Adverse Cutaneous Reactions to Targeted Anti Cancer...
Transcript of Adverse Cutaneous Reactions to Targeted Anti Cancer...
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Adverse Cutaneous Reactions to Targeted Anti‐Cancer Therapies
Jonathan Cotliar, MDClinical Associate Professor & Chief
Division of DermatologyCity of Hope National Medical Center
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DisclosuresDisclosures
• Consultant for Xcovery
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ObjectivesObjectives
• Discuss the role of the dermatologist in the care of cancer patientsp
• Recognize the diverse clinical presentation of adverseRecognize the diverse clinical presentation of adverse cutaneous reactions to traditional chemotherapeutic agents
• Recognize and treat cutaneous toxicities to targeted anti‐cancer drugs
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What is Oncodermatology?What is Oncodermatology?
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OncodermatologyOncodermatology• Expanding dermatology
b i ltsubspecialty
• Partnership with oncologists
• Availability Afatinib (Gilotrif)
EGFR Inhibitors• Supportive care to facilitate cancer treatment
F ili i i h f
EGFR Inhibitors
• Familiarity with spectrum of chemotherapeutics & targeted anti‐cancer drugs and their associated cutaneous toxicities
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Challenges in OncodermatologyChallenges in Oncodermatology
• Keeping patients on therapy
• Toxicities worse than cancer
• Inability to improve cutaneous toxicities
• Lack of dermatologists/ access
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ChemotherapeuticsChemotherapeutics
• Alkylating agentsClassic: cyclophosphamide, ifosmamide, thiotepaPlatinum agents: cisplatin, carboplatin, oxaliplatin • Mitotic inhibitors
Taxanes: docetaxel, paclitaxel
• AntimetabolitesAnalogs: cytarabine, fludarabine, cladribine, gemcitabine,
pemetrexedFluorouracil: 5FU, capecitabine, tegafur
Vinca alkaloids: vincristine, vinblastine, vinorelbineMacrocyclic analogue: eribulin
• Topoisomerase inhibitorsFluorouracil: 5FU, capecitabine, tegafur
• Antitumor antibioticsAnthracyclines: doxorubicin, daunorubicin
• Topoisomerase inhibitorsTopoisomerase I: topotecan, irinotecanTopoisomerase II: etoposide, teniposide, amsacrine
Bleomycin
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Targeted anti‐cancer agentsTargeted anti cancer agentsMonoclonal Antibodies• Rituximab• Trastuzumab
Immunomodulatory Drugs• Thalidomide• Lenalidomide• Trastuzumab
• Alemtuzumab• Cetuximab• Bevacizumab• Panitumumab• Ofatumumab• Pertuzumab• Obinutuzumab
• Lenalidomide• Ipilimumab• Pomalidomide• Binatumomab• Pembrolizumab• Nivolumab
Signal Transduction InhibitorsObinutuzumab• Ramucirumab• Siltuximab• Dinutuximab• Darzalex/daratumumab• Elotuzumab• Ibritumomab tiuxetan• Tositumumab
Signal Transduction Inhibitors• Imatinib regorafinib• Gefitinib cabozantinib• Trametinib ponatinib• Erlotinib dabrafenib• Sorafenib afatinib• Dasatinib ibrutinib• Sunitinib ceritinibTositumumab
• Brentuximab• Ado‐trastuzumab
Transcription/ Translational Inhibitors• Decitabine• Vorinostat• Romidepsin
Sunitinib ceritinib• Lapatinib zydelig• Temsirolimus levatinib• Nilotinib palbociclib• Everolimus alectinib• Pazopanib bosutinib• Vandetanib Ziv‐affibercept• Vemurafenib Vismodegibp
• Omacetaxine• Belinostat• Panobinostat• Trabectedin
DNA Repair Inhibitors• Olaparib
g• Crizotinib Axitinib• Ruxolitinib
Proteosome Inhibitors• Bortezomib• Carfilzomab• Ixazomib
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Toxic Erythema of Chemotherapy (TEC)Toxic Erythema of Chemotherapy (TEC)
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Toxic Erythema of Chemotherapy (TEC)B l i l JAAD 2008Bolognia et al. JAAD 2008
•• Overlap of reactions to chemotherapy Overlap of reactions to chemotherapy
•• Toxic effect on eccrine ducts, acrosyringium, epidermisToxic effect on eccrine ducts, acrosyringium, epidermis
•• Areas of involvement reflect high density of eccrine glandsAreas of involvement reflect high density of eccrine glandsAreas of involvement reflect high density of eccrine glandsAreas of involvement reflect high density of eccrine glands
•• Shared histologic featuresShared histologic features
•• CytarabineCytarabine, Cyclophosphamide, Anthracyclines, 5, Cyclophosphamide, Anthracyclines, 5‐‐FU, FU, Capecitabine, Taxanes, MethotrexateCapecitabine, Taxanes, Methotrexate
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Toxic Erythema of Chemotherapy (TEC)
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TECTEC
• Hands, feet,• Flexural, intertriginous• Painful or asymptomatic• Desquamation• Recurrent/ progressive
Hi t l i f t• Histologic features:– Keratinocyte dysmaturation,
apoptosis, necrosisl d i– Vacuolar degeneration
– Eccrine squamous syringometaplasia
Parker TL, Cooper DL, Seropian SE, Bolognia JL. Toxic erythema of chemotherapy followingi.v. BU plus fludarabine for allogeneic PBSC transplant. Bone marrow transplantation. 2012.
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Toxic Erythema of ChemotherapyB l i l 2008Bolognia et al. 2008
•• AraC earsAraC ears • Acral erythema•• Burgdorf’s reactionBurgdorf’s reaction
•• Eccrine squamous syringometaplasiaEccrine squamous syringometaplasia
Acral erythema
–– Acral erythrodysesthesiaAcral erythrodysesthesiaChemotherapyChemotherapy induced acralinduced acral•• Intertriginous eruption associated Intertriginous eruption associated
with chemotherapywith chemotherapy
•• Flexural erythematous eruptionFlexural erythematous eruption
–– ChemotherapyChemotherapy‐‐induced acral induced acral erythemaerythema
–– HandHand‐‐foot syndromefoot syndromePalmarPalmar plantar erythemaplantar erythema
•• Intertrigo dermatitisIntertrigo dermatitis
•• Neutrophilic eccrine hidradenitisNeutrophilic eccrine hidradenitis
h hh h hh
–– PalmarPalmar‐‐plantar erythemaplantar erythema–– PalmarPalmar‐‐plantar erythrodysesthesiaplantar erythrodysesthesia–– Toxic acral erythemaToxic acral erythema–– Toxic erythema of the palms andToxic erythema of the palms and•• ChemotherapyChemotherapy‐‐induced hidradenitisinduced hidradenitis
•• Epidermal dysmaturationEpidermal dysmaturation
•• ChemotherapyChemotherapy‐‐induced epidermalinduced epidermal
–– Toxic erythema of the palms and Toxic erythema of the palms and solessoles
ChemotherapyChemotherapy induced epidermal induced epidermal dystrophydystrophy
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TEC PearlsTEC Pearls
• Tender rather than pruritic
• Can develop late and last 2‐3 weeks beyond tx
• Mistaken for acute GVHD
• Sometimes anatomic site trumps morphology
• Check dressingsg
• Pyridoxine (Vitamin B6)?
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Pyridoxine (B6) for TEC?Pyridoxine (B6) for TEC?
• Ota et al. 2014‐ 60mg QD ineffective for HFS in CRC pts on capecitabine
• Braik et al 2014‐ 100mg QD ineffective for HFSBraik et al. 2014 100mg QD ineffective for HFS
• Myung et al. 2015‐ effective for tx HFS but not prophylaxis
• Chen et al. 2013‐ 400mg pyridoxine may be effective to prevent HFS
• Macedo et al. 2014‐ celecoxib efficacious for prophylaxis of HFS
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Hand Foot Syndrome
• Subtype of TEC
• Prodrome of dysesthesia
• Painful, symmetric erythema, edema
• Blisters, erosions
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Hand Foot SyndromeHand Foot Syndrome
Acral erythrodysesthesiaAcral erythrodysesthesiaChemotherapyChemotherapy‐‐induced acral erythemainduced acral erythemaAcral erythemaAcral erythemaP lP l l t thl t thPalmarPalmar‐‐plantar erythemaplantar erythemaPalmarPalmar‐‐plantar erythrodysesthesiaplantar erythrodysesthesiaToxic acral erythemaToxic acral erythemaToxic acral erythemaToxic acral erythemaToxic erythema of the palms and solesToxic erythema of the palms and soles
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Toxic Erythema of Chemotherapy:Hand Foot Syndrome subtypeHand Foot Syndrome subtype
(HFS)
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How to grade HFSHow to grade HFS
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Nail ToxicitiesNail Toxicities
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Nail ToxicitiesNail Toxicities
• Taxanes, Anthracyclines, Capecitabine
• Docetaxel 35%• Paclitaxel 44%
Capriotti K, Capriotti JA, Lessin S, et al. The risk of nail changes with taxane chemotherapy: a systematic review of the literatureand meta‐analysis. The British journal of dermatology. Feb 21 2015.
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Nail ToxicitiesNail Toxicities
• Treatment strategies:Treatment strategies:
‐ Minimizing wet work, hand work‐ Refraining from
manicures/pedicures‐ Vinegar soaksVinegar soaks‐ Cold gloves?‐ Culture!!!
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Secondary Nail InfectionsSecondary Nail Infections
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Prevention/ Treatment of nail infectionsPrevention/ Treatment of nail infections
• Suspect gram negative, fungal organisms• Culture!!!• Ciprofloxacin• Examine prior to treatment• Avoid manicures/pedicures• Mupirocin, Cephalexin for Gram+
Vi k QD BID• Vinegar soaks QD‐BID (1/2 cup warm H2O, 1/2 cup white vinegar)
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Toxicities to targeted anti‐cancer agentsToxicities to targeted anti cancer agents
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Hand Foot Skin Reaction(HFSR)
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Zuo et al. JAMA Derm Feb 2015
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Multikinase inhibitors (MKIs) that cause HFSRMultikinase inhibitors (MKIs) that cause HFSR
• Sorafenib‐ VEGFR, PDGFR, C‐raf, B‐raf‐ Renal Cell Ca, Hepatocellular CaHFSR 34%
• Sunitinib‐ VEGFR, PDGFR, c‐KIT, FLT3, RET, G‐CSF1R‐ Renal Cell Ca, GISTHFSR 19%
• Pazopanib‐ VEGFR‐1, VEGFR‐2, VEGFR‐3, PDGFR, c‐KIT‐ Renal Cell Ca, soft tissue sarcomaHFSR 4.5%
• Regorafenib‐ VEGFR,TIE‐2, KIT, REF, RAF‐1, BRAF, PDGFR – Colorectal Ca, Hepatocellular Ca, GISTHFSR 61%
• Axitinib‐ VEGFR‐1, VEGFR‐2, VEGFR‐3‐ Renal Cell CaHFSR 29%
Cabozantinib‐VEGFR‐2, c‐MET, RET‐Medullary Thyroid CaHFSR 54%HFSR 54%
Vemurafenib, Dabrafenib‐BRAF‐melanomaHFSR 10‐20%
Lapatinib‐ dual TKI (HER2/neu, EGFR)‐ Metastatic Breast ca
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SunitinibSunitinib
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SorafenibSorafenib
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CabozantinibCabozantinib
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RegorafenibRegorafenib
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AxitinibAxitinib
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SorafenibSorafenib
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What’s the difference?What s the difference?
Hand Foot Syndrome Hand Foot Skin ReactionHand Foot Syndrome Hand Foot Skin Reaction
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What’s the difference?
HFSR HFS HFSR
What s the difference?
HFSR HFS HFSR
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What’s the difference?What s the difference?
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How to treat HFS/HFSRHow to treat HFS/HFSR• Minimizing hand/foot use
O th ti tt k id ti ht• Orthotics, cotton socks, avoid tight‐fitting shoes, running
• Emollients• Keratolytics‐ urea• High‐potency topical steroids• Topical anesthetics• NSAIDs, GABA agonists, opioids• Pyridoxine (B6)Pyridoxine (B6)• Cold gloves• Celecoxib• Vit E
• Stop anti‐cancer drug/ dose reduction
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Targeted agents for melanomaTargeted agents for melanoma
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BRAF InhibitorsBRAF Inhibitors
• Metastatic or unresectable melanomamelanoma
• Vemurafenib, Dabrafenib
• Fatigue, arthralgias, nausea, g , g , ,diarrhea, AKI
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BRAF InhibitorsBRAF Inhibitors• 74% develop skin toxicity• Rash in nearly 18‐27% (dose‐dependent)Rash in nearly 18 27% (dose dependent)• Erythema, morbilliform, papulopustular, KP‐like
• Verruca• Eruptive KA, SCC‐ 20%• Warty dyskeratoma• Grover’s disease• Wild‐type melanoma• Nevi
H d f t ki ti• Hand‐foot‐skin reaction• Photosensitivity‐ 42%• Keratosis pilaris‐like• Pruritus• Acneiform eruptionAcneiform eruption• Alopecia• Panniculitis
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VemurafenibVemurafenib
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VemurafenibVemurafenib
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Belum VR, Fischer A, Choi JN, Lacouture ME. Dermatological adverse events from BRAFDermatological adverse events from BRAF inhibitors: a growing problem. Current oncologyreports. Jun 2013;15(3):249‐259.
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Lacouture ME, Duvic M, Hauschild A, etal. Analysis of dermatologic events in vemurafenib‐treated patients with melanoma. The oncologist. 2013;18(3):314‐322.
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MEK InhibitorsMEK Inhibitors
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MEK InhibitorsMEK Inhibitors• Trametinib‐ inhibits MEK1/MEK2‐
alone or w/ dabrafenibalone or w/ dabrafenib• Cobimetinib (w/ vemurafenib)• Selumetinib, Binimetinib
• Morbilliform eruption (dose‐dependent) 46‐74%
• Papulopustular eruption‐ decreased incidence in BRAF/MEK combo
• Xerosis• Alopecia• Paronychia• Mitigate eruptive SCC from BRAF
inhibitors
Jae Jung, MD, PhD
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Checkpoint InhibitorsCheckpoint Inhibitors
http://www.nzmu.co.nz/anti‐pd‐1‐inhibitors
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IpilimumabIpilimumab• Fully human monoclonal antibody
to cytotoxic T‐lymphocyte antigen (CTLA)‐4
• Approved for unresectable or metastatic melanoma
• Most common toxicities:RashPruritusDiarrhea/ colitis http://www.nzmu.co.nz/anti‐ctla‐4‐inhibitors
earliest onset
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IpilimumabIpilimumab• Incidence of Derm AEs 44% • High‐grade 2.4%
• Pruritus
• Morbilliform, reticulated, erythematous, papular, sarcoidal
• Vitiligo (favorable prognosis)
• Perivascular lymphocytes, i hileosinophils
• Reactive treatment with topical/ systemic steroids antihistaminessystemic steroids, antihistamines
Lacouture ME, Wolchok JD, Yosipovitch G, Kahler KC, Busam KJ, Hauschild A. Ipilimumab in patients with cancer and the management of dermatologic adverse events. Journal of the American Academy of Dermatology. Jul 2014;71(1):161‐169.
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IpilimumabIpilimumab
M billif P lMorbilliform Papular
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Lacouture ME, Wolchok JD, Yosipovitch G, Kahler KC, Busam KJ, Hauschild A.Ipilimumab in patients with cancer and the management of dermatologicand the management of dermatologic adverse events. Journal of the AmericanAcademy of Dermatology. Jul 2014;71(1):161‐169.
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PD‐1, PD‐L1 InhibitorsPD 1, PD L1 Inhibitors
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PD‐1 InhibitorsPD 1 Inhibitors• Nivolumab‐melanoma, NSCLC, RCC, HL• Pembroli mab melanoma NSCLC• Pembrolizumab‐melanoma, NSCLC,
H&N SCC
• FatigueP i hill i f i ti• Pyrexia, chills, infusion reactions
• Diarrhea/ colitis• Hypophysitis• Hypo/hyperthyroidism• Adrenal insufficiency• Hepatitis• Pneumonitis• Myasthenia gravisy g• Uveitis• Interstitial nephritis• Pancreatitis
Naidoo J, Page DB, Li BT, et al. Toxicities of the anti‐PD‐1 and anti‐PD‐L1 immune checkpoint antibodies. Annals of oncology : official journal of the European Society for Medical Oncology / ESMO. Dec 2015;26(12):2375‐2391.
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PD‐1 Inhibitors and Skin ToxicityPD 1 Inhibitors and Skin Toxicity
42% P b li b t / ki AE 42% Pembrolizumab pts w/ skin AEsMorbilliformPapulopustularPruritusHypopigmentationAlopecia
Lipson EJ Forde PM Hammers HJ Emens LA Taube JM Topalian SL Antagonists ofLipson EJ, Forde PM, Hammers HJ, Emens LA, Taube JM, Topalian SL. Antagonists of PD‐1 and PD‐L1 in Cancer Treatment. Seminars in oncology. Aug 2015;42(4):587‐600.
Sanlorenzo M, Vujic I, Daud A, et al. Pembrolizumab CutaneousAdverse Events and Their Association With Disease Progression.JAMA dermatology. Jul 29 2015.
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JAAD March 2016
82 patients
40/82 (49%) developed adverse skin events
Unclear if adverse events surrogate markersof efficacy
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PD‐1 Inhibitors and PsoriasisPD 1 Inhibitors and Psoriasis
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PD‐1 Inhibitors and PsoriasisPD 1 Inhibitors and Psoriasis
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PD‐1 Inhibitors and PsoriasisPD 1 Inhibitors and Psoriasis
Pembrolizumab
Nivolumab
Sahuquillo‐Torralba A, Ballester‐Sanchez R, Pujol‐Marco C, Botella‐Estrada R. Pembrolizumab: a new Drug That Can Induce Exacerbations of Psoriasis.Actas dermo‐sifiliograficas. Nov 3 2015.
Ohtsuka M, Miura T, Mori T, Ishikawa M, Yamamoto T. Occurrence of Psoriasiform Eruption During Nivolumab Therapy for Primary Oral Mucosal Melanoma. JAMA dermatology. Jul 2015;151(7):797‐799.
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Pembrolizumab and Hypertrophic Lichen Planus
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Pembrolizumab and SarcoidosisPembrolizumab and Sarcoidosis
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Hedgehog pathway InhibitorsHedgehog pathway Inhibitors
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Hedgehog pathway InhibitorsHedgehog pathway Inhibitors• Vismodegib, Sonidegib
M i BCC l ll d d• Metastatic BCC or locally advanced that can’t be tx with surgery/XRT
• 25% serious adverse events• Leg cramps/muscle spasms (68%)‐
amlodipine, Gatorade, Mg• Alopecia (10‐63%)‐minoxidil• Dysgeusia (23 57%) zinc• Dysgeusia (23‐57%)‐ zinc,
Synsepalum dulcificum (“miracle fruit”)
F ti• Fatigue• Nausea• Diarrhea• KA/SCC?KA/SCC?
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VismodegibVismodegib
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ConclusionsConclusions
•• Oncodermatology will continue to growOncodermatology will continue to grow
•• Universal nomenclature is importantUniversal nomenclature is important
•• Dermatology participation in pilot studies, grading Dermatology participation in pilot studies, grading schema management of cancer pts is vitalschema management of cancer pts is vitalschema, management of cancer pts is vitalschema, management of cancer pts is vital
•• Be aware of autoimmune dermatoses from PDBe aware of autoimmune dermatoses from PD‐‐11Be aware of autoimmune dermatoses from PDBe aware of autoimmune dermatoses from PD 1 1 inhibitorsinhibitors
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Dermatology at City of HopeDermatology at City of Hope
• Oncodermatology clinic• Primary care dermatology• Inpatient consult service
• Multidisciplinary GVHD clinic• Multidisciplinary CutaneousMultidisciplinary Cutaneous
lymphoma clinic• Cutaneous Immunotherapy
clinicclinic• Dermatopathology• Oncodermatology fellowship