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Experimental Melanoma Immunotherapy Model Using Tumor Vaccination with a Hematopoietic Cytokine
Published on: February 24, 2023
Neoadjuvant checkpoint inhibitor immunotherapy for resectable mucosal melanoma
Joel Ho1, Jane Mattei2, Michael Tetzlaff3
1Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Background:
Neoadjuvant checkpoint inhibition (CPI) has recently demonstrated impressive outcomes in patients with stage 3 cutaneous melanoma. However, the safety, efficacy, and outcome of neoadjuvant CPI in patients with mucosal melanoma (MM) are not well studied as MM is a rare melanoma subtype. CPI such as combination nivolumab and ipilimumab achieves response rates of 37-43% in unresectable or metastatic MM but there is limited data regarding the efficacy of these agents in the preoperative setting. We hypothesize that neoadjuvant CPI is a safe and feasible approach for patients with resectable MM.
Method:
Under an institutionally approved protocol, we identified adult MM patients with resectable disease who received neoadjuvant anti-PD1 +/- anti-CTLA4 between 2015 to 2019 at our institution. Clinical information include age, gender, presence of nodal involvement or satellitosis, functional status, pre-treatment LDH, tumor mutation status, and treatment data was collected. Outcomes include event free survival (EFS), overall survival (OS), objective response rate (ORR), pathologic response rate (PRR), and grade ≥3 toxicities.
Results:
We identified 36 patients. Median age was 62; 58% were female. Seventy-eight percent of patients received anti-PD1 + anti-CTLA4. Node positive disease or satellite lesions was present at the time of treatment initiation in 47% of patients. Primary sites of disease were anorectal (53%), urogenital (25%), head and neck (17%), and esophageal (6%). A minority of patients did not undergo surgery due to complete response (n=3, 8%) and disease progression (n=6, 17%), respectively. With a median follow up of 37.9 months, the median EFS was 9.2 months with 3-year EFS rate of 29%. Median OS had not been reached and 3-year OS rate was 55%. ORR was 47% and PRR was 35%. EFS was significantly higher for patients with objective response and for patients with pathologic response. OS was significantly higher for patients with pathologic response. Grade 3 toxicities were reported in 39% of patients.
Conclusion:
Neoadjuvant CPI for resectable MM is a feasible approach with signs of efficacy and an acceptable safety profile. As there is currently no standard approach for resectable MM, this study supports further investigations using neoadjuvant therapy for these patients.
Insights
Neoadjuvant checkpoint inhibition (CPI) is a safe and effective treatment for resectable mucosal melanoma (MM). This approach shows promising efficacy and an acceptable safety profile for patients with this rare melanoma subtype.
Area of Science:
- Oncology
- Dermatology
- Immunotherapy
Background:
- Mucosal melanoma (MM) is a rare subtype with limited research on neoadjuvant therapies.
- Cutaneous melanoma has shown positive outcomes with neoadjuvant checkpoint inhibition (CPI).
- Current data on CPI for unresectable or metastatic MM shows response rates of 37-43%.
Purpose of the Study:
- To evaluate the safety and efficacy of neoadjuvant CPI in patients with resectable mucosal melanoma.
- To determine the feasibility of using CPI in the preoperative setting for MM.
- To assess event-free survival (EFS), overall survival (OS), objective response rate (ORR), and pathologic response rate (PRR).
Main Methods:
- Retrospective analysis of 36 adult MM patients receiving neoadjuvant anti-PD1 +/- anti-CTLA4 from 2015-2019.
- Collection of clinical data including demographics, disease characteristics, and treatment details.
- Evaluation of outcomes such as EFS, OS, ORR, PRR, and grade ≥3 toxicities.
Main Results:
- Median follow-up was 37.9 months; 3-year EFS rate was 29% and 3-year OS rate was 55%.
- Objective response rate (ORR) was 47% and pathologic response rate (PRR) was 35%.
- Grade 3 toxicities occurred in 39% of patients; EFS and OS were significantly higher for patients with objective and pathologic response.
Conclusions:
- Neoadjuvant CPI is a feasible approach for resectable MM, demonstrating efficacy and an acceptable safety profile.
- This study supports further investigation of neoadjuvant therapy for resectable MM, given the lack of a standard approach.
- Neoadjuvant CPI offers a promising treatment option for patients with resectable mucosal melanoma.
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