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Impact of immediate cryopreservation on the establishment of patient derived xenografts from head and neck cancer patients
Impact of immediate cryopreservation on the establishment of patient derived xenografts from head and neck cancer patients
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Impact of immediate cryopreservation on the establishment of patient derived xenografts from head and neck cancer patients
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Impact of immediate cryopreservation on the establishment of patient derived xenografts from head and neck cancer patients
Impact of immediate cryopreservation on the establishment of patient derived xenografts from head and neck cancer patients

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Impact of immediate cryopreservation on the establishment of patient derived xenografts from head and neck cancer patients
Impact of immediate cryopreservation on the establishment of patient derived xenografts from head and neck cancer patients
Journal Article

Impact of immediate cryopreservation on the establishment of patient derived xenografts from head and neck cancer patients

2021
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Overview
Background Patient-derived xenografts established from human cancers are important tools for investigating novel anti-cancer therapies. Establishing PDXs requires a significant investment and many PDXs may be used infrequently due to their similarity to existing models, their growth rate, or the lack of relevant mutations. We performed this study to determine whether we could efficiently establish PDXs after cryopreservation to allow molecular profiling to be completed prior to implanting the human cancer. Methods Fresh tumor was split with half used to establish a PDX immediately and half cryopreserved for later implantation. Resulting tumors were assessed histologically and tumors established from fresh or cryopreserved tissues compared as to the growth rate, extent of tumor necrosis, mitotic activity, keratinization, and grade. All PDXs were subjected to short tandem repeat testing to confirm identity and assess similarity between methods. Results Tumor growth was seen in 70% of implanted cases. No growth in either condition was seen in 30% of tumors. One developed a SCC from the immediate implant but a lymphoproliferative mass without SCC from the cryopreserved specimen. No difference in growth rate was seen. No difference between histologic parameters was seen between the two approaches. Conclusions Fresh human cancer tissue can be immediately cryopreserved and later thawed and implanted to establish PDXs. This resource saving approach allows for tumor profiling prior to implantation into animals thus maximizing the probability that the tumor will be utilized for future research.