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S MacCallum

Publications and source records attributed to S MacCallum.

4 recordsLinked to original sources

Role of alpha interferon in multiple myeloma.

Interferons are soluble proteins produced by cells in response to viruses. Although they were first introduced as therapeutic agents for myeloma in 1979 their exact role in the management of myeloma remains to be precisely defined. Interferons have both anti-proliferative and immune regulation effects, but the predominant mode of action of interferons in myeloma is still unclear. Recombinant alpha interferon has been used in clinical trials as a single induction agent, co-induction agents with combination chemotherapy, as salvage therapy, and as therapy to maintain plateau phase after conventional chemotherapy or complete remission after auto or allogeneic transplantation. Interferon as a single induction or co-induction agent with other forms of chemotherapy appears to be of only minimal benefit in myeloma. However, its role as maintenance agent has received a great deal of interest and investigation. Its most beneficial role would appear to be in those patients who have had good responses to either conventional therapy or to bone marrow transplantation and the beneficial role of interferon in the maintenance of plateau phase is gaining credence. Its maximum advantage appears to be in patients with initial good response who have obtained plateau phase, or in patients who have developed complete remission after auto transplantation. It also has a role as salvage treatment in refractory patients with myeloma where the combination of interferon and dexamethazone may be a useful therapeutic modality.

Antineoplastic Agents↗

Variability on serial testing of pattern reversal visual evoked potential latencies from full-field, half-field and foveal stimulation in control subjects.

The change in pattern reversal visual evoked potential (PRVEP) latency over time (test-retest variability, TRV) was assessed in 30 (16 males, 14 females) adult control subjects using full-field (FF), half-field (HF) and foveal (central-field, CF) stimulation. The mean test-retest interval (TRI) was 20.5 months with a range of 18-21.5 months. There were no significant test-retest latency differences in either sex and furthermore there were no significant inter-sex differences in any of the test-retest parameters. Because of the latter finding the test-retest upper limit of normal for each parameter as defined by the mean value + 2.5 S.D. was taken as the largest value obtained in either sex. Thus the test-retest upper limits of normal for absolute latency from FF, right HF, left HF and CF stimulation were 6, 7, 9 and 7 msec, respectively; for interocular latency differences (ILD) from FF and CF stimulation were 4 and 5 msec respectively; and for right HF to left HF intraocular latency difference (IOLD) was 7 msec. It is concluded that the TRV was sufficiently small in our control group with each of the stimulus techniques to make all of them potentially useful in serial PRVEP studies. Furthermore the extra information provided by CF and HF stimulation may increase the sensitivity and accuracy with which change can be monitored.

Adult↗