Abstract 80P
Background
Analysis of the intent-to-treat (ITT) population of RATIONALE-302 (NCT03430843) found overall HRQoL, fatigue, and physical functioning were maintained in patients (pts) receiving tislelizumab, while worsening in pts receiving investigator-chosen chemotherapy (ICC). Post-hoc analysis examines HRQoL and ESCC symptoms in the Asian and non-Asian subgroups of pts in RATIONALE-302.
Methods
Patients with advanced or metastatic ESCC that progressed following systemic therapy were randomized 1:1 to receive either tislelizumab or ICC (paclitaxel, docetaxel, or irinotecan). HRQoL was measured using the EORTC QLQ-C30 and the QLQ-OES18. Least-squares mean score change from baseline to weeks 12 and 18 in HRQoL scores was assessed using a mixed model for repeated measurements. Reported nominal p-values are for descriptive purpose only.
Results
Of the total of 512 pts, this analysis was conducted in the subgroup of 392 Asian pts (tislelizumab N=192; ICC N=200). Tislelizumab pts had stable GHS/QoL, while fatigue scores worsened in both arms, though more so in ICC pts. Change from baseline was similar in both arms for physical functioning at weeks 12 and 18. The eating score remained stable in tislelizumab pts, while it worsened in ICC pts, particularly at week 18. Reflux improved at week 12 in the tislelizumab pts and worsened in ICC pts. Of note, a similar pattern of results was found in the smaller non-Asian subgroup (tislelizumab N=49; ICC N=47). Table: 80P
Least-squares (LS) mean change from baseline in Asian subgroup
Week 12 LS mean change tislelizumab vs ICC | Week 18 LS mean change tislelizumab vs ICC | ||
QLQ-30 | |||
GHS/QoL | 0.01 vs -5.9, p=0.032 | -0.8 vs -9.8, p=0.0011 | |
Physical functioning | -3.7 vs -5.7, p=0.2941 | -3.7 vs -6.5, p=0.1492 | |
Fatigue | 4.0 vs 10.3, p=0.0149 | 1.8 vs 7.0, p=0.0815 | |
OES18 | |||
Eating | 0.1 vs 3.3, p=0.1444 | 0.8 vs 5.8, p=0.0818 | |
Reflux | -2.3 vs 3.3, p=0.0068 | -2.3 vs -1.2, p=0.6978 |
Conclusions
The HRQoL and ESCC-related symptoms of the Asian subgroup of tislelizumab pts remained stable or improved while ICC pts experienced worsening. These HRQoL results in Asian pts corroborate the HRQoL findings in the total population, suggesting tislelizumab is a potential new second-line treatment option for pts with advanced or metastatic ESCC.
Clinical trial identification
Editorial acknowledgement
Writer: Jason C. Allaire, Generativity.
Legal entity responsible for the study
BeiGene.
Funding
BeiGene.
Disclosure
S. Kim: Financial Interests, Personal, Advisory Role: Novartis, AstraZeneca, Lilly, Dae Hwa Pharmaceutical Co. Ltd., ISU Abxis, Daiichi-Sankyo; Financial Interests, Personal, Leadership Role: ESMO Breast 2021; Financial Interests, Personal, Stocks/Shares: Genopeaks, NeogeneTC; Financial Interests, Personal, Research Grant: Novartis, Sanofi-Aventis, DongKook Pharm Co. E. Van Cutsem: Financial Interests, Personal, Advisory Role: Bayer, Lily, Roche, Servier, Bristol Myers Squibb, Celgene, Merck Sharp & Dohme, Merck KGaA, Novartis, AstraZeneca, Halozyme, Array BioPharma, Biocartis, GlaxoSmithKline, Daiichi Sankyo, Pierre Fabre, Sirtex Medical, Taiho Pharmaceutical, Incyte, Astellas Pharma; Financial Interests, Institutional, Research Grant: Amgen, Bayer, Boehringer Ingelheim, Lilly, Novartis, Roche, Celgene, Ipsen, Merck, Merck KGaA, Servier, Bristol Myers Squibb. J.A. Ajani, L. Shen: Financial Interests, Personal, Writing Engagements: BeiGene. G. Barnes: Financial Interests, Personal, Full or part-time Employment: Beigene Ltd.; Financial Interests, Personal, Stocks/Shares: Beigene Ltd. N. Ding: Financial Interests, Personal, Full or part-time Employment: BeiGene. T. Xia: Financial Interests, Personal, Full or part-time Employment: BeiGene; Financial Interests, Personal, Stocks/Shares: BeiGene. L. Zhan: Financial Interests, Personal, Full or part-time Employment: BeiGene; Financial Interests, Personal, Stocks/Shares: BeiGene. K. Kato: Financial Interests, Personal, Writing Engagements: BeiGene; Financial Interests, Personal, Sponsor/Funding: ONO, BMS, MSD, Shionogi, Beigene, Chugai, Astra Zeneca, BAYER, Oncolys Biopharma; Financial Interests, Personal, Advisory Role: BMS, MSD; Financial Interests, Personal, Invited Speaker: ONO, BMS, Eli Lilly, Taiho. All other authors have declared no conflicts of interest.
Resources from the same session
48P - Long-term clinical outcomes after the second metastasectomy in patients (pts) with resected metastatic colorectal cancer (mCRC)
Presenter: Songji Choi
Session: Poster viewing 02
49P - Ramucirumab beyond progression plus TAS 102 in patients with advanced or metastatic adenocarcinoma of the stomach or the gastroesophageal junction, after treatment failure on a ramucirumab based therapy: Final results of the phase II RE-ExPEL study
Presenter: Thorsten Goetze
Session: Poster viewing 02
50P - Linear tumor regression of rectal cancer in daily MRI during preoperative chemoradiotherapy: An insight of tumor regression velocity for personalized cancer therapy
Presenter: Sea-Won Lee
Session: Poster viewing 02
51P - Efficacy and safety of sintilimab as first-line therapy in patients with microsatellite instability-high metastatic colorectal cancer: A real-world study
Presenter: Caiyun Nie
Session: Poster viewing 02
53P - Baseline PET/CT deep radiomics signature apply for identifying bevacizumab sensitivity of RAS-mutant colorectal cancer liver metastases patients
Presenter: Wenju Chang
Session: Poster viewing 02
54P - Efficacy of total neoadjuvant therapy (TNT) in rectal cancer: A meta-analysis of randomized controlled trials
Presenter: Yakup Ergün
Session: Poster viewing 02
55P - Biodegradable and biocompatible 3D-printed scaffolds loaded with chemotherapy drugs: A new horizon for treatment of colon cancer with diffuse intraperitoneal metastasis
Presenter: Amirhosein Kefayat
Session: Poster viewing 02
56P - Clinico-pathological profile of adolescent and young adult colorectal cancer patients: Multicentre collaborative registry data from India
Presenter: Soumya Surath Panda
Session: Poster viewing 02