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  1. Article ; Online: A pilot study investigating plasma pharmacokinetics and tolerance of oral capecitabine in carcinoma-bearing dogs.

    Wetzel, Sarah / Fidel, Janean / Whittington, Dale / Villarino, Nicolas F

    BMC veterinary research

    2024  Volume 20, Issue 1, Page(s) 36

    Abstract: Background: Capecitabine is an oral prodrug of the active metabolite 5-fluorouracil, which has been used effectively in human colorectal, head and neck, and mammary carcinomas. Capecitabine has several properties that make it an attractive treatment ... ...

    Abstract Background: Capecitabine is an oral prodrug of the active metabolite 5-fluorouracil, which has been used effectively in human colorectal, head and neck, and mammary carcinomas. Capecitabine has several properties that make it an attractive treatment option for dogs: (i) it is relatively inexpensive, (ii) it has a short half-life in humans, allowing for rapid plasma concentration changes to be achieved with dosage adjustments, (iii) it is effective for treating carcinomas in humans, for which there are no widely-effective oral chemotherapy options in dogs, and (iv) it is thought to preferentially target cancer cells due to different expression of thymidine phosphorylase, thereby decreasing the risk of off-target side effects. However, capecitabine has not been widely explored as a chemotherapy agent for dogs. The goal of this study was to determine the plasma disposition of capecitabine in dogs following a single oral dose and to document any adverse events associated with capecitabine administration over the course of 5 weeks.
    Results: Capecitabine was well tolerated throughout the 5-week study period when administered to 5 dogs with naturally occurring carcinomas at 750 mg/m[Formula: see text] by mouth once daily for 14 consecutive days in a 3-week cycle. No dogs withdrew from the study due to adverse events or other causes. The median AUC[Formula: see text] was 890 h[Formula: see text]ng/ml (range 750-1100 h[Formula: see text]ng/ml); however, the maximum blood concentration and time to reach that concentration of capecitabine was highly variable after a single dose.
    Conclusions: Capecitabine appears well-tolerated as an oral chemotherapy agent for dogs with carcinomas, although individualized dosing may be necessary, and further studies are warranted.
    MeSH term(s) Dogs ; Humans ; Animals ; Capecitabine/therapeutic use ; Pilot Projects ; Deoxycytidine/adverse effects ; Fluorouracil/adverse effects ; Carcinoma/drug therapy ; Carcinoma/veterinary ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Administration, Oral ; Dog Diseases/etiology
    Chemical Substances Capecitabine (6804DJ8Z9U) ; Deoxycytidine (0W860991D6) ; Fluorouracil (U3P01618RT)
    Language English
    Publishing date 2024-01-31
    Publishing country England
    Document type Journal Article
    ZDB-ID 2191675-5
    ISSN 1746-6148 ; 1746-6148
    ISSN (online) 1746-6148
    ISSN 1746-6148
    DOI 10.1186/s12917-023-03805-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Direct Interstitial Treatment of Solid Tumors Using an Injectable Yttrium-90-Polymer Composite.

    Fisher, Darrell R / Fidel, Janean / Maitz, Charles A

    Cancer biotherapy & radiopharmaceuticals

    2019  Volume 35, Issue 1, Page(s) 1–9

    Abstract: Purpose: ...

    Abstract Purpose:
    MeSH term(s) Animals ; Cats ; Disease Models, Animal ; Dogs ; Humans ; Injections ; Neoplasms/drug therapy ; Radiotherapy Dosage ; Yttrium Radioisotopes/pharmacology ; Yttrium Radioisotopes/therapeutic use
    Chemical Substances Yttrium Radioisotopes ; Yttrium-90 (1K8M7UR6O1)
    Language English
    Publishing date 2019-10-17
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1315649-4
    ISSN 1557-8852 ; 1084-9785
    ISSN (online) 1557-8852
    ISSN 1084-9785
    DOI 10.1089/cbr.2019.2947
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: TOLERABILITY AND TUMOR RESPONSE OF A NOVEL LOW-DOSE PALLIATIVE RADIATION THERAPY PROTOCOL IN DOGS WITH TRANSITIONAL CELL CARCINOMA OF THE BLADDER AND URETHRA.

    Choy, Kevin / Fidel, Janean

    Veterinary radiology & ultrasound : the official journal of the American College of Veterinary Radiology and the International Veterinary Radiology Association

    2016  Volume 57, Issue 3, Page(s) 341–351

    Abstract: Previously reported radiation protocols for transitional cell carcinoma of the canine lower urinary tract have been ineffective or associated with increased side effects. Objectives of this retrospective, cross-sectional study were to describe safety of ... ...

    Abstract Previously reported radiation protocols for transitional cell carcinoma of the canine lower urinary tract have been ineffective or associated with increased side effects. Objectives of this retrospective, cross-sectional study were to describe safety of and tumor responses for a novel palliative radiation protocol for transitional cell carcinoma in dogs. Included dogs had cytologically or histologically confirmed transitional cell carcinoma of the bladder or urethra, and were treated with 10 once-daily fractions (Monday-Friday) of 2.7 Gy. Thirteen dogs were sampled, with six treated using radiation as first-line (induction) therapy and seven treated using radiation as rescue therapy after failing previous chemotherapy. Within 6 weeks of radiation, 7.6% (1/13) dogs had a complete response, 53.8% (7/13) partial response, 38.5% (5/13) stable disease, and none had progressive disease. Three patients presenting with urethral obstruction had spontaneous micturition restored during the treatment protocol. A single patient with unilateral ureteral obstruction was patent at recheck examination. Median survival time from time of initial diagnosis was 179 days. Median survival time from start of radiation was 150 days. Acute radiation side effects occurred in 31% (4/13) patients and were classified as grade 1 or 2. No significant late side radiation side effects were reported. No variables examined were identified as prognostic factors. Findings indicated that the reported radiation protocol was safe in this sample of dogs with bladder and urethral transitional cell carcinoma. Future prospective studies are needed to determine utility of this treatment as a rescue therapy in patients with complete urinary tract obstruction.
    MeSH term(s) Animals ; Carcinoma, Transitional Cell/radiotherapy ; Carcinoma, Transitional Cell/veterinary ; Dog Diseases/radiotherapy ; Dogs ; Palliative Care ; Survival ; Urethra/pathology ; Urinary Bladder/pathology ; Urogenital Neoplasms/radiotherapy ; Urogenital Neoplasms/veterinary
    Language English
    Publishing date 2016-05
    Publishing country England
    Document type Journal Article
    ZDB-ID 2142058-0
    ISSN 1740-8261 ; 1058-8183
    ISSN (online) 1740-8261
    ISSN 1058-8183
    DOI 10.1111/vru.12339
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Radiation therapy in horses.

    Fidel, Janean L

    Compendium (Yardley, PA)

    2010  Volume 32, Issue 4, Page(s) E3

    Abstract: Although the diagnosis of cancer is relatively uncommon in horses, tumors do occur in this species. Surgery, radiation, and chemotherapy are traditional cancer treatments in all species. In equine patients, surgery has often been the only treatment ... ...

    Abstract Although the diagnosis of cancer is relatively uncommon in horses, tumors do occur in this species. Surgery, radiation, and chemotherapy are traditional cancer treatments in all species. In equine patients, surgery has often been the only treatment offered; however, not all tumors can be controlled with surgery alone. In small animal oncology, newer and better therapies are in demand and available. Radiation therapy is often used to control or palliate tumors locally, especially to satisfy clients who demand sophisticated treatments. The large size of equine patients can make radiation therapy difficult, but it is a valuable tool for treating cancer and should not be overlooked when treating horses.
    MeSH term(s) Animals ; Combined Modality Therapy ; Dose-Response Relationship, Radiation ; Horse Diseases/radiotherapy ; Horse Diseases/surgery ; Horses ; Neoplasms/radiotherapy ; Neoplasms/surgery ; Neoplasms/veterinary
    Language English
    Publishing date 2010-04
    Publishing country United States
    Document type Journal Article ; Review
    ISSN 1940-8315
    ISSN (online) 1940-8315
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Comparative whole transcriptome analysis of gene expression in three canine soft tissue sarcoma types.

    Lam, Lydia / Tien, Tien / Wildung, Mark / White, Laura / Sellon, Rance K / Fidel, Janean L / Shelden, Eric A

    PloS one

    2022  Volume 17, Issue 9, Page(s) e0273705

    Abstract: Soft tissue sarcomas are pleiotropic tumors of mesenchymal cell origin. These tumors are rare in humans but common in veterinary practice, where they comprise up to 15% of canine skin and subcutaneous cancers. Because they present similar morphologies, ... ...

    Abstract Soft tissue sarcomas are pleiotropic tumors of mesenchymal cell origin. These tumors are rare in humans but common in veterinary practice, where they comprise up to 15% of canine skin and subcutaneous cancers. Because they present similar morphologies, primary sites, and growth characteristics, they are treated similarly, generally by surgical resection followed by radiation therapy. Previous studies have examined a variety of genetic changes as potential drivers of tumorigenesis and progression in soft tissue sarcomas as well as their use as markers for soft tissue sarcoma subtypes. However, few studies employing next generation sequencing approaches have been published. Here, we have examined gene expression patterns in canine soft tissue sarcomas using RNA-seq analysis of samples obtained from archived formalin-fixed and paraffin-embedded tumors. We provide a computational framework for using resulting data to categorize tumors, perform cross species comparisons and identify genetic changes associated with tumorigenesis. Functional overrepresentation analysis of differentially expressed genes further implicate both common and tumor-type specific transcription factors as potential mediators of tumorigenesis and aggression. Implications for tumor-type specific therapies are discussed. Our results illustrate the potential utility of this approach for the discovery of new therapeutic approaches to the management of canine soft tissue sarcomas and support the view that both common and tumor-type specific mechanisms drive the development of these tumors.
    MeSH term(s) Animals ; Carcinogenesis ; Cell Transformation, Neoplastic ; Dogs ; Gene Expression Profiling ; Humans ; Sarcoma/genetics ; Sarcoma/pathology ; Sarcoma/veterinary ; Soft Tissue Neoplasms/genetics ; Soft Tissue Neoplasms/pathology ; Soft Tissue Neoplasms/veterinary ; Transcriptome
    Language English
    Publishing date 2022-09-13
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2267670-3
    ISSN 1932-6203 ; 1932-6203
    ISSN (online) 1932-6203
    ISSN 1932-6203
    DOI 10.1371/journal.pone.0273705
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Metronomic administration of lomustine following palliative radiation therapy for appendicular osteosarcoma in dogs.

    Duffy, Megan E / Anderson, Christie L / Choy, Kevin / Fidel, Janean L

    The Canadian veterinary journal = La revue veterinaire canadienne

    2018  Volume 59, Issue 2, Page(s) 136–142

    Abstract: The purpose of this study was to determine if metronomic administration of lomustine following palliative radiation therapy (RT) improved length of palliation and therefore survival in dogs with appendicular osteosarcoma compared to treatment with ... ...

    Abstract The purpose of this study was to determine if metronomic administration of lomustine following palliative radiation therapy (RT) improved length of palliation and therefore survival in dogs with appendicular osteosarcoma compared to treatment with palliative radiation alone. A search of medical records identified dogs with appendicular osteosarcoma, treated with palliative RT (2 fractions of 8 Gray in a 24 hour time frame, day 0 and day 1; or day 0, 6 hours apart). Data collected included signalment, history, clinical signs, physical examination findings, clinicopathologic abnormalities, extent of disease, response, toxicity, other therapy, survival time, and whether dogs received metronomic lomustine (ML) or not. Of 86 patients, 43 received ML while 43 did not. Median survival time (MST) was not significantly different (
    MeSH term(s) Animals ; Antineoplastic Agents/administration & dosage ; Antineoplastic Agents/therapeutic use ; Bone Neoplasms/drug therapy ; Bone Neoplasms/radiotherapy ; Bone Neoplasms/veterinary ; Dog Diseases/drug therapy ; Dogs ; Extremities ; Female ; Lomustine/administration & dosage ; Lomustine/therapeutic use ; Male ; Osteosarcoma/drug therapy ; Osteosarcoma/radiotherapy ; Osteosarcoma/veterinary ; Palliative Care ; Radiotherapy/veterinary ; Retrospective Studies
    Chemical Substances Antineoplastic Agents ; Lomustine (7BRF0Z81KG)
    Language English
    Publishing date 2018-01-31
    Publishing country Canada
    Document type Journal Article
    ZDB-ID 41603-4
    ISSN 0008-5286
    ISSN 0008-5286
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Development of prednisone resistance in naïve canine lymphoma: Longitudinal evaluation of NR3C1α, ABCB1, and 11β‐HSD mRNA expression

    Hanot, Camille C / Mealey, Katrina L / Fidel, Janean L / Burke, Neal S / White, Laura A / Sellon, Rance K

    Journal of veterinary pharmacology and therapeutics. 2020 Mar., v. 43, no. 2

    2020  

    Abstract: Prednisone resistance develops rapidly and essentially universally when dogs with lymphoma are treated with corticosteroids. We investigated naturally occurring mechanisms of prednisone resistance in seven dogs with naïve multicentric lymphoma, treated ... ...

    Abstract Prednisone resistance develops rapidly and essentially universally when dogs with lymphoma are treated with corticosteroids. We investigated naturally occurring mechanisms of prednisone resistance in seven dogs with naïve multicentric lymphoma, treated with oral prednisone; four dogs were administered concurrent cytotoxic chemotherapy. Expression of NR3C1α, ABCB1 (formerly MDR1), 11β‐HSD1, and 11β‐HSD2 mRNA was evaluated in neoplastic lymph nodes by real‐time RT‐PCR. Changes of expression levels at diagnosis and at time of clinical resistance to prednisone were compared longitudinally using a Wilcoxon signed‐rank test. Clinical resistance to prednisone was observed after a median of 68 days (range: 7–348 days) after initiation of treatment. Relative to pretreatment samples, prednisone resistance was associated with decreased NR3C1α expression in biopsies of all dogs with high‐grade lymphoma (six dogs, p=.031); one dog with indolent T‐zone lymphoma had increased expression of NR3C1α. Resistance was not consistently associated with changes in ABCB1, 11β‐HSD1, or 11β‐HSD2 expression. Decreased expression of the glucocorticoid receptor (NR3C1α) may play a role in conferring resistance to prednisone in dogs with lymphoma. Results do not indicate a broad role for changes in expression of ABCB1, 11β‐HSD1, and 11β‐HSD2 in the emergence of prednisone resistance in lymphoma‐bearing dogs.
    Keywords adrenal cortex hormones ; biopsy ; cytotoxicity ; dogs ; drug therapy ; gene expression ; glucocorticoid receptors ; lymph nodes ; lymphoma ; messenger RNA ; prednisone ; quantitative polymerase chain reaction ; reverse transcriptase polymerase chain reaction
    Language English
    Dates of publication 2020-03
    Size p. 231-236.
    Publishing place John Wiley & Sons, Ltd
    Document type Article
    Note JOURNAL ARTICLE
    ZDB-ID 435216-6
    ISSN 1365-2885 ; 0140-7783
    ISSN (online) 1365-2885
    ISSN 0140-7783
    DOI 10.1111/jvp.12837
    Database NAL-Catalogue (AGRICOLA)

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  8. Article: A prospective, multi‐centre, Veterinary Radiation Therapy Oncology Group study reveals potential efficacy of toceranib phosphate (Palladia) as a primary or adjuvant agent in the treatment of canine nasal carcinoma

    Ehling, Tara Jean / Klein, Mary Kay / Smith, Lauren / Prescott, Deborah / Haney, Siobhan / Looper, Jayme / LaDue, Tracey / Brawner, William / Fidel, Janean / Shiomitsu, Keijiro / Green, Eric / Saba, Corey / Turek, Michelle / Farrelly, John

    Veterinary and comparative oncology. 2022 Mar., v. 20, no. 1

    2022  

    Abstract: Radiation is the standard of care for dogs with nasal tumours. The addition of another therapy that could improve outcome without increasing toxicity is attractive. Medical therapy that could offer better outcome than maximally tolerated dose ... ...

    Abstract Radiation is the standard of care for dogs with nasal tumours. The addition of another therapy that could improve outcome without increasing toxicity is attractive. Medical therapy that could offer better outcome than maximally tolerated dose chemotherapy when radiation therapy (RT) is not possible or is declined is also attractive. This article reports the findings from a prospective, multi‐centre, non‐randomized, Veterinary Radiation Therapy Oncology Group clinical trial designed to evaluate whether toceranib phosphate (toceranib) has primary activity and if the addition of toceranib to RT could positively impact outcome. Owner's discretion determined enrolment in toceranib alone or toceranib + RT arm. Historical controls for radiation alone were selected from patients treated with identical RT and imaging protocols. Responses were evaluated with pre‐treatment and week‐16 CT scans. RT total dose of 42 Gy was completed in 10 fractions. Sixty‐three dogs enrolled from 10 study sites. Overall response rates (CR + PR) were significantly improved in the toceranib + RT (79.4%) and RT alone (68.9%) arms over toceranib alone (22%) (p = .011). Clinical benefit rates (CR + PR + SD) were significantly improved in the toceranib + RT arm over the RT alone arm at 97.3% and 79.2% respectively (p = .036). Treatment with toceranib alone, toceranib + RT and RT alone resulted in median survival times of 298, 615 and 368 days respectively, but were not statistically significantly different (p = .0502). Adverse events associated with toceranib administration did not potentiate the RT side effect profile. Toceranib appears to have primary activity against nasal carcinoma.
    Keywords adjuvants ; adverse effects ; carcinoma ; clinical trials ; dogs ; drug therapy ; maximum tolerated dose ; nose ; phosphates ; radiotherapy ; toxicity
    Language English
    Dates of publication 2022-03
    Size p. 293-303.
    Publishing place Blackwell Publishing Ltd
    Document type Article
    Note JOURNAL ARTICLE
    ZDB-ID 2129634-0
    ISSN 1476-5829 ; 1476-5810
    ISSN (online) 1476-5829
    ISSN 1476-5810
    DOI 10.1111/vco.12776
    Database NAL-Catalogue (AGRICOLA)

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  9. Article ; Online: Development of prednisone resistance in naïve canine lymphoma: Longitudinal evaluation of NR3C1α, ABCB1, and 11β-HSD mRNA expression.

    Hanot, Camille C / Mealey, Katrina L / Fidel, Janean L / Burke, Neal S / White, Laura A / Sellon, Rance K

    Journal of veterinary pharmacology and therapeutics

    2020  Volume 43, Issue 2, Page(s) 231–236

    Abstract: Prednisone resistance develops rapidly and essentially universally when dogs with lymphoma are treated with corticosteroids. We investigated naturally occurring mechanisms of prednisone resistance in seven dogs with naïve multicentric lymphoma, treated ... ...

    Abstract Prednisone resistance develops rapidly and essentially universally when dogs with lymphoma are treated with corticosteroids. We investigated naturally occurring mechanisms of prednisone resistance in seven dogs with naïve multicentric lymphoma, treated with oral prednisone; four dogs were administered concurrent cytotoxic chemotherapy. Expression of NR3C1α, ABCB1 (formerly MDR1), 11β-HSD1, and 11β-HSD2 mRNA was evaluated in neoplastic lymph nodes by real-time RT-PCR. Changes of expression levels at diagnosis and at time of clinical resistance to prednisone were compared longitudinally using a Wilcoxon signed-rank test. Clinical resistance to prednisone was observed after a median of 68 days (range: 7-348 days) after initiation of treatment. Relative to pretreatment samples, prednisone resistance was associated with decreased NR3C1α expression in biopsies of all dogs with high-grade lymphoma (six dogs, p=.031); one dog with indolent T-zone lymphoma had increased expression of NR3C1α. Resistance was not consistently associated with changes in ABCB1, 11β-HSD1, or 11β-HSD2 expression. Decreased expression of the glucocorticoid receptor (NR3C1α) may play a role in conferring resistance to prednisone in dogs with lymphoma. Results do not indicate a broad role for changes in expression of ABCB1, 11β-HSD1, and 11β-HSD2 in the emergence of prednisone resistance in lymphoma-bearing dogs.
    MeSH term(s) 11-beta-Hydroxysteroid Dehydrogenase Type 1/genetics ; 11-beta-Hydroxysteroid Dehydrogenase Type 1/metabolism ; 11-beta-Hydroxysteroid Dehydrogenase Type 2/genetics ; 11-beta-Hydroxysteroid Dehydrogenase Type 2/metabolism ; ATP Binding Cassette Transporter, Subfamily B, Member 1/genetics ; ATP Binding Cassette Transporter, Subfamily B, Member 1/metabolism ; Animals ; Antineoplastic Agents, Hormonal/administration & dosage ; Antineoplastic Agents, Hormonal/therapeutic use ; Cohort Studies ; Dog Diseases/drug therapy ; Dogs ; Drug Administration Schedule ; Drug Resistance, Neoplasm/genetics ; Female ; Gene Expression Regulation/drug effects ; Lymphoma/drug therapy ; Lymphoma/veterinary ; Male ; Prednisone/administration & dosage ; Prednisone/therapeutic use ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Receptors, Glucocorticoid/genetics ; Receptors, Glucocorticoid/metabolism
    Chemical Substances ATP Binding Cassette Transporter, Subfamily B, Member 1 ; Antineoplastic Agents, Hormonal ; RNA, Messenger ; Receptors, Glucocorticoid ; 11-beta-Hydroxysteroid Dehydrogenase Type 1 (EC 1.1.1.146) ; 11-beta-Hydroxysteroid Dehydrogenase Type 2 (EC 1.1.1.146) ; Prednisone (VB0R961HZT)
    Language English
    Publishing date 2020-01-14
    Publishing country England
    Document type Journal Article
    ZDB-ID 435216-6
    ISSN 1365-2885 ; 0140-7783
    ISSN (online) 1365-2885
    ISSN 0140-7783
    DOI 10.1111/jvp.12837
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: A prospective, multi-centre, Veterinary Radiation Therapy Oncology Group study reveals potential efficacy of toceranib phosphate (Palladia) as a primary or adjuvant agent in the treatment of canine nasal carcinoma.

    Ehling, Tara Jean / Klein, Mary Kay / Smith, Lauren / Prescott, Deborah / Haney, Siobhan / Looper, Jayme / LaDue, Tracey / Brawner, William / Fidel, Janean / Shiomitsu, Keijiro / Green, Eric / Saba, Corey / Turek, Michelle / Farrelly, John

    Veterinary and comparative oncology

    2021  Volume 20, Issue 1, Page(s) 293–303

    Abstract: Radiation is the standard of care for dogs with nasal tumours. The addition of another therapy that could improve outcome without increasing toxicity is attractive. Medical therapy that could offer better outcome than maximally tolerated dose ... ...

    Abstract Radiation is the standard of care for dogs with nasal tumours. The addition of another therapy that could improve outcome without increasing toxicity is attractive. Medical therapy that could offer better outcome than maximally tolerated dose chemotherapy when radiation therapy (RT) is not possible or is declined is also attractive. This article reports the findings from a prospective, multi-centre, non-randomized, Veterinary Radiation Therapy Oncology Group clinical trial designed to evaluate whether toceranib phosphate (toceranib) has primary activity and if the addition of toceranib to RT could positively impact outcome. Owner's discretion determined enrolment in toceranib alone or toceranib + RT arm. Historical controls for radiation alone were selected from patients treated with identical RT and imaging protocols. Responses were evaluated with pre-treatment and week-16 CT scans. RT total dose of 42 Gy was completed in 10 fractions. Sixty-three dogs enrolled from 10 study sites. Overall response rates (CR + PR) were significantly improved in the toceranib + RT (79.4%) and RT alone (68.9%) arms over toceranib alone (22%) (p = .011). Clinical benefit rates (CR + PR + SD) were significantly improved in the toceranib + RT arm over the RT alone arm at 97.3% and 79.2% respectively (p = .036). Treatment with toceranib alone, toceranib + RT and RT alone resulted in median survival times of 298, 615 and 368 days respectively, but were not statistically significantly different (p = .0502). Adverse events associated with toceranib administration did not potentiate the RT side effect profile. Toceranib appears to have primary activity against nasal carcinoma.
    MeSH term(s) Animals ; Antineoplastic Agents/therapeutic use ; Carcinoma/veterinary ; Dog Diseases/drug therapy ; Dog Diseases/radiotherapy ; Dogs ; Indoles ; Nose Neoplasms/drug therapy ; Nose Neoplasms/radiotherapy ; Nose Neoplasms/veterinary ; Prospective Studies ; Pyrroles/therapeutic use
    Chemical Substances Antineoplastic Agents ; Indoles ; Pyrroles ; toceranib phosphate (24F9PF7J3R)
    Language English
    Publishing date 2021-10-26
    Publishing country England
    Document type Journal Article
    ZDB-ID 2129634-0
    ISSN 1476-5829 ; 1476-5810
    ISSN (online) 1476-5829
    ISSN 1476-5810
    DOI 10.1111/vco.12776
    Database MEDical Literature Analysis and Retrieval System OnLINE

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