Measuring Toxic Effects and Time to Treatment Failure for Nivolumab Plus Ipilimumab in Melanoma

Nivolumab plus ipilimumab (nivo + ipi) is a standard treatment of advanced melanoma. Two randomized trials describe high objective response rates by Response Evaluation Criteria in Solid Tumors. The trials assessed toxic effects using the Common Terminology Criteria for Adverse Events (CTCAE), which...

Full description

Saved in:
Bibliographic Details
Published in:JAMA oncology Vol. 4; no. 1; p. 98
Main Authors: Shoushtari, Alexander N, Friedman, Claire F, Navid-Azarbaijani, Pedram, Postow, Michael A, Callahan, Margaret K, Momtaz, Parisa, Panageas, Katherine S, Wolchok, Jedd D, Chapman, Paul B
Format: Journal Article
Language:English
Published: United States 01.01.2018
Subjects:
ISSN:2374-2445, 2374-2445
Online Access:Get more information
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract Nivolumab plus ipilimumab (nivo + ipi) is a standard treatment of advanced melanoma. Two randomized trials describe high objective response rates by Response Evaluation Criteria in Solid Tumors. The trials assessed toxic effects using the Common Terminology Criteria for Adverse Events (CTCAE), which may underestimate incidence of clinically significant immune-related adverse events (AEs). To describe detailed toxic effects and time to treatment failure of patients with melanoma treated with nivo + ipi in a prospective cohort. A cohort of 64 adults with advanced or unresectable melanoma were examined at a single tertiary cancer and enrolled in an expanded access program of nivo + ipi conducted from December 2014 to January 2016. Intravenous nivolumab (1 mg/kg) and ipilimumab (3 mg/kg) administered every 3 weeks for up to 4 doses, followed by nivolumab (3 mg/kg) every 2 weeks or pembrolizumab (2 mg/kg) every 3 weeks until unacceptable toxic effects, disease progression, or complete response. Clinically significant immune-related AEs were defined as CTCAE grade 2 or higher or any immune-related AEs requiring systemic steroids. Time to treatment failure was defined as the interval between initiating therapy and the earliest of clinical progression, new locally directed or systemic treatment other than anti-programmed cell death 1 protein (anti-PD-1) monotherapy, or death. Overall 64 adults with advanced or unresectable melanoma were enrolled (male to female ratio, 1:1; median [range] age, 56 [22-82] years); 25 patients (39%) received all 4 doses of nivo + ipi, and 31 patients (48%) received no maintenance anti-PD-1 therapy. Most who discontinued treatment (n = 31 [80%]) stopped because of toxic effects. Among those patients who were progression free at 12 weeks, time to treatment failure was similar between those who did or did not modify therapy for toxic effects. Fifty-eight patients (91%) had a clinically significant immune-related AE (median, 2/patient), and 46 patients (72%) required systemic steroids. Infliximab or mycophenolate was required in 16 patients (25%) for steroid-refractory immune-related AEs. Seven patients (11%) developed hyperglycemia, 32 patients (50%) had an emergency department visit, and 23 patients (36%) required a hospital admission related to an immune-related AE. Four of 31 patients (13%) who stopped combination therapy early for toxic effects developed a new, clinically significant immune-related AE more than 16 weeks after the last treatment. We observed a 91% incidence of clinically significant immune-related AEs leading to frequent emergency department visits, hospitalizations, and systemic immunosuppression. Immuno-oncology trials should routinely report these metrics. Most patients do not tolerate 4 doses of nivo + ipi; however, 4 doses may not be required for clinical benefit.
AbstractList Nivolumab plus ipilimumab (nivo + ipi) is a standard treatment of advanced melanoma. Two randomized trials describe high objective response rates by Response Evaluation Criteria in Solid Tumors. The trials assessed toxic effects using the Common Terminology Criteria for Adverse Events (CTCAE), which may underestimate incidence of clinically significant immune-related adverse events (AEs). To describe detailed toxic effects and time to treatment failure of patients with melanoma treated with nivo + ipi in a prospective cohort. A cohort of 64 adults with advanced or unresectable melanoma were examined at a single tertiary cancer and enrolled in an expanded access program of nivo + ipi conducted from December 2014 to January 2016. Intravenous nivolumab (1 mg/kg) and ipilimumab (3 mg/kg) administered every 3 weeks for up to 4 doses, followed by nivolumab (3 mg/kg) every 2 weeks or pembrolizumab (2 mg/kg) every 3 weeks until unacceptable toxic effects, disease progression, or complete response. Clinically significant immune-related AEs were defined as CTCAE grade 2 or higher or any immune-related AEs requiring systemic steroids. Time to treatment failure was defined as the interval between initiating therapy and the earliest of clinical progression, new locally directed or systemic treatment other than anti-programmed cell death 1 protein (anti-PD-1) monotherapy, or death. Overall 64 adults with advanced or unresectable melanoma were enrolled (male to female ratio, 1:1; median [range] age, 56 [22-82] years); 25 patients (39%) received all 4 doses of nivo + ipi, and 31 patients (48%) received no maintenance anti-PD-1 therapy. Most who discontinued treatment (n = 31 [80%]) stopped because of toxic effects. Among those patients who were progression free at 12 weeks, time to treatment failure was similar between those who did or did not modify therapy for toxic effects. Fifty-eight patients (91%) had a clinically significant immune-related AE (median, 2/patient), and 46 patients (72%) required systemic steroids. Infliximab or mycophenolate was required in 16 patients (25%) for steroid-refractory immune-related AEs. Seven patients (11%) developed hyperglycemia, 32 patients (50%) had an emergency department visit, and 23 patients (36%) required a hospital admission related to an immune-related AE. Four of 31 patients (13%) who stopped combination therapy early for toxic effects developed a new, clinically significant immune-related AE more than 16 weeks after the last treatment. We observed a 91% incidence of clinically significant immune-related AEs leading to frequent emergency department visits, hospitalizations, and systemic immunosuppression. Immuno-oncology trials should routinely report these metrics. Most patients do not tolerate 4 doses of nivo + ipi; however, 4 doses may not be required for clinical benefit.
Nivolumab plus ipilimumab (nivo + ipi) is a standard treatment of advanced melanoma. Two randomized trials describe high objective response rates by Response Evaluation Criteria in Solid Tumors. The trials assessed toxic effects using the Common Terminology Criteria for Adverse Events (CTCAE), which may underestimate incidence of clinically significant immune-related adverse events (AEs).IMPORTANCENivolumab plus ipilimumab (nivo + ipi) is a standard treatment of advanced melanoma. Two randomized trials describe high objective response rates by Response Evaluation Criteria in Solid Tumors. The trials assessed toxic effects using the Common Terminology Criteria for Adverse Events (CTCAE), which may underestimate incidence of clinically significant immune-related adverse events (AEs).To describe detailed toxic effects and time to treatment failure of patients with melanoma treated with nivo + ipi in a prospective cohort.OBJECTIVETo describe detailed toxic effects and time to treatment failure of patients with melanoma treated with nivo + ipi in a prospective cohort.A cohort of 64 adults with advanced or unresectable melanoma were examined at a single tertiary cancer and enrolled in an expanded access program of nivo + ipi conducted from December 2014 to January 2016.DESIGN, SETTING, AND PARTICIPANTSA cohort of 64 adults with advanced or unresectable melanoma were examined at a single tertiary cancer and enrolled in an expanded access program of nivo + ipi conducted from December 2014 to January 2016.Intravenous nivolumab (1 mg/kg) and ipilimumab (3 mg/kg) administered every 3 weeks for up to 4 doses, followed by nivolumab (3 mg/kg) every 2 weeks or pembrolizumab (2 mg/kg) every 3 weeks until unacceptable toxic effects, disease progression, or complete response.INTERVENTIONSIntravenous nivolumab (1 mg/kg) and ipilimumab (3 mg/kg) administered every 3 weeks for up to 4 doses, followed by nivolumab (3 mg/kg) every 2 weeks or pembrolizumab (2 mg/kg) every 3 weeks until unacceptable toxic effects, disease progression, or complete response.Clinically significant immune-related AEs were defined as CTCAE grade 2 or higher or any immune-related AEs requiring systemic steroids. Time to treatment failure was defined as the interval between initiating therapy and the earliest of clinical progression, new locally directed or systemic treatment other than anti-programmed cell death 1 protein (anti-PD-1) monotherapy, or death.MAIN OUTCOMES AND MEASURESClinically significant immune-related AEs were defined as CTCAE grade 2 or higher or any immune-related AEs requiring systemic steroids. Time to treatment failure was defined as the interval between initiating therapy and the earliest of clinical progression, new locally directed or systemic treatment other than anti-programmed cell death 1 protein (anti-PD-1) monotherapy, or death.Overall 64 adults with advanced or unresectable melanoma were enrolled (male to female ratio, 1:1; median [range] age, 56 [22-82] years); 25 patients (39%) received all 4 doses of nivo + ipi, and 31 patients (48%) received no maintenance anti-PD-1 therapy. Most who discontinued treatment (n = 31 [80%]) stopped because of toxic effects. Among those patients who were progression free at 12 weeks, time to treatment failure was similar between those who did or did not modify therapy for toxic effects. Fifty-eight patients (91%) had a clinically significant immune-related AE (median, 2/patient), and 46 patients (72%) required systemic steroids. Infliximab or mycophenolate was required in 16 patients (25%) for steroid-refractory immune-related AEs. Seven patients (11%) developed hyperglycemia, 32 patients (50%) had an emergency department visit, and 23 patients (36%) required a hospital admission related to an immune-related AE. Four of 31 patients (13%) who stopped combination therapy early for toxic effects developed a new, clinically significant immune-related AE more than 16 weeks after the last treatment.RESULTSOverall 64 adults with advanced or unresectable melanoma were enrolled (male to female ratio, 1:1; median [range] age, 56 [22-82] years); 25 patients (39%) received all 4 doses of nivo + ipi, and 31 patients (48%) received no maintenance anti-PD-1 therapy. Most who discontinued treatment (n = 31 [80%]) stopped because of toxic effects. Among those patients who were progression free at 12 weeks, time to treatment failure was similar between those who did or did not modify therapy for toxic effects. Fifty-eight patients (91%) had a clinically significant immune-related AE (median, 2/patient), and 46 patients (72%) required systemic steroids. Infliximab or mycophenolate was required in 16 patients (25%) for steroid-refractory immune-related AEs. Seven patients (11%) developed hyperglycemia, 32 patients (50%) had an emergency department visit, and 23 patients (36%) required a hospital admission related to an immune-related AE. Four of 31 patients (13%) who stopped combination therapy early for toxic effects developed a new, clinically significant immune-related AE more than 16 weeks after the last treatment.We observed a 91% incidence of clinically significant immune-related AEs leading to frequent emergency department visits, hospitalizations, and systemic immunosuppression. Immuno-oncology trials should routinely report these metrics. Most patients do not tolerate 4 doses of nivo + ipi; however, 4 doses may not be required for clinical benefit.CONCLUSIONS AND RELEVANCEWe observed a 91% incidence of clinically significant immune-related AEs leading to frequent emergency department visits, hospitalizations, and systemic immunosuppression. Immuno-oncology trials should routinely report these metrics. Most patients do not tolerate 4 doses of nivo + ipi; however, 4 doses may not be required for clinical benefit.
Author Postow, Michael A
Friedman, Claire F
Wolchok, Jedd D
Chapman, Paul B
Momtaz, Parisa
Shoushtari, Alexander N
Panageas, Katherine S
Navid-Azarbaijani, Pedram
Callahan, Margaret K
Author_xml – sequence: 1
  givenname: Alexander N
  surname: Shoushtari
  fullname: Shoushtari, Alexander N
  organization: Weill Cornell Medical College, New York, New York
– sequence: 2
  givenname: Claire F
  surname: Friedman
  fullname: Friedman, Claire F
  organization: Weill Cornell Medical College, New York, New York
– sequence: 3
  givenname: Pedram
  surname: Navid-Azarbaijani
  fullname: Navid-Azarbaijani, Pedram
  organization: Weill Cornell Medical College, New York, New York
– sequence: 4
  givenname: Michael A
  surname: Postow
  fullname: Postow, Michael A
  organization: Weill Cornell Medical College, New York, New York
– sequence: 5
  givenname: Margaret K
  surname: Callahan
  fullname: Callahan, Margaret K
  organization: Weill Cornell Medical College, New York, New York
– sequence: 6
  givenname: Parisa
  surname: Momtaz
  fullname: Momtaz, Parisa
  organization: Weill Cornell Medical College, New York, New York
– sequence: 7
  givenname: Katherine S
  surname: Panageas
  fullname: Panageas, Katherine S
  organization: Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York
– sequence: 8
  givenname: Jedd D
  surname: Wolchok
  fullname: Wolchok, Jedd D
  organization: Weill Cornell Medical College, New York, New York
– sequence: 9
  givenname: Paul B
  surname: Chapman
  fullname: Chapman, Paul B
  organization: Weill Cornell Medical College, New York, New York
BackLink https://www.ncbi.nlm.nih.gov/pubmed/28817755$$D View this record in MEDLINE/PubMed
BookMark eNpNUNFKwzAADDJxc-4LBMmjL51JmjTNo4xNB5v6UJ9LkiaS0SSzaUX_3qITfLo7uDuOuwSTEIMB4BqjJUYI3x2klzHo2C4JwnxJcoHPwIzknGaEUjb5x6dgkdIBjSnKUUHJBZiSssScMzYD9d7INHQuvMEqfjoN19Ya3ScoQwMr5w3sI6w6I3tvQg830rVDZ6CNHXxyH7EdvFTwpR0S3B5d6_yPdgHuTStD9PIKnFvZJrM44Ry8btbV6jHbPT9sV_e7TI4L-ww3kpUMaaYULRrFONfGMq6oIDZXuRYMK9ZYmbOioJLQRlMrGsKYzjGmSpM5uP3tPXbxfTCpr71L2rTjChOHVGORI8qFEOVovTlZB-VNUx8752X3Vf-dQr4Bmw5otg
CitedBy_id crossref_primary_10_1097_WCO_0000000000000867
crossref_primary_10_1158_1078_0432_CCR_19_1457
crossref_primary_10_36290_far_2019_019
crossref_primary_10_1016_j_ejca_2023_01_034
crossref_primary_10_1080_14712598_2020_1699053
crossref_primary_10_1111_ijd_15163
crossref_primary_10_3389_fphar_2022_989461
crossref_primary_10_1007_s12265_020_09992_5
crossref_primary_10_1007_s40264_023_01357_6
crossref_primary_10_1186_s40425_019_0667_0
crossref_primary_10_7759_cureus_87049
crossref_primary_10_1136_jim_2021_001806
crossref_primary_10_3389_fmed_2018_00351
crossref_primary_10_1016_j_it_2019_04_002
crossref_primary_10_1016_j_semcancer_2022_05_015
crossref_primary_10_1016_j_jconrel_2021_10_013
crossref_primary_10_1080_21645515_2021_1889449
crossref_primary_10_3389_fimmu_2025_1616872
crossref_primary_10_3390_cancers15245707
crossref_primary_10_1186_s40425_018_0346_6
crossref_primary_10_1186_s40425_019_0694_x
crossref_primary_10_1053_j_seminoncol_2019_10_003
crossref_primary_10_1016_j_intimp_2023_109881
crossref_primary_10_1016_j_heliyon_2024_e41597
crossref_primary_10_1097_HC9_0000000000000063
crossref_primary_10_1002_cam4_5438
crossref_primary_10_1016_j_jgo_2018_06_009
crossref_primary_10_1007_s40487_019_0096_8
crossref_primary_10_1158_1078_0432_CCR_20_3449
crossref_primary_10_1016_j_intimp_2020_106628
crossref_primary_10_1002_adtp_202000027
crossref_primary_10_1016_j_omto_2019_03_007
crossref_primary_10_1080_01658107_2019_1566385
crossref_primary_10_3390_cancers17111747
crossref_primary_10_3389_fimmu_2022_860421
crossref_primary_10_1016_j_jid_2021_06_026
crossref_primary_10_1038_s41416_024_02887_1
crossref_primary_10_1016_j_jconrel_2018_06_035
crossref_primary_10_1016_j_critrevonc_2021_103354
crossref_primary_10_1002_cncr_32506
crossref_primary_10_1002_cam4_4076
crossref_primary_10_2174_0109298673283943240227104122
crossref_primary_10_1002_cncr_34004
crossref_primary_10_1097_MED_0000000000000418
crossref_primary_10_1038_s41598_018_37883_y
crossref_primary_10_1016_j_clon_2021_06_009
crossref_primary_10_1016_j_phymed_2023_154765
crossref_primary_10_1002_cam4_4405
crossref_primary_10_1016_j_ejca_2021_04_045
crossref_primary_10_1038_s41568_022_00503_z
crossref_primary_10_1002_adtp_202000055
crossref_primary_10_1016_j_cej_2024_153131
crossref_primary_10_1002_cncr_31889
crossref_primary_10_3390_cancers14102460
crossref_primary_10_1136_annrheumdis_2019_216510
crossref_primary_10_1200_JCO_18_00145
crossref_primary_10_1016_j_cpccr_2020_100044
crossref_primary_10_1002_cam4_70011
crossref_primary_10_3390_cancers14215267
crossref_primary_10_1007_s00345_021_03632_6
crossref_primary_10_3389_fonc_2022_1026978
crossref_primary_10_1016_j_rdc_2020_04_003
crossref_primary_10_1158_1078_0432_CCR_20_4189
crossref_primary_10_1002_art_40745
crossref_primary_10_3390_cancers13122931
crossref_primary_10_1212_CON_0000000000000873
crossref_primary_10_12998_wjcc_v8_i18_4100
crossref_primary_10_1093_oncolo_oyad097
crossref_primary_10_1016_j_toxlet_2024_11_007
crossref_primary_10_1080_14740338_2020_1757068
crossref_primary_10_1016_j_ijrobp_2020_07_2326
crossref_primary_10_1007_s00520_020_05710_8
crossref_primary_10_2217_imt_2021_0082
crossref_primary_10_1371_journal_pone_0255716
crossref_primary_10_3390_vaccines6040079
crossref_primary_10_1186_s12967_023_04784_2
crossref_primary_10_1007_s13671_023_00415_7
crossref_primary_10_1080_09273948_2020_1773867
crossref_primary_10_3390_cancers13215510
crossref_primary_10_3390_cimb47030184
crossref_primary_10_3390_ijms24032769
crossref_primary_10_1136_jitc_2022_005635
crossref_primary_10_1002_jso_26229
crossref_primary_10_1007_s00262_019_02321_z
crossref_primary_10_1200_JCO_19_00508
crossref_primary_10_3390_cancers17121992
crossref_primary_10_1016_j_gore_2025_101955
crossref_primary_10_1200_JCO_18_02141
crossref_primary_10_1016_j_ccc_2020_08_003
crossref_primary_10_1159_000487082
crossref_primary_10_3389_fmed_2022_1014257
crossref_primary_10_1186_s40425_018_0426_7
crossref_primary_10_3322_caac_21596
crossref_primary_10_1007_s00345_021_03716_3
crossref_primary_10_1016_j_jaad_2020_03_132
crossref_primary_10_1186_s13046_022_02568_y
crossref_primary_10_1634_theoncologist_2020_0373
crossref_primary_10_1200_EDBK_280539
crossref_primary_10_1136_jitc_2019_000331
crossref_primary_10_3389_fonc_2022_836859
crossref_primary_10_1002_cncr_32542
crossref_primary_10_1007_s40259_020_00428_9
crossref_primary_10_1038_s41571_020_0352_8
crossref_primary_10_1136_jitc_2024_009061
ContentType Journal Article
DBID CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOI 10.1001/jamaoncol.2017.2391
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: 7X8
  name: MEDLINE - Academic
  url: https://search.proquest.com/medline
  sourceTypes: Aggregation Database
DeliveryMethod no_fulltext_linktorsrc
Discipline Medicine
EISSN 2374-2445
ExternalDocumentID 28817755
Genre Clinical Trial
Journal Article
GrantInformation_xml – fundername: NCI NIH HHS
  grantid: P30 CA008748
GroupedDBID 0R~
53G
ABBLC
ABJNI
ABPMR
ACGFS
ADBBV
ALMA_UNASSIGNED_HOLDINGS
AMJDE
ANMPU
BRYMA
C45
CGR
CUY
CVF
EBS
ECM
EIF
EJD
H13
NPM
NYF
OGEVE
OVD
RAJ
TEORI
7X8
ID FETCH-LOGICAL-a445t-1da5850c5bb46db577cef57b492f3b3c951b5dfa35664a24dc4f9d255c3114bc2
IEDL.DBID 7X8
ISICitedReferencesCount 127
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=000422795300019&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 2374-2445
IngestDate Fri Jul 11 08:15:36 EDT 2025
Thu Jan 02 22:54:07 EST 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-a445t-1da5850c5bb46db577cef57b492f3b3c951b5dfa35664a24dc4f9d255c3114bc2
Notes ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
PMID 28817755
PQID 1930479998
PQPubID 23479
ParticipantIDs proquest_miscellaneous_1930479998
pubmed_primary_28817755
PublicationCentury 2000
PublicationDate 2018-01-01
PublicationDateYYYYMMDD 2018-01-01
PublicationDate_xml – month: 01
  year: 2018
  text: 2018-01-01
  day: 01
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle JAMA oncology
PublicationTitleAlternate JAMA Oncol
PublicationYear 2018
SSID ssj0001470642
Score 2.4738317
Snippet Nivolumab plus ipilimumab (nivo + ipi) is a standard treatment of advanced melanoma. Two randomized trials describe high objective response rates by Response...
SourceID proquest
pubmed
SourceType Aggregation Database
Index Database
StartPage 98
SubjectTerms Adult
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Compassionate Use Trials
Disease Progression
Disease-Free Survival
Drug-Related Side Effects and Adverse Reactions - epidemiology
Female
Humans
Incidence
Ipilimumab - administration & dosage
Ipilimumab - adverse effects
Male
Melanoma - drug therapy
Melanoma - epidemiology
Melanoma - pathology
Middle Aged
Nivolumab - administration & dosage
Nivolumab - adverse effects
Prospective Studies
Skin Neoplasms - drug therapy
Skin Neoplasms - epidemiology
Skin Neoplasms - pathology
Time Factors
Treatment Failure
Young Adult
Title Measuring Toxic Effects and Time to Treatment Failure for Nivolumab Plus Ipilimumab in Melanoma
URI https://www.ncbi.nlm.nih.gov/pubmed/28817755
https://www.proquest.com/docview/1930479998
Volume 4
WOSCitedRecordID wos000422795300019&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText
inHoldings 1
isFullTextHit
isPrint
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1LS8NAEF7Uinjx_agvVvC6arK72eQkIhY9JPRQobewr0CgTappxZ_v7CalIAiCl0AOgTD5MvPNN7MzCN04-R6wYUmoCk1YpBkBVi9JohMIMDELAs38sgmRZfF4nAw7wa3p2iqXPtE7alNrp5HfAdFw09AhO3iYvRO3NcpVV7sVGuuoR4HKOFSLcbzSWJhw_NrvlxOMQCTjPwYP1RWY2zV4iduQJsHvNNOHm8Huf190D-10RBM_tsjYR2u2OkBbaVdKP0R56tVBiFx4VH-VGrdzjBssK4PdwRA8r_Fo2YaOB7J0DewYOC7OSu_TpMLDyaLBr7NyUk79fVnh1E5kVU_lEXobPI-eXki3bYFIsMucBEZC6nCvuVIsMooLoW3BhWJJWFBFNVAxxU0hKRBAJkNmNCsSAxmJppBTKR0eo42qruwpwpRaERpmaJTEEO8ixWkRhSJy5E_YWPbR9dJ0OaDZlShkZetFk6-M10cnrf3zWTt2Iw_jOBCC87M_PH2OtuGjxq1WcoF6BfzL9hJt6s952XxceZjANRum31E7xlg
linkProvider ProQuest
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Measuring+Toxic+Effects+and+Time+to+Treatment+Failure+for+Nivolumab+Plus+Ipilimumab+in+Melanoma&rft.jtitle=JAMA+oncology&rft.au=Shoushtari%2C+Alexander+N&rft.au=Friedman%2C+Claire+F&rft.au=Navid-Azarbaijani%2C+Pedram&rft.au=Postow%2C+Michael+A&rft.date=2018-01-01&rft.issn=2374-2445&rft.eissn=2374-2445&rft.volume=4&rft.issue=1&rft.spage=98&rft_id=info:doi/10.1001%2Fjamaoncol.2017.2391&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2374-2445&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2374-2445&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2374-2445&client=summon