Recently, the phase 3 CASPIAN trial (NCT03043872) demonstrated first-line treatment of ES-SCLC with durvalumab plus etoposide to improve OS versus etoposide alone (HR 0.73; P=0.0047) [1]. This benefit was sustained with more than 2 years follow-up [2]. In addition, a numerical, not statistically significant improvement in OS was observed with durvalumab plus tremelimumab plus etoposide versus etoposide alone [2].
Updated OS results of CASPIAN after a median of more than 3 years follow-up were presented by Dr Luis Paz-Ares (Hospital Universitario 12 de Octubre, Spain). In CASPIAN, 805 patients with treatment-naïve ES-SCLC were randomised 1:1:1 to durvalumab/etoposide (every 3 weeks), durvalumab/tremelimumab/etoposide (every 3 weeks), or etoposide (every 3 weeks, 6 cycles). Patients in the immunotherapy arms received 4 cycles of etoposide/durvalumab ± tremelimumab, followed by maintenance durvalumab (every 4 weeks). The primary endpoints were OS for durvalumab/etoposide versus etoposide and for durvalumab/tremelimumab/etoposide versus etoposide.
At a median follow-up of 39.4 months (86% maturity), durvalumab/etoposide continued to demonstrate improved OS versus etoposide (HR 0.71; P=0.0003). Median OS was 12.9 versus 10.5 months. At 24 months, 22.9% versus 13.9% of patients were alive, and at 36 months 17.6% versus 5.8% of patients were alive with durvalumab/etoposide versus etoposide, respectively (see Figure).
Figure: 3-year overall survival update of CASPIAN [3]
Durvalumab/tremelimumab/etoposide also continued to improve OS versus etoposide (HR 0.81; P=0.02). Median OS was 10.4 months versus 10.5 months. At 24 months, 22.9% versus 13.9% of patients were alive, and at 36 months 15.3% and 5.8% of patients were alive with durvalumab/tremelimumab/etoposide versus etoposide alone, respectively.
Safety profiles were consistent with previous analyses. “Three times more patients were estimated to be alive at 3 years follow-up when treated with durvalumab/etoposide versus etoposide alone, further establishing durvalumab/etoposide as standard of care for first-line treatment of ES-SCLC,” concluded Dr Paz-Ares. “Addition of tremelimumab to durvalumab/etoposide does not further improve OS.”
- Paz-Ares L, et al. 2019;394:1929-1939.
- Goldman JW, et al. Lancet Oncol. 2021;22:51–65.
- Paz-Ares L, et al. Durvalumab ± tremelimumab + platinum-etoposide in first-line extensive-stage SCLC (ES-SCLC): 3-year overall survival update from the phase III CASPIAN study. Abstract LBA61, ESMO Congress 2021, 16–21 September.
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Table of Contents: ESMO 2021
Featured articles
Breast Cancer
Trastuzumab deruxtecan triples PFS
Novel conjugate meets primary endpoint
Longest survival benefit from first-line CDK4/6 inhibitor
Meta-analysis shows 6-months adjuvant trastuzumab is optimal
Double-positive results for triple-negative metastatic breast cancer
Survival after neoadjuvant therapy with trastuzumab-lapatinib plus chemotherapy
Postmenopausal breast cancer: extended letrozole reduces recurrence
Asian women also benefit from palbociclib plus letrozole
No PEARLs of survival with palbociclib plus endocrine therapy compared with capecitabine, but QoL better
Gastrointestinal Cancer
Neoadjuvant chemotherapy potential alternative to neoadjuvant chemoradiotherapy in LARC
Immune chemo-sensitisation looks promising in microsatellite-stable mCRC
Adagrasib shows promising clinical activity in heavily pretreated KRAS-mutated CRC
Automated detection of microsatellite status on unstained samples in early colon cancer
Consistent benefit of anti-PD-1 therapy for oesophageal and gastric cancer
HIPEC in gastric cancer with peritoneal metastases
ctDNA highly predictive in HER2-positive, advanced gastric or gastro-oesophageal junction cancer
Lung Cancer
Robust anticancer activity of trastuzumab deruxtecan in HER2-mutated NSCLC
Nivolumab/ipilimumab continues to provide survival benefit in unresectable MPM
Adjuvant atezolizumab lowers relapse rate in resected NSCLC
Three-year OS follow-up from CASPIAN trial
TCR clonality predicts pembrolizumab response in NSCLC
Melanoma
Adjuvant immunotherapy reduces risk of disease recurrence in stage II melanoma
IFN-γ signature predicts response to immunotherapy
Updated results of SECOMBIT trial
Combining T-VEC and pembrolizumab does not significantly improve survival in advanced, unresectable melanoma
Durable intracranial responses with nivolumab/ipilimumab
Genitourinary Cancer
TKI drug-free interval strategy not detrimental to conventional continuation strategy in RCC
Modified ipilimumab schedule reduces risk of grade 3/4 adverse events
Optimal neoadjuvant dose ipilimumab/nivolumab in stage III urothelial cancer
Better survival with neoadjuvant dose-dense MVAC regimen in MIBC
PARP inhibitor rechallenge improves PFS in ovarian cancer
Pembrolizumab prolongs survival in persistent, recurrent, or metastatic cervical cancer
Pembrolizumab has durable effect in previously treated MSI-H/dMMR advanced endometrial cancer
HRR mutational status is prognostic and predictive biomarker olaparib activity
Haematological Cancer
Mutational analyses are predictive in malignant lymphomas
Low numbers of M2 macrophages in tumour microenvironment associated with superior response to immunotherapy in Hodgkin lymphoma
COVID-19
Adequate response to SARS-CoV-2 vaccine in cancer patients
Cancer patients more likely to die from COVID-19 when hospital admittance is required
Third global survey of the ESMO Resilience Task Force
High COVID-19 mortality in Swiss cancer patients
Basic Science & Translational Research
Neutrophils negatively correlate with response to anti-PD-1 monotherapy in dMMR tumours
Tetraspecific ANKETs harnesses innate immunity in cancer therapies
Early ctDNA reduction in metastatic uveal melanoma correlates better with OS than RECIST response
Gut microbiota as a potential predictive biomarker
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