Recombinant interferon alfa-2a in metastatic renal cell carcinoma: assessment of antitumor activity and anti-interferon antibody formation.
- 1 October 1988
- journal article
- research article
- Published by American Society of Clinical Oncology (ASCO) in Journal of Clinical Oncology
- Vol. 6 (10) , 1604-1610
- https://doi.org/10.1200/jco.1988.6.10.1604
Abstract
Twenty-one patients with advanced, measurable, renal cell carcinoma (RCC) were administered recombinant interferon alfa-2a (rIFN-alpha 2a) (Roferon-A; Roche Laboratories, Nutley, NJ) intramuscularly beginning at 3 x 10(6) units and escalating to 36 x 10(6) units, 5 d/wk for a total induction period of 14 weeks. rIFN-alpha 2a antibody production was measured using an enzyme immunoassay (EIA). Those sera found to be positive for presence of antibody by the EIA were tested for the presence of neutralizing antibodies (NA) by an antiviral neutralization bioassay (ANB). All patients were evaluable for toxicity, and 19 were evaluable for response and for incidence of antibody formation. Five patients (26%; 95% confidence interval, 6% to 46%) had complete responses (CR) or partial responses (PR) with a median duration of 283 days. An additional ten patients (53%) had minor tumor regressions with a median duration of 86 days. Fifty-one percent of evaluable patients are alive at 18.6 months. Antibodies to rIFN-alpha 2a as measured by the EIA, were detected in 12 (63%) patients. NA were measured in the serum of six (50%) of those EIA-positive patients. Overall, six of 19 patients (32%) developed NA. Median time to the development of antibody as measured by EIA or NA was 8 and 14 weeks, respectively. Median NA titer was 1,200 IFN neutralizing U/mL. NA-positive and -negative patients had a median duration of response of 13.7 v 9.9 months, and survival of greater than 21.3 v 18.3 months, respectively. Clinical toxicity was mild and not therapeutically limiting. Autoantibody production (ANA, rheumatoid factor [RF], Coombs' direct/indirect) occurred in both NA-positive and -negative patients. The clinical significance of the antibodies to rIFN-alpha 2a and the associated autoantibody formation remain unclear; however, presence of antibody was not associated with adverse clinical sequelae.This publication has 19 references indexed in Scilit:
- A RANDOMIZED STUDY OF LOW AND HIGH-DOSES OF LEUKOCYTE ALPHA-INTERFERON IN METASTATIC RENAL-CELL CARCINOMA - THE AMERICAN-CANCER-SOCIETY COLLABORATIVE TRIAL1985
- Phase II study of recombinant leukocyte a interferon (rIFN-αA) in disseminated malignant melanomaCancer, 1984
- Treatment of Advanced Non-Hodgkin's Lymphoma with Recombinant Leukocyte a InterferonNew England Journal of Medicine, 1984
- Phase II study of low-dose recombinant leukocyte A interferon in disseminated malignant melanoma.Journal of Clinical Oncology, 1984
- Collaborative phase I-II study of recombinant DNA-produced leukocyte interferon (clone A) in metastatic breast cancer, malignant lymphoma, and multiple myelomaThe American Journal of Medicine, 1984
- Synergistic antiviral and antiproliferative activities of Escherichia coli-derived human alpha, beta, and gamma interferonsJournal of Virology, 1984
- POSITIVE INTERACTIONS BETWEEN HUMAN INTERFERON AND CYCLOPHOSPHAMIDE OR ADRIAMYCIN IN A HUMAN-TUMOR MODEL SYSTEM1984
- ENHANCED EXPRESSION OF SURFACE TUMOR-ASSOCIATED ANTIGENS ON HUMAN-BREAST AND COLON-TUMOR CELLS AFTER RECOMBINANT HUMAN-LEUKOCYTE ALPHA-INTERFERON TREATMENT1984
- Human tumor necrosis factor produced by human B-cell lines: synergistic cytotoxic interaction with human interferon.Proceedings of the National Academy of Sciences, 1983
- ANTIBODIES TO HUMAN LEUCOCYTE INTERFERONS IN CANCER PATIENTSThe Lancet, 1983