Adjuvant Immunotherapy Provides No Clinical Benefit in Patients
with High‑risk Renal Cell Carcinoma
For renal cell carcinoma
patients at high risk of relapse following nephrectomy, adjuvant
therapy with the combination of interleukin-2 (Proleukin),
interferon alfa, and fluorouracil (5-FU) provides no survival
benefit over observation alone, according to a phase III trial
conducted by the European Organisation for Research and Treatment
of Cancer (EORTC). Michael Aitchison, MD, of the Beatson Oncology
Centre in Glasgow, presented the final results of the trial at the
2011 ASCO Annual Meeting.1
Atzpodien Regimen
Previous
studies demonstrated high response rates with the combination of
interleukin-2, interferon alfa, and 5-FU as first-line therapy in
patients with metastatic renal cell carcinoma. Known as the
Atzpodien regimen (after Dr. Jens Atzpodien, who developed it), the
combination was considered the optimal adjuvant therapy in 1995,
when the present trial was initiated. This EORTC/NCRI study funded
by CR-UK was designed to determine if adjuvant therapy with the
Atzpodien regimen improves survival compared with observation alone
in patients who are at high risk of relapse following
nephrectomy.
Patients were eligible
for this randomized phase III trial if they were 8 weeks
postnephrectomy with no macroscopic residual disease, had stage
T3b-c, T4, or any pT and pN1 or pN2 or positive microscopic margins
or microscopic vascular invasion, and had no metastases. The trial
was designed to detect an increase in 3-year disease-free survival
from 50% in the control arm to 65% with treatment (HR = 0.63),
with 90% power and 2-sided alpha of 0.05. Quality of life was
assessed using the EORTC QLQ C-30 instrument.
No Significant
Differences
A total of 309 patients
were enrolled in the trial (68% male), including 155 on the control
arm (median age, 55 years) and 154 on the treatment arm (median
age, 57 years). However, 35% of patients who received the
combination regimen were unable to complete therapy, largely due to
treatment-related toxicity (at least grade 2 in 92% of patients,
and at least grade 3 in 41%). At 6 months, no statistically
significant differences were observed in any quality-of-life
parameters between the two treatment arms.
With a median follow-up
of 5.9 years (maximum 12.1 years), the investigators found no
statistically significant survival benefit for the treatment
regimen arm compared with the control arm. The 3-year disease-free
survival was 61% on the treatment arm and 50% on the control arm
(overall HR = 0.84; 95% CI = 0.63-1.12). Overall survival at 5
years was also similar (70% vs 63%; HR = 0.86; 95% CI = 0.60-1.22).
Post hoc exploratory analysis suggested a possible difference in
survival between pT1 and pT2 patients, which needs to be confirmed
in additional trials. ■
Disclosure:Dr. Aitchison is a consultant
for and has received honoraria from Novartis and Pfizer. Dr.
Rosenberg is an employee of UBC Scientific Solutions and has
previously provided medical writing support, which was funded by
Pfizer.
Expert
Point of View:
Adjuvant Immunotherapy Provides No Clinical Benefit in Patients
with High‑risk Renal Cell Carcinoma
Reference
1. Aitchison M, Bray CA, Van Poppel H, et al: Final results from
an EORTC (GU Group)/NCRI randomized phase III trial of adjuvant
interleukin-2, interferon alpha, and 5-fluorouracil in patients
with a high risk of relapse after nephrectomy for renal cell
carcinoma (RCC). 2011 ASCO Annual Meeting.
Abstract 4505. Presented June 6, 2011.