Cited by 77Ultrasound and Hyperthermia ApplicationsMicrobial Inactivation MethodsNonmelanoma Skin Cancer Studies

Cryoablation: physical and molecular basis with putative immunological consequences

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Baust, John G., Snyder, Kristi K., Santucci, Kimberly L., Robilotto, Anthony T., Van Buskirk, Robert G., Baust, John M.·2019·International Journal of Hyperthermia

Abstract

that impacts all cellular processes. CA is independent of cell cycle stage and degree of cellular stemness. Importantly, CA is typically applied as a non-repetitive (single session) treatment that does not support adaptative mutagenesis as do many repetitive therapies. CA is characterized by the launch of multiple forms of cell death including (a) ice-related physical damage, (b) initiation of cellular stress responses (kill switch activation) and launch of necrosis and apoptosis, (c) vascular stasis, and (d) likely activation of ablative immune responses. CA is not without limitation related to the thermal gradient formed between cryoprobe surface (∼-185°C) and the distal surface of the freeze zone (∼0°C) requiring freeze margin extension beyond the tumor boundary (up to ∼1 cm). This limitation is mitigated in part by commonly applied dual freeze thaw cycles and the use of freeze sensitizing adjuvants. This review will (1) identify the cascade of damaging effects of the freeze-thaw process, its physical and molecular-based relationships, (2) a likely immunological involvement (abscopic effect), and (3) explore the use of freeze-sensitizing adjuvants necessary to limit freezing beyond the tumor margin.

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Crossref · 10.1080/02656736.2019.1647355

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  • Clinical outcomes of tumor cryoablation-both obtaining local control and achieving an abscopal effect-are highly unpredictable with variable magnitudes of response and frequent failure of local recurrence.

    “Despite these theoretical benefits, clinical outcomes of tumor cryoablation—both obtaining local control and achieving an abscopal effects—are highly unpredictable with variable magnitudes of response and frequent failure of local recurrence.”

    From Functional tumor cell-intrinsic STING, not host STING, drives local and systemic antitumor immunity and therapy efficacy following cryoablation (2023) · cites this paper as [78]

    The Cryo-immunological Responses section (page unavailable) says distant-tumor effects are not always observed, are transient, and vary in extent; the Introduction says freezing does not damage a targeted tumor uniformly. These passages support variable responses, but they do not establish that clinical local control is highly unpredictable or that local recurrence frequently occurs. (LLM, conf=0.84)

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Research works printed but not linked: 7

  1. [1]Baust JG, Bischof J, Jiang-Hughes J, Polascik T, Rukstalis D, Corwin W, Gage AA, Baust JM. Re-purposing Thermal Ablative Therapies. Nature’s Prostate Cancer & Prostatic Diseases. 2015 18(2): 87– 95. 25622539
  2. [3]Hollister WR, Mathew AJ, Baust JG, Van Buskirk RG. Effects of freezing on cell viability and mechanisms of cell death in a human prostate cancer cell line. Molecular Urology. 1998 2(1): 13– 8.
  3. [4]Clarke D, Baust JM, Van Buskirk RG, Baust JG. Addition of Anti-cancer Agents Enhances Freezing-induced Prostate Cancer Cell Death: Implication of Mitochondrial Involvement. Cryobiology. 2004 49(1): 45– 61. 15265716
  4. [5]Robilotto AT, Baust JM, Van Buskirk RG, Gage AA, Baust JG. Temperature Dependent Apoptotic Pathway Activation During Cryoablation. Prostate Cancer & Prostatic Diseases 2013 16: 41– 49. 23229563
  5. [11]Shulman S, Brandt EJ, Yantoto C. Studies in cryoimmunology II. Tissue and species speificity of auto-antibody response and comparison with iso-immunization. Immunology. 1968 14: 149– 158. 4966655 PMC1409294
  6. [12]Soanes WA, Ablin RJ, Gonder MJ Remission of metastatic lesions following cryosurgery in prostatic cancder. J. Urology. 1970 104: 154– 159. 4987666
  7. [53]Baust JG, Gage AA, Bjerklund Johansen TE, Baust JM. Mechanisms of cryoablation: clinical consequences on malignant tumors. Cryobiology. 2014 2; 68(1): 1– 11. 24239684 PMC3976170

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Authors
Baust, J. G., Snyder, K. K., Santucci, K. L., Robilotto, A. T., Van Buskirk, R. G., & Baust, J. M.
Affiliations
  • Binghamton University (US)
  • Cell Preservation Services (United States) (US)
  • State University of New York, Binghamton, NY, USA;
Corresponding author
Baust, John G.
Venue
International Journal of Hyperthermia
Published
2019-11-29
Volume
36
Issue
sup1
Pages
10-16
ISSN
  • 0265-6736 (ISSN-L)
  • 1464-5157
OpenAlex
W2992532374
Cited by
76
References
52
Citations by year
2026: 14 · 2025: 15 · 2024: 10 · 2023: 16 · 2022: 8 · 2021: 7 · 2020: 6
FWCI
0.42
Type
journal article
Language
en
Open access
Locations
  • International Journal of Hyperthermia (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • National Institutes of Health (1r43ca210761-01a1)
  • National Cancer Institute (R44CA183265, R43CA183265, R43 CA210761)
Topics
  • Physical Sciences › Engineering › Biomedical Engineering › Ultrasound and Hyperthermia Applications
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Microbial Inactivation Methods
  • Health Sciences › Medicine › Epidemiology › Nonmelanoma Skin Cancer Studies
Keywords
cryoablation, frost damage, ice formation, cellular stress response, necrosis, apoptosis, vascular stasis, abscopal effect, temperature gradient, tumor margin, cancer immunotherapy
MeSH terms
Cryosurgery, Humans

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