Barcelona, Spain (UroToday.com) Interim results from APACHE have been published, with the monotherapy (durvalumab) arm stopped for futility among patients with refractory germ cell tumors1. The evidence from the durvalumab monotherapy arm were even more negative than that reported for monotherapy pembrolizumab amongst similar patients2. At the European Society of Medical Oncology (ESMO) 2019 Annual Congress, Dr. Fare and colleagues presented updated results of APACHE with the expanded combination therapy cohort.

APACHE is an open-label, randomized, three-stage, Phase II study. Patients who have failed ≥2 chemotherapy regimens received durvalumab 1.5 gr q4w, x 13 cycles (arm A) or durvalumab plus tremelimumab 75 mg q4w, x 4 cycles, followed by durvalumab alone x total 13 cycles (arm B). The primary endpoint was the modified objective response-rate (mORR = RECIST 1.1 complete or partial response or stable disease + serum tumor marker reduction >10%). The null hypothesis was that mORR rate would be ≤10%, and the test hypothesis was that mORR ≥25% (α and β = 10%). The total sample size of 120 patients was split into three stages: in stage 1, each arm was terminated whenever no response was observed in 11 patients/arm. In stage 2, 29 additional patients/arm were enrolled. Biomarker analyses included: PD-L1 expression on immune cells and comprehensive genomic profiling with the FoundationOne assay.

The APACHE study design:

APACHE study design

From February 2017 to November 2018, 29 patients were enrolled (11 arm A and 18 arm B). including 22 with gonadal and 7 with extragonadal germ cell turmors (GCT). There were 19 patients that received ≥3 prior chemotherapy regimens. Median tumor mutational burden was 4 mutations /mb, one patient showed microsatellite instability in arm A. There were 10 patients (34.5%) that experienced any-grade adverse events, without differences between arms. In the expanded arm B, two responses (11.1%, one RECIST-partial response in seminoma and one stable disease with serum tumor marker reduction in nonseminoma) and two stable disease were observed. Progressive disease occurred regardless of PD-L1 expression and tumor mutational burden. After a median follow-up of 16.3 months, the 12-month overall survival (OS) in arm A was 30% (95% CI 7.2-57.7) and in arm B was 29.6% (95% CI 10.2-52.2). Further chemotherapy post-progressive disease was administered in eight patients (27.6%), but was mostly ineffective (7 stable disease, 8 progressive disease).

Swimmers plot for duration of treatment:

swimmers plot for duration of treatment

The conclusions of this updated analysis from APACHE are as follows:

  • Despite objective responses being rare with immunotherapy, long-term OS results are encouraging in very highly pre-treated GCT patients, suggesting a role for maintenance approach in the earlier setting (2nd-line chemotherapy), and using durvalumab + tremelimumab due to more responses
  • Conventional immuno-oncology biomarkers did not allow for patient selection, and further research is warranted.

Clinical Trial Identification: NCT03081923.

Presented by: Elena Farè, MD, Istituto Nazionale dei Tumori di Milano – Fondazione IRCCS, Milan, Italy

Co-Authors: D. Raggi1, P. Giannatempo1, M. Colecchia1, G. Calareso2, S. Ali3, J. Chung3, J. Ross3, A. Necchi1
1. Istituto Nazionale dei Tumori di Milano – Fondazione IRCCS, Milan, IT
2. Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, IT
3. Foundation Medicine, Cambridge, US

Written by: Zachary Klaassen, MD, MSc – Assistant Professor of Urology, Georgia Cancer Center, Augusta University/Medical College of Georgia, Twitter: @zklaassen_md at the 2019 European Society for Medical Oncology annual meeting, ESMO 2019 #ESMO19, 27 Sept – 1 Oct, 2019 in Barcelona, Spain

References: 

  1. Necchi, Andrea, Patrizia Giannatempo, Daniele Raggi, Luigi Mariani, Maurizio Colecchia, Elena Farè, Francesco Monopoli et al. “An open-label randomized phase 2 study of durvalumab alone or in combination with tremelimumab in patients with advanced germ cell tumors (APACHE): results from the first planned interim analysis.” European urology 75, no. 1 (2019): 201.
  2. Adra, Nabil, Lawrence H. Einhorn, Sandra K. Althouse, Natraj R. Ammakkanavar, Dana Musapatika, Costantine Albany, David Vaughn, and Nasser H. Hanna. “Phase II trial of pembrolizumab in patients with platinum refractory germ-cell tumors: a Hoosier Cancer Research Network Study GU14-206.” Annals of Oncology 29, no. 1 (2017): 209-214.
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