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[Interleukin 2 based ambulatory therapy of metastatic renal cell carcinoma].

AbstractBACKGROUND:
In metastatic renal cell carcinoma, strictly immunomodulatory maneuvers using systemic interleukin-2 have produced objective tumor remissions and led to an effective palliation. The goals of an improved cost effectiveness and therapeutic index of interleukin-2 require the design of risk factor adapted individual therapeutic strategies for the outpatient setting.
PATIENTS AND METHODS:
In 215 consecutive single institution patients with advanced metastatic renal cell carcinoma, the efficacy and tolerance of different subcutaneous recombinant interleukin-2 (rIL-2) based home therapies was assessed. Independent risk factors at pre-treatment level were identified and patient survival was compared between risk groups and therapies. Treatment consisted of s.c. rIL-2 alone and s.c. rIL-2 in combination with recombinant interferon-alpha 2 (rIFN-alpha 2), with or without intravenous 5-fluorouracil (5-FU).
RESULTS:
Overall objective response rate in 215 patients was 33% (95% confidence interval, 26 to 39%). Among patients receiving rIL-2 alone (n = 16), there was 1 partial remission (overall response, 6%). In patients on rIL-2 and rIFN-alpha 2 in combination (n = 79), 6 complete and 16 partial remissions occurred (overall response, 28%). Of 120 patients receiving a combination of rIL-2, rIFN-alpha 2 and 5-FU, 13 patients achieved a complete and 34 a partial remission (lung, liver, local relapse, bone, adrenal, pleural, and thyroid metastases; overall response 39%). Duration of complete and partial remissions ranged from 10 to 55+ months, and 3 to 32 months, respectively, in rIL-2/rIFN-alpha 2 treated patients, and from 8+ to 47+ months and from 3 to 31+ months, respectively, in rIL-2/rIFN-alpha/5-FU treated patients. Of all patients 5% achieved long-lasting remissions and remain disease-free. In the majority of patients, systemic toxicity of s.c. rIL-2 based protocols was limited to grade 1 or 2 constitutional symptoms i.e., fever, chills, malaise, and anorexia; this allowed for an outpatient therapy. No life-threatening toxicity and no toxic deaths occurred.
CONCLUSIONS:
The present outpatient rIL-2 triple drug combination protocol was as effective as the most aggressive i.v. rIL-2 regimen available; it substantially improved the therapeutic index and cost effectiveness of rIL-2 therapy in metastatic renal cell carcinoma stratified for risk.
AuthorsJ Atzpodien, H Kirchner, H Poliwoda
JournalMedizinische Klinik (Munich, Germany : 1983) (Med Klin (Munich)) Vol. 91 Suppl 3 Pg. 38-43 (Apr 12 1996) ISSN: 0723-5003 [Print] Germany
Vernacular TitleInterleukin-2-haltige ambulante Therapie des metastasierenden Nierenzellkarzinoms.
PMID8692118 (Publication Type: Clinical Trial, Controlled Clinical Trial, English Abstract, Journal Article)
Chemical References
  • Interleukin-2
  • Recombinant Proteins
Topics
  • Adult
  • Aged
  • Ambulatory Care
  • Carcinoma, Renal Cell (mortality, pathology, therapy)
  • Female
  • Follow-Up Studies
  • Humans
  • Interleukin-2 (administration & dosage, adverse effects)
  • Kidney Neoplasms (mortality, pathology, therapy)
  • Male
  • Middle Aged
  • Neoplasm Metastasis
  • Neoplasm Staging
  • Palliative Care
  • Recombinant Proteins (administration & dosage, adverse effects)
  • Survival Rate

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