Preclinical as well as clinical studies with fibroblast interferon (IFN) are still lagging behind on those with leukocyte
interferon. Its side-effects seem to be less pronounced than those of human IFN-α, yet it may be slightly pyrogenic after
intravenous injection. Pyrogenicity of current impure preparations might for the larger part be due to impurities.
Higher doses of HuIFN-β than of HuIFN-α are required to obtain measurable blood titers by intramuscular injections. Since
there is concern about this being due to destruction of the interferon before it has reached its target organ(s), most current
clinical studies use either local (e.g. intratumoral) treatment or intravenous infusions.
A study of topical treatment for acute rhinovirus infection has indicated that there is very little if any chance for fibroblast
interferon to be a clinically useful substance to prevent or cure common cold. In herpetic dendritic keratitis eye drops of
fibroblast interferon may be useful as such or in combination with debridement.
Topical treatment of warts (multiple intralesional injections) has been shown to yield a high success rate, especially in
the case of verrucae vulgares, but less so in the case of verrucae planae juveniles. Studies on condyloma accuminatum are
not so far advanced as to permit a documented conclusion.
Topical (intralesional) treatment of neoplastic diseases has been investigated, especially in Japan, to demonstrate that fibroblast
interferon does have an antineoplastic effectin vivo. While there seems to be little doubt that local delivery does indeed cause tumor nodules to regress, the question is whether
this procedure can offer a true clinical benefit to the patient.
Systemic (intravenous) administration for chronic hepatitis B has been investigated further: given alone or in combination
with adenine-arabinoside, fibroblast interferon seems to be able to reduce the level of viral activity. Whether this will
lead to a generally accepted treatment of chronic active hepatitis is difficult to say at this moment.
In treating herpes zoster in cancer patients, results have been obtained which are comparable to those found for leukocyte
interferon. The practical significance of this finding must be seen in the perspective of recent developments in the chemotherapy
of herpes zoster.
In breast cancer patients given intramuscular injections, metastases in the skin, but not in other organs, showed alterations
suggestive of an effect on tumor progression. Yet there was no true clinical benefit for the patient. In other tumors, e.g.
head and neck epithelioma, no effect was seen.
Intravenous infusions have met with some success in nasopharyngeal carcinoma: temporary stabilization or regression occurred,
but no definitive cures were noted. A large neuroblastoma trial yielded negative results. Disappointing results were also
obtained in non-Hodgkin's lymphoma. In initial studies on myeloma and brain tumors ‘response rates’ of 25% were recorded;
the significance of this in terms of clinical benefit to the patient is not clear yet.