidermidis 32x Activity: S. pneumoniae 128x H. influenzae 16-32x (Relative to L. pneumophila 8x Levofloxacin) © byChlamydia author spp. 2-32x K. pneumoniae 4x M. pneumoniae 2x ESCMID Online LectureP. aeruginosa Library 0.5-1x WCK-771 (S-)

Activity: S. pneumoniae (≥2x) S. pyogenes (2x) (Relative to S. aureusa (16-32x) Levofloxacin) S. epidermidis (16-32x)

Pharmacokinetics:© by600mg author IV → Cmax 4.0 µg/ml t 1/2 = 6 h [aFirst-step selection: S. aureus mutations in gyrA with 2x ↑ MIC] Jacobs MR et al. Antimicrob Agents Chemother 2004; 48:3338 ESCMID AlOnline-Laham A et al.Lecture J Antimicrob ChemotherLibrary 2005; 56:1130 Bhagwat SS et al. Antimicrob Agents Chemother. 2006; 50:3568 DX-619 OO

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H2N OMe F Activity: S. pneumoniae (≥128x) Other streptococci (32-64x) (Relative to Enterococci (64x) Levofloxacin) S. aureusa (16-128x) Klebsiella spp. (1x) © byP. aeruginosaauthor (2x) Pharmacokinetics: :serum ratio 5.3 (3x > cipro) in mice Fujikawa K et al. Antimicrob Agents Chemother. 2005; 49:3040 ESCMIDWickman PAOnline et al. Antimicrob Lecture Agents Chemother.Library 2006; 50:2255 Fukuda Y et al. Antimicrob Agents Chemother. 2006; 50:121 DC-159a

Activity: S. pneumoniae (8-32x) Enterococci (8x) (Relative to S. aureus (4-16x) Levofloxacin) H. influenzae (1x) Peptostreptococcus (32x) © byB. fragilisauthor (16x) K. pneumoniae (1x) P. aeruginosa (0.5x) ESCMIDHoshino K et Onlineal. Antimicrob Lecture Agents Chemother. Library 2008; 52:65 PD 0305970 and PD 0326448

Activity: S. aureus (2-32x) S. pneumoniaea (16-32x) (Relative to Enterococci (128x) Levofloxacin) S. pyogenes (64x) K. pneumoniae (0.12x) © byE. author cloacae (0.25x) [aFirst-step mutants in gyrB (2x ↑ MIC) or gyrB parE (4x ↑ MIC)] Efficacy > levofloxacin in murine pneumococcal pneumonia model ESCMIDHuband MD Onlineet al. Antimicrob Lecture Agents Chemother. Library 2007; 51:1191 ACH-702

a Activity: S. aureus (>32->64x) S. pneumoniae (16x) (Relative to Enterococci (>8->32x) Levofloxacin) S. pyogenes (16x) K. pneumoniae (2x) © byEnterobacter author spp. (0.25-1x) P. aeruginosa (0.5x)

[MIC90: B. fragilis 0.25 μg/ml, Peptostreptococcus 0.06 μg/ml] [aSingle-step gyrA mutants with 4x ↑ MIC] ESCMID Online48th ICAAC, Lecture IDSA Abstract Library F1-2021, F1-2022 Long Life Sometimes Needs Help from the Doctor(s)

• Monitoring resistance

• Good Infection Control to Limit Spread • Focused Use to Limit Selective Pressures • Adequate Dosing to Limit Mutant Selection • Possible Use of Combination© by author Regimens: – With Other – Specific Inhibitors of Resistance Mechanisms ESCMID Online Lecture Library