CRM197 and cancer: effects of intratumoral administration. Issue 1 (1st September 2004)
- Record Type:
- Journal Article
- Title:
- CRM197 and cancer: effects of intratumoral administration. Issue 1 (1st September 2004)
- Main Title:
- CRM197 and cancer: effects of intratumoral administration
- Authors:
- Buzzi, Silvio
Rubboli, Diego
Buzzi, Giorgio
Buzzi, Anna Maria
Morisi, Claudio
Pironi, Flavio - Abstract:
- Background: Cross-reacting material 197 is a nontoxic mutant of diphtheria toxin that cross-reacts immunologically with the native counterpart. The molecule was recently tested as a systemic anticancer agent with promising results but its exact mechanism of action has remained unclear. Objective: The main goal of this study was to investigate this mechanism through the possible histologic changes induced by direct inoculation of the molecule into a tumor lesion. A secondary objective was to evaluate toxic, hematologic and antitumor effects of the procedure. Methods: Cross-reacting material 197 was administered by injection into accessible lesions of 12 patients with advanced cancer refractory to standard therapies. Two different doses were used according to the maximal diameter of the selected lesions. Lesions up to 2.5 cm were injected with 0.017 mg/day contained in 0.33 ml of a dilution buffer. Lesions up to 5.0 cm were injected with 0.051 mg/day contained in 1.0 ml of dilution buffer. The treatment schedule consisted of six injections administered on alternate days. A biopsy was taken from each selected lesion before the start of treatment and again 15 days later. Results: Toxicities and effects of cross-reacting material 197 on the injected lesion varied according to the patients'' degree of reactivity to diphtheria toxin. Patients with poor reactivity experienced negligible toxicity and no change or minimal change in the number of circulating neutrophils, in theBackground: Cross-reacting material 197 is a nontoxic mutant of diphtheria toxin that cross-reacts immunologically with the native counterpart. The molecule was recently tested as a systemic anticancer agent with promising results but its exact mechanism of action has remained unclear. Objective: The main goal of this study was to investigate this mechanism through the possible histologic changes induced by direct inoculation of the molecule into a tumor lesion. A secondary objective was to evaluate toxic, hematologic and antitumor effects of the procedure. Methods: Cross-reacting material 197 was administered by injection into accessible lesions of 12 patients with advanced cancer refractory to standard therapies. Two different doses were used according to the maximal diameter of the selected lesions. Lesions up to 2.5 cm were injected with 0.017 mg/day contained in 0.33 ml of a dilution buffer. Lesions up to 5.0 cm were injected with 0.051 mg/day contained in 1.0 ml of dilution buffer. The treatment schedule consisted of six injections administered on alternate days. A biopsy was taken from each selected lesion before the start of treatment and again 15 days later. Results: Toxicities and effects of cross-reacting material 197 on the injected lesion varied according to the patients'' degree of reactivity to diphtheria toxin. Patients with poor reactivity experienced negligible toxicity and no change or minimal change in the number of circulating neutrophils, in the post-treatment histology of their lesions and in the final lesion size. Patients with strong reactivity experienced mild-to-moderate flu-like syndrome, a prominent increase in the number of circulating neutrophils and a dense neutrophilic infiltration of the injected lesion leading to inflammation and, sometimes, to suppuration. Shrinkage of the index lesion ranging from 60 to 100% was observed in three of the patients. Conclusion: Neutrophils seemed to play a crucial role in achieving these results. One patient was available for post-treatment biopsy only at day 30 from the start of treatment. Examination of these specimens evidenced a striking granulomatous reaction surrounding a core of dead and viable tumor cells. … (more)
- Is Part Of:
- Therapy. Volume 1:Issue 1(2004)
- Journal:
- Therapy
- Issue:
- Volume 1:Issue 1(2004)
- Issue Display:
- Volume 1, Issue 1 (2004)
- Year:
- 2004
- Volume:
- 1
- Issue:
- 1
- Issue Sort Value:
- 2004-0001-0001-0000
- Page Start:
- 61
- Page End:
- 66
- Publication Date:
- 2004-09-01
- Subjects:
- cancer -- clinical trial -- immunological antitumor effect -- intratumoral administration -- neutrophils -- nontoxic diphtheria toxin
Therapeutics -- Periodicals
Chemotherapy -- Periodicals
615.505 - Journal URLs:
- http://www.futuremedicine.com/loi/cpr ↗
http://www.futuremedicine.com/ ↗ - DOI:
- 10.2217/14750708.1.1.61 ↗
- Languages:
- English
- ISSNs:
- 1475-0708
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8814.766000
British Library DSC - BLDSS-3PM
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- 16483.xml