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Management of Immune-Related Adverse Events and Kinetics of Response With Ipilimumab
Abstract
Monoclonal antibodies directed against the immune checkpoint protein cytotoxic T-lymphocyte antigen-4 (CTLA-4; CD152)—ipilimumab and tremelimumab—have been investigated in metastatic melanoma and other cancers and have shown promising results. Recently, ipilimumab was approved by the US Food and Drug Administration for the treatment of metastatic melanoma. We review the literature on managing the adverse effects and kinetics of tumor regression with ipilimumab and provide guidelines on their management. During treatment with these antibodies, a unique set of adverse effects may occur, called immune-related adverse events (irAEs). These include rashes, which may rarely progress to life-threatening toxic epidermal necrolysis, and colitis, characterized by a mild to moderate, but occasionally also severe and persistent diarrhea. Hypophysitis, hepatitis, pancreatitis, iridocyclitis, lymphadenopathy, neuropathies, and nephritis have also been reported with ipilimumab. Early recognition of irAEs and initiation of treatment are critical to reduce the risk of sequelae. Interestingly, irAEs correlated with treatment response in some studies. Unique kinetics of response have been observed with CTLA-4 blockade with at least four patterns: (1) response in baseline lesions by week 12, with no new lesions seen; (2) stable disease, followed by a slow, steady decline in total tumor burden; (3) regression of tumor after initial increase in total tumor burden; and (4) reduction in total tumor burden during or after the appearance of new lesion(s) after week 12. We provide a detailed description of irAEs and recommendations for practicing oncologists who are managing them, along with the unusual kinetics of response associated with ipilimumab therapy.
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“We observed an association between irAEs and improved PFS using a landmark analysis, in agreement with previous studies58–60, and uncovered that baseline gut microbiome composition segregated PD-1-treated patients who developed irAEs from those who did not.”
From Intestinal microbiota signatures of clinical response and immune-related adverse events in melanoma patients treated with anti-PD-1 (2022) · cites this paper as [60]
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“Any irAEs would generally emerge before the last dose of the treatment course, although hepatitis and endocrinopathies have been reported after the last dose of drug.(70) Table 2.”
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“32 In addition, irAEs may occur up to 6 months after discontinuation of ICIs, 33 and 28.8% of ICI-rechallenged patients experience the same irAEs associated with the discontinuation of ICIs.”
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“Symptomatic patients require timely treatment with steroids (and ongoing physiological steroid replacement) and then replacement of any other relevant pituitary hormone axis affected.(14,15) Adrenal crisis might ensue and urgent i.”
BackgroundInfluentialAfzal, M. Z., Mabaera, R., & Shirai, K. (2018) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-018-0322-1 · Cited by 33
Efficacy and side effects of immune checkpoint inhibitors in the treatment of colorectal cancer
Manz, S., Losa, M., Fritsch, R., & Scharl, M. M. (2021) · Therapeutic Advances in Gastroenterology · doi:10.1177/17562848211002018 · Cited by 36
Suzuki, S., Suzuki, S., Shibata, K., Shibata, K., Kikkawa, F., Kikkawa, F., Nakatsura, T., & Nakatsura, T. (2013) · Human Vaccines & Immunotherapeutics · doi:10.4161/hv.27217 · Cited by 33
Cutaneous toxicities of new treatments for melanoma
Boada, A., Carrera, C., Segura, S., Collgros, H., Pasquali, P., Bodet, D., Puig, S., & Malvehy, J. (2018) · Clinical & Translational Oncology · doi:10.1007/s12094-018-1891-7 · Cited by 33
Allen, K. J. H., Jiao, R., Malo, M. E., Frank, C., Fisher, D. R., Rickles, D. J., & Dadachova, E. (2019) · Pharmaceutics · doi:10.3390/pharmaceutics11070348 · Cited by 33
“Unfortunately, only a small amount of patients respond well to the current immune therapies, coupled with very serious side effects and the large cost of these treatments [9,10] there is still a high demand for additional approaches to combat metastatic melanoma that can either stand alone or as a combination therapeu…”
BackgroundImmune checkpoint inhibitors and acute kidney injury
Zhou, P., Gao, Y., Kong, Z., Wang, J., Si, S., Han, W., Li, J., Lv, Z., & Wang, R. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1353339 · Cited by 33
“As examples, the common dermatitis usually develops within 4 weeks (44, 66, 67) and colitis within 6 weeks after ICIs treatment (43).”
BackgroundInfluentialKroemer, G., & Galluzzi, L. (2015) · OncoImmunology · doi:10.1080/2162402x.2015.1058037 · Cited by 32
Cytotoxic T-Lymphocyte Antigen-4 Blockade in Melanoma
Buchbinder, E. I., & McDermott, D. F. (2015) · Clinical Therapeutics · doi:10.1016/j.clinthera.2015.02.003 · Cited by 32
Expert opinion on pituitary complications in immunotherapy
Briet, C., Albarel, F., Kuhn, E., Merlen, E., Chanson, P., & Cortet, C. (2018) · Annales d Endocrinologie · doi:10.1016/j.ando.2018.07.008 · Cited by 32
Cell-targeted c(AmpRGD)-sunitinib molecular conjugates impair tumor growth of melanoma
Bianchini, F., Portioli, E., Ferlenghi, F., Vacondio, F., Andreucci, E., Biagioni, A., Ruzzolini, J., Peppicelli, S., Lulli, M., Calorini, L., et al. (2019) · Cancer Letters · doi:10.1016/j.canlet.2018.12.021 · Cited by 32
“), many concerns still exist dealing with the observed overall toxicity [19,20], the effective dosing regimens and, above all, the insurgence of resistance mechanisms leading to tumor relapse and progression to a metastatic disease with incredibly aggressive features [21].”
BackgroundKamińska‐Winciorek, G., Cybulska-Stopa, B., Lugowska, I. A., Ziobro, M., & Rutkowski, P. L. (2019) · Advances in Dermatology and Allergology · doi:10.5114/ada.2018.80272 · Cited by 32
Characteristics and risk factors for microbial infections during cancer immune checkpoint therapy
Kanjanapan, Y., & Yip, D. (2020) · Cancer Medicine · doi:10.1002/cam4.3532 · Cited by 32
“Treatment duration Cycles received 7 (1-98) 5 (1-71) 0.”
BackgroundSanaei, M., Pourbagheri‐Sigaroodi, A., Kaveh, V., Sheikholeslami, S. A., Salari, S., & Bashash, D. (2020) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2020.103160 · Cited by 34
NLRC5/CITA expression correlates with efficient response to checkpoint blockade immunotherapy
Yoshihama, S., Cho, S., Yeung, J., Pan, X., Lizee, G. A., Konganti, K., Johnson, V. E., & Kobayashi, K. S. (2021) · Scientific Reports · doi:10.1038/s41598-021-82729-9 · Cited by 32
Cunningham, M. E., Iafolla, M. A. J., Kanjanapan, Y., Cerocchi, O., Butler, M. O., Siu, L. L., Bedard, P. L., Ross, K., Hansen, B. E., Spreafico, A., et al. (2021) · PLoS ONE · doi:10.1371/journal.pone.0253070 · Cited by 33
“6%) was comparable with other published data [1, 4, 15, 16].”
ResultThe Underestimated and Overlooked Burden of Diarrhea and Constipation in Cancer Patients
Moschen, A. R., Sammy, Y., Marjenberg, Z. R., Heptinstall, A. B., Pooley, N., & Marczewska, A. M. (2022) · Current Oncology Reports · doi:10.1007/s11912-022-01267-3 · Cited by 35
Nivolumab plus ipilimumab combination therapy in cancer: Current evidence to date
Nikoo, M., Rabiee, F., Mohebbi, H., Eghbalifard, N., Rajabi, H., Yazdani, Y., Sakhaei, D., Khosravifarsani, M., & Akhavan‐Sigari, R. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.109881 · Cited by 33
Demlová, R., Valík, D., Obermannova, R. L., & Dubská, L. Z. (2016) · Physiological Research · doi:10.33549/physiolres.933525 · Cited by 32
Biologic response modifiers: Indications, implications, and insights
Davis, B. P., & Ballas, Z. K. (2017) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2017.02.013 · Cited by 31
The 100 top-cited studies in cancer immunotherapy
Zhang, Y., Quan, L., & Du, L. (2019) · Artificial Cells Nanomedicine and Biotechnology · doi:10.1080/21691401.2019.1623234 · Cited by 31
“Management of immune-related adverse events and kinetics of response with ipilimumab [94] Journal of Clinical Oncology Review 642 2012 7 22614989”
BackgroundHardy, T., Yin, M., Chavez, J. A., Ivanov, I., Chen, W., Nádasdy, T., & Brodsky, S. V. (2020) · Cardiovascular Pathology · doi:10.1016/j.carpath.2020.107202 · Cited by 31
Re-introducing immunotherapy in patients surviving immune checkpoint inhibitors-mediated myocarditis
Hasson, S. P., Salwen, B., Sivan, A., Shamai, S., Geva, R., Merimsky, O., Raphael, A., Shmilovich, H., Moshkovits, Y., Kapusta, L., et al. (2020) · Clinical Research in Cardiology · doi:10.1007/s00392-020-01648-3 · Cited by 32
“Some of the commonly characterized toxicities are rash, diarrhea, colitis, and hypophysitis [10], however, myocarditis was not identified as an ICI-mediated adverse event in pivotal trials [11–13].”
BackgroundYeung, S. J., Qdaisat, A. Z., Chaftari, P. S., Lipe, D. N., Merlin, J., Rajha, E., Wechsler, A. H., Sandoval, M., Viets-Upchurch, J. M., Al‐Breiki, A., et al. (2020) · Journal of the American College of Emergency Physicians Open · doi:10.1002/emp2.12209 · Cited by 29
Hepatitis B Virus Reactivation in Cancer Patients Treated With Immune Checkpoint Inhibitors
Burns, E. A., Muhsen, I. N., Anand, K., Xu, J., Umoru, G., Arain, A., & Abdelrahim, M. (2021) · Journal of Immunotherapy · doi:10.1097/cji.0000000000000358 · Cited by 31
Hyperacute toxicity with combination ipilimumab and anti-PD1 immunotherapy
Dearden, H. C., Au, L., Wang, D. Y., Zimmer, L., Eroglu, Z., Smith, J. L., Cuvietto, M., Khoo, C. C. H., Atkinson, V. G., Lo, S., et al. (2021) · European Journal of Cancer · doi:10.1016/j.ejca.2021.04.045 · Cited by 31
Harnessing the immune system by targeting immune checkpoints: Providing new hope for Oncotherapy
Yu, L., Sun, M., Zhang, Q., Zhou, Q., & Wang, Y. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.982026 · Cited by 32
Management of adverse events related to new cancer immunotherapy (immune checkpoint inhibitors)
Bourke, J., O'Sullivan, M. D., & Khattak, M. A. (2016) · The Medical Journal of Australia · doi:10.5694/mja16.00586 · Cited by 31
Bastiaannet, E., Battisti, N. M. L., Loh, K. P., de Glas, N. A., Soto‐Pérez‐de‐Celis, E., Baldini, C., Kapiteijn, E., & Lichtman, S. M. (2018) · Journal of Geriatric Oncology · doi:10.1016/j.jgo.2018.06.009 · Cited by 31
“Approximately 20–30% of the adverse events were grade 3–4 [32].”
Background
Metadata
- Authors
- Weber, J. S., Kähler, K. C., & Hauschild, A.
- Affiliations
- Moffitt Cancer Center (US)
- Venue
- Journal of Clinical Oncology
- Published
- 2012-07-20
- Volume
- 30
- Issue
- 21
- Pages
- 2691-2697
- ISSN
- 0732-183X (ISSN-L)
- 1527-7755
- OpenAlex
- W2109653150
- Cited by
- 1,415
- References
- 33
- Citations by year
- 2026: 24 · 2025: 35 · 2024: 59 · 2023: 79 · 2022: 84 · 2021: 117 · 2020: 129 · 2019: 123 · 2018: 146 · 2017: 153 · 2016: 152 · 2015: 145 · 2014: 94 · 2013: 65 · 2012: 9
- FWCI
- 10.34
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Clinical Oncology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Health Sciences › Medicine › Oncology › Cutaneous Melanoma Detection and Management
- Keywords
- ipilimumab, immune-related adverse events, CTLA-4 blockade, metastatic melanoma, immune checkpoint inhibitors, toxic epidermal necrolysis, colitis, hypophysitis, hepatitis, iridocyclitis, neuropathy, nephritis, adverse event management
- MeSH terms
- Ipilimumab, Antibodies, Monoclonal, Antineoplastic Agents, Colitis, Drug Eruptions, Diarrhea, Humans, Liver, Lymphatic Diseases, Melanoma, Mucous Membrane, Pancreatitis, Peripheral Nervous System Diseases, Pituitary Gland, Skin, Skin Neoplasms, Stevens-Johnson Syndrome, Uveitis, Scleritis, Chemical and Drug Induced Liver Injury, CTLA-4 Antigen, Antibodies, Monoclonal, Humanized
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