Complete ablation of small squamous cell carcinoma xenografts with186Re-labeled monoclonal antibody E48

Martijn Gerretsen, Gerard W M Visser, Ruud H. Brakenhoff, Marijke van Walsum, Gordon B. Snow, Guus A M S van Dongen

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

In previous studies we have shown that in mice bearing head and neck squamous cell carcinoma (HNSCC) xenografts, radioimmunotherapy (RIT) with186Re-labeled MAb E48 resulted in complete regressions in one-third of the tumors (followup >150 d). MAb E48 was labeled with186Re following a novel labeling procedure developed at our institute. The injected dose was 600 μCi, which was the maximum tolerated dose (MTD; <15% wt loss) in these studies. The mean size of the tumors was 140±60 mm3. To investigate whether the therapeutic efficacy of RIT in our xenograft model would be improved when treating smaller xenografts, mice bearing 2 HNSCC xenografts with a vol of 75±17 mm3 (number of mice, n=6; number of tumors, t=12) were treated with 600 μCi of186Re-labeled MAb E48 IgG. All tumors completely regressed and did not regrow during followup (>150 d). In all mice, weight loss did not exceed 10%. to obtain biodistribution data, mice bearing two xenografts with a vol of 58±31 mm3 were injected with 100 μCi of186Re-labeled MAb E48 IgG. The maximum uptake in blood was 26.4% injected dose/g (%ID·g-1) at 2 h pi and was 53.1%ID·g-1 in the tumor at d 7 pi. In normal tissues, no nonspecific accumulation was observed. Based on these biodistribution data, the absorbed cumulative radiation dose was calculated. The accumulated dose in blood and tumor was 2004 cGy and 8580 cGy, respectively. In other tissues, the dose was less than 8.1% of the dose delivered to tumor. These data implicate that RIT with186Re-labeled MAb E48 may be especially suited to be used as adjuvant therapy for the treatment of head and neck cancer patients with minimal residual disease.

Original languageEnglish
Pages (from-to)135-142
Number of pages8
JournalCell Biophysics
Volume24-25
Issue number1-3
DOIs
Publication statusPublished - 1 Jan 1994

Cite this

@article{e66b7954fde946149ebf7e89604b5a7b,
title = "Complete ablation of small squamous cell carcinoma xenografts with186Re-labeled monoclonal antibody E48",
abstract = "In previous studies we have shown that in mice bearing head and neck squamous cell carcinoma (HNSCC) xenografts, radioimmunotherapy (RIT) with186Re-labeled MAb E48 resulted in complete regressions in one-third of the tumors (followup >150 d). MAb E48 was labeled with186Re following a novel labeling procedure developed at our institute. The injected dose was 600 μCi, which was the maximum tolerated dose (MTD; <15{\%} wt loss) in these studies. The mean size of the tumors was 140±60 mm3. To investigate whether the therapeutic efficacy of RIT in our xenograft model would be improved when treating smaller xenografts, mice bearing 2 HNSCC xenografts with a vol of 75±17 mm3 (number of mice, n=6; number of tumors, t=12) were treated with 600 μCi of186Re-labeled MAb E48 IgG. All tumors completely regressed and did not regrow during followup (>150 d). In all mice, weight loss did not exceed 10{\%}. to obtain biodistribution data, mice bearing two xenografts with a vol of 58±31 mm3 were injected with 100 μCi of186Re-labeled MAb E48 IgG. The maximum uptake in blood was 26.4{\%} injected dose/g ({\%}ID·g-1) at 2 h pi and was 53.1{\%}ID·g-1 in the tumor at d 7 pi. In normal tissues, no nonspecific accumulation was observed. Based on these biodistribution data, the absorbed cumulative radiation dose was calculated. The accumulated dose in blood and tumor was 2004 cGy and 8580 cGy, respectively. In other tissues, the dose was less than 8.1{\%} of the dose delivered to tumor. These data implicate that RIT with186Re-labeled MAb E48 may be especially suited to be used as adjuvant therapy for the treatment of head and neck cancer patients with minimal residual disease.",
keywords = "Re-labeled MAb E48, radioimmunotherapy, squamous cell carcinoma, xenografts",
author = "Martijn Gerretsen and Visser, {Gerard W M} and Brakenhoff, {Ruud H.} and {van Walsum}, Marijke and Snow, {Gordon B.} and {van Dongen}, {Guus A M S}",
year = "1994",
month = "1",
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doi = "10.1007/BF02789224",
language = "English",
volume = "24-25",
pages = "135--142",
journal = "Cell Biophysics",
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Complete ablation of small squamous cell carcinoma xenografts with186Re-labeled monoclonal antibody E48. / Gerretsen, Martijn; Visser, Gerard W M; Brakenhoff, Ruud H.; van Walsum, Marijke; Snow, Gordon B.; van Dongen, Guus A M S.

In: Cell Biophysics, Vol. 24-25, No. 1-3, 01.01.1994, p. 135-142.

Research output: Contribution to journalArticleAcademicpeer-review

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AU - Gerretsen, Martijn

AU - Visser, Gerard W M

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AB - In previous studies we have shown that in mice bearing head and neck squamous cell carcinoma (HNSCC) xenografts, radioimmunotherapy (RIT) with186Re-labeled MAb E48 resulted in complete regressions in one-third of the tumors (followup >150 d). MAb E48 was labeled with186Re following a novel labeling procedure developed at our institute. The injected dose was 600 μCi, which was the maximum tolerated dose (MTD; <15% wt loss) in these studies. The mean size of the tumors was 140±60 mm3. To investigate whether the therapeutic efficacy of RIT in our xenograft model would be improved when treating smaller xenografts, mice bearing 2 HNSCC xenografts with a vol of 75±17 mm3 (number of mice, n=6; number of tumors, t=12) were treated with 600 μCi of186Re-labeled MAb E48 IgG. All tumors completely regressed and did not regrow during followup (>150 d). In all mice, weight loss did not exceed 10%. to obtain biodistribution data, mice bearing two xenografts with a vol of 58±31 mm3 were injected with 100 μCi of186Re-labeled MAb E48 IgG. The maximum uptake in blood was 26.4% injected dose/g (%ID·g-1) at 2 h pi and was 53.1%ID·g-1 in the tumor at d 7 pi. In normal tissues, no nonspecific accumulation was observed. Based on these biodistribution data, the absorbed cumulative radiation dose was calculated. The accumulated dose in blood and tumor was 2004 cGy and 8580 cGy, respectively. In other tissues, the dose was less than 8.1% of the dose delivered to tumor. These data implicate that RIT with186Re-labeled MAb E48 may be especially suited to be used as adjuvant therapy for the treatment of head and neck cancer patients with minimal residual disease.

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