AI Article Synopsis

  • The acute rat T-cell leukaemia (Roser) spreads to the epididymal and testicular interstitial tissues during its progression, while the gonadal duct system remains unaffected.
  • There is evidence of meningeal invasion during routine passage which was not observed in earlier studies, and leukemia relapses can happen up to 80 days post initial treatment with carmustine even after periods of remission.
  • Two doses of carmustine can effectively eradicate the leukaemia, particularly if timed appropriately after the introduction of cancer cells, and female subjects are more responsive to treatment than males, suggesting the importance of the gonadal environment in disease progression.

Article Abstract

During the haematogenous dissemination of this acute rat T-cell (Roser) leukaemia, infiltration of both epididymal and testicular interstitial tissue has now been demonstrated, probably as an invariable occurrence. The gonadal duct system itself was not invaded. In contrast to an earlier histopathological study with this leukaemia, meningeal invasion has also been encountered during routine passage. Furthermore, subsequent to remissions induced by carmustine (BCNU), relapse could occur as long as 80 days after the 20 day end point in control animals. This was associated with extensive infiltration of the meninges as well as in the male gonadal interstitium, the proximal epididymis being particularly vulnerable. Two doses of carmustine at intervals of one week could eradicate the disease even during the phase of logarithmic growth of the leukaemic cells, this result depending upon the level of treatment and time of dosing post-inoculation with leukaemic cells. Females carrying the disease were shown to be more readily cured than males, probably related to entry of leukaemia cells into the gonadal interstitium. This T-cell leukaemia appears to be an excellent model for the study and prospective chemotherapy of testicular relapse in acute lymphoblastic leukaemia.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976988PMC
http://dx.doi.org/10.1038/bjc.1984.228DOI Listing

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