Vaccimel immunization is associated with enhanced response to treatment with anti-PD-1 monoclonal antibodies in cutaneous melanoma patients - a case reports study

Front Immunol. 2024 Apr 25:15:1354710. doi: 10.3389/fimmu.2024.1354710. eCollection 2024.

Abstract

Cancer vaccines are gaining ground as immunotherapy options. We have previously demonstrated in cutaneous melanoma (CM) patients that adjuvant treatment with VACCIMEL, a mixture of four irradiated CM cell lines co-adjuvanted with BCG and GM-CSF, increases the cellular immune response to melanocyte differentiation antigens, cancer-testis antigens and neoantigens, with respect to basal levels. On the other hand, it is also known that treatment with anti-PD-1 monoclonal antibodies (MAbs), acting on pre-existing tumor-reactive lymphocytes, induces clinical responses in CM patients, albeit in a fraction of treated patients. A combination of both treatments would appear therefore desirable. In this paper, we describe CM patients who, having progressed even years after vaccination, were treated with anti-PD-1 MAbs. In 5/5 of such progressor patients, complete responses were obtained which lasted between 3 and 65+ months. Three of the patients remain disease-free and two recurred. One of the patients passed away after a recurrence of brain metastases. We suggest that clonally expanded reactive lymphocytes induced by VACCIMEL partially remain as memory cells, which may be recalled after tumor recurrence and may foster ulterior activity of anti-PD-1 MAbs.

Keywords: case report; cutaneous melanoma; immune checkpoints inhibitors; immunotherapy; vaccine.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Immunologic / administration & dosage
  • Adjuvants, Immunologic / therapeutic use
  • Aged
  • Antibodies, Monoclonal / therapeutic use
  • Cancer Vaccines* / administration & dosage
  • Cancer Vaccines* / immunology
  • Cancer Vaccines* / therapeutic use
  • Female
  • Humans
  • Immune Checkpoint Inhibitors / therapeutic use
  • Male
  • Melanoma* / drug therapy
  • Melanoma* / immunology
  • Melanoma* / therapy
  • Melanoma, Cutaneous Malignant
  • Middle Aged
  • Programmed Cell Death 1 Receptor* / antagonists & inhibitors
  • Programmed Cell Death 1 Receptor* / immunology
  • Skin Neoplasms* / drug therapy
  • Skin Neoplasms* / immunology
  • Skin Neoplasms* / therapy
  • Treatment Outcome

Substances

  • Programmed Cell Death 1 Receptor
  • Cancer Vaccines
  • PDCD1 protein, human
  • Immune Checkpoint Inhibitors
  • Antibodies, Monoclonal
  • Adjuvants, Immunologic

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by grants from Agreement SALES Foundation-CONICET Argentina, 1883/98; National Cancer Institute-National Ministry of Health from Argentina (INC-MSal), INC III-IS001946; Agencia I+D Argentina, PICT-2021-I-A-00733; Cancer Foundation (FUCA) Argentina, Annual Grant 2023-2024; and Pedro F. Mosoteguy Foundation Argentina, Annual Grant 2023-2024. The CASVAC-0401 clinical study was sponsored by Laboratorio Pablo Cassará S.R.L. Laboratorio Pablo Cassará was not involved in the study design, collection, analysis, interpretation of data, the writing of this article or the decision to submit it for publication.