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No Overall Survival Difference for Immediate vs Deferred Chemotherapy After Radical Cystectomy in Muscle-Invasive Bladder Cancer

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Key Points

  • No significant difference in overall survival was observed between immediate and delayed chemotherapy.
  • Immediate treatment was associated with better median and 5-year progression-free survival.

In the phase III EORTC 30994 trial reported in The Lancet Oncology, Sternberg et al found no overall survival difference between immediate and delayed adjuvant chemotherapy after radical cystectomy in patients with muscle-invasive urothelial carcinoma of the bladder. Immediate treatment was associated with improved median and 5-year progression-free survival. The trial was closed due to slow recruitment after enrollment of 284 of a planned 660 patients but may be the largest randomized trial in this setting to date.

Study Details

In this open-label trial, 284 patients from 12 countries in Europe (n = 272) or Canada with pT3 to pT4 or N+ M0 disease after radical cystectomy and bilateral lymphadenectomy and no evidence of microscopic residual disease were randomly assigned within 90 days of cystectomy, between April 2002 and August 2008, to receive immediate chemotherapy (n = 141) or chemotherapy delayed until relapse (n = 143). Immediate chemotherapy consisted of four cycles of gemcitabine plus cisplatin, high-dose methotrexate, vinblastine, doxorubicin, and cisplatin (high-dose MVAC), or MVAC; deferred chemotherapy consisted of six cycles of treatment. The primary endpoint was overall survival in the intention-to-treat population.

Overall, patients had a median age of 61 years, 80% were male, 61% had pT3 disease, 17% had pT4 disease, and 70% had pN+ disease. In the immediate and deferred groups, 18% and 19% were pN− based on < 15 dissected nodes, 12% in both groups were pN− based on ≥ 15 nodes, 43% and 46% were pN+ based on < 15 nodes, and 28% and 23% were pN+ based on ≥ 15 nodes. The median time from cystectomy to randomization was 63 days.

Treatment Received

In total, 195 patients received chemotherapy, which consisted of gemcitabine plus cisplatin in 165 (85%). In the immediate treatment group, treatment was started in 128 (91%) of 141 patients, with 28 receiving fewer than four cycles. Among patients in the deferred treatment group, three (2%) requested and received immediate chemotherapy, 64 (45%) started deferred chemotherapy at the time of disease progression, and 76 (53%) never started deferred treatment; of the latter, 53 (70%) did not exhibit disease progression. Among the 64 patients who received deferred treatment, 44% received fewer than six cycles.  

Overall Survival

Data cutoff was in August 2013. After a median follow-up of 7.0 years (interquartile range = 5.2–8.7 years), 66 patients (47%) in the immediate treatment group and 82 (57%) in the deferred treatment group had died, with death due to bladder cancer occurring in 37% and 45%. Five-year overall survival was 53.6% (95% confidence interval [CI] = 44.5%–61.8%) vs 47.7% (39.1%–55.8%), and median overall survival was 6.74 years (95% CI = 3.85 years–not reached) vs 4.60 years (2.15–6.25 years), yielding an adjusted hazard ratio [HR] of 0.78 (95% CI = 0.56–1.08, P = .13). Five-year mortality due to bladder cancer was 38.6% vs 43.5% (competing risk-adjusted HR = 0.80, P = .22). No significant difference in mortality due to other or unknown causes was observed (competing risk HR = 0.84, P = .61).

Progression-Free Survival

As of the data cutoff, progression or death had occurred in 45% of the immediate treatment group vs 62% of the deferred treatment group, including distant tumor spread at first diagnosis of disease progression in 28% vs 37%. Five-year progression-free survival was 47.6% vs 31.8%, and median progression-free survival was 3.11 years vs 0.99 years (HR =  0.54, P < .0001).

Post-hoc exploratory analyses to assess the effect of treatment according to age, sex, pT category, pN category, pTN category, and time from cystectomy to randomization showed a significant interaction for pN category (pN− vspN+, P = .026 for interaction) for overall survival and no significant interactions for progression-free survival. A significant interaction for overall survival by extent of lymph node sampling was also observed (P = .028 for interaction), but interpretation of the finding is unclear due to the small numbers of patients in the subcategories.

By Lymph Node Involvement

Five-year overall survival was 79.5% vs 59.0% (HR = 0.37, P = .012) in patients without lymph node involvement at baseline and 42.7% vs 42.9% (HR = 0.94, P = .72) in those with lymph node involvement at baseline.

A second primary cancer or myelodysplastic syndrome occurred in 1% vs 7% of patients.

Toxicity

Grade 3 or 4 myelosuppression occurred in 26% of 128 patients who received treatment in the immediate group and 35% of 68 who received treatment in the deferred group, including neutropenia in 38% and 53%, thrombocytopenia in 28% and 38%, and anemia in 8% and 16%. A cycle of treatment was postponed for a maximum of 2 weeks due to adverse events in 59% and 70%, dose reduction occurred in 51% and 78%, and treatment was discontinued due to adverse events in 11% and 10%. Death due to toxicity occurred in two patients: one in the immediate group (neutropenic sepsis) and one in the deferred group (unknown cause 2 weeks after completing treatment).

The investigators concluded: “Our data did not show a significant improvement in overall survival with immediate vs deferred chemotherapy after radical cystectomy and bilateral lymphadenectomy for patients with muscle-invasive urothelial carcinoma. However, the trial is limited in power, and it is possible that some subgroups of patients might still benefit from immediate chemotherapy. An updated individual patient data meta-analysis and biomarker research are needed to further elucidate the potential for survival benefit in subgroups of patients.”

Cora N. Sternberg, MD, of San Camillo and Forlanini Hospitals, Rome, is the corresponding author for The Lancet Oncology article.

The study was funded by Lilly and Canadian Cancer Society Research. For full disclosures of the study authors, visit www.thelancet.com.

The content in this post has not been reviewed by the American Society of Clinical Oncology, Inc. (ASCO®) and does not necessarily reflect the ideas and opinions of ASCO®.


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