Assessing Ipilimumab Targeting CTLA-4 for Metastatic Melanoma Treatment: Surgical Perspectives
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Abstract
Abstract
Ipilimumab treatment demonstrates significant tumor responses in patients battling metastatic melanoma. Our study examines 179 assessable patients across three clinical trials, with long-term follow-up aimed at gauging response sustainability. Patients, enrolled between 2015 and 2022, underwent treatment across three protocols: Protocol 1 involved ipilimumab combined with gp100 peptides for fifty-six patients, Protocol 2 utilized ipilimumab with interleukin-2 for thirty-six patients, and Protocol 3 administered ipilimumab with intra-patient dose escalation and randomized gp100 peptide administration for eighty-five patients. Analysis of their extended follow-up and survival metrics reveals compelling insights. Median follow-up durations for Protocols 1, 2, and 3 were 92, 84, and 71 months, respectively. Median survival rates stood at 14, 16, and 13 months, with corresponding five-year survival rates of 13%, 25%, and 23%. Protocol 2 demonstrated a notable 17% complete response (CR) rate, surpassing Protocol 1 (7%) and Protocol 3 (6%). These rates, higher than previously documented, underscore sustained tumor regression over months to years’ post-therapy. Remarkably, nearly all complete responders (15 out of 16) remain in remission for 54+ to 99+ months. This study presents the most extensive follow-up data for melanoma patients treated with ipilimumab, affirming its potential to induce enduring, potentially curative tumor regression in select metastatic melanoma cases. Notably, the combination of ipilimumab and IL-2 demonstrates an elevated CR rate, warranting further investigation through randomized trials.
Ipilimumab treatment demonstrates significant tumor responses in patients battling metastatic melanoma. Our study examines 179 assessable patients across three clinical trials, with long-term follow-up aimed at gauging response sustainability. Patients, enrolled between 2015 and 2022, underwent treatment across three protocols: Protocol 1 involved ipilimumab combined with gp100 peptides for fifty-six patients, Protocol 2 utilized ipilimumab with interleukin-2 for thirty-six patients, and Protocol 3 administered ipilimumab with intra-patient dose escalation and randomized gp100 peptide administration for eighty-five patients. Analysis of their extended follow-up and survival metrics reveals compelling insights. Median follow-up durations for Protocols 1, 2, and 3 were 92, 84, and 71 months, respectively. Median survival rates stood at 14, 16, and 13 months, with corresponding five-year survival rates of 13%, 25%, and 23%. Protocol 2 demonstrated a notable 17% complete response (CR) rate, surpassing Protocol 1 (7%) and Protocol 3 (6%). These rates, higher than previously documented, underscore sustained tumor regression over months to years’ post-therapy. Remarkably, nearly all complete responders (15 out of 16) remain in remission for 54+ to 99+ months. This study presents the most extensive follow-up data for melanoma patients treated with ipilimumab, affirming its potential to induce enduring, potentially curative tumor regression in select metastatic melanoma cases. Notably, the combination of ipilimumab and IL-2 demonstrates an elevated CR rate, warranting further investigation through randomized trials.
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Dr Keshav Ladda, D. A. A. P. , D. H. V. N. ,. (2024). Assessing Ipilimumab Targeting CTLA-4 for Metastatic Melanoma Treatment: Surgical Perspectives. Obstetrics and Gynaecology Forum, 34(3s), 1021–1027. Retrieved from https://obstetricsandgynaecologyforum.com/index.php/ogf/article/view/413
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