Outcomes in older adults with metastatic esophageal and gastric carcinoma treated with palliative chemotherapy

Author:

Wang Xin1ORCID,Allen Michael J1ORCID,Espin-Garcia Osvaldo2,Suzuiki Chihiro1,Bach Yvonne1,Panov Elan1,Ma Lucy X1,Jang Raymond W1,Chen Eric X1,Darling Gail E3,Yeung Jonathan3ORCID,Swallow Carol J45,Brar Savtaj Singh5,Kalimuthu Sangeetha6,Wong Rebecca7,Veit-Haibach Patrick8,Elimova Elena1

Affiliation:

1. Division of Medical Oncology, Princess Margaret Cancer Centre, University Health Network , Toronto ON , Canada

2. Department of Biostatistics, Princess Margaret Cancer Centre, University Health Network , Toronto, ON , Canada

3. Division of Thoracic Surgery, Toronto General Hospital, University Health Network , Toronto ON , Canada

4. Department of Surgical Oncology, Princess Margaret Cancer Centre, University Health Network , Toronto ON , Canada

5. Department of Surgery, Mount Sinai Hospital , Toronto , ON, Canada

6. Division of Pathology, Toronto General Hospital, University Health Network , Toronto ON , Canada

7. Division of Radiation Oncology, Princess Margaret Hospital, University Health Network , Toronto ON , Canada

8. Joint Department of Medical Imaging, Toronto General Hospital, University Health Network , Toronto ON , Canada

Abstract

Abstract Background The incidence of esophageal and gastric carcinoma (GEC) in elderly patients is increasing, yet patients ≥75 years have historically been underrepresented in clinical trials. We sought to investigate palliative chemotherapy administration patterns and survival outcomes in older adults. Materials and Methods A retrospective analysis identified patients aged 65-74 (young-old) and ≥75 years (older-old) diagnosed with advanced GEC. Patient and tumor characteristics were recorded, with descriptive analysis, time-to-event data analysis using Kaplan-Meier curves and multivariate Cox proportional hazards regression analysis performed. Results One hundred and ninety-eight “young-old” and 109 ‘older-old’ patients were identified. Patient characteristics were similar between groups except for Charlson Co-morbidity Index (CCI), with lower co-morbidities in the “young-old” compared to “older-old” cohort (P < .001; CCI = 0 in 103 (52%) “young-old” vs 31 (28%) “older-old”). The primary diagnosis in both groups was adenocarcinoma. 119 (60%) “young-old” and 25 (23%) “older-old” patients received chemotherapy (P < .001). Performance status was the primary explanation for chemotherapy non-receipt in both cohorts; age was the explanation in 21 (25%) “older-old” patients and none in the “young-old” patients. PFS for first-line systemic therapy in “young-old” patients was 6.4 (95% CI 5.9-7.6) versus 7.5 months (95% CI 5.1-11.3) in “older-old” patients (P = .69) whilst respective OS was 12.3 (95% CI 10.1-15.5) and 10.4 months (95% CI 9.0-14.6) (P = .0816). Toxicity prompted chemotherapy cessation in 17 (15%) “young-old” and 3 (13%) “older-old” patients (P = .97). Multivariate analysis identified CCI and ECOG performance status as predictive for PFS and OS, respectively. No causative relationship was identified with other variables. Conclusion Our study of real-world older-adults show that significant number of “older-old” patients with GEC do not receive chemotherapy. Among “older-old” adults who do receive systemic therapy, outcomes are comparable; this underscores the importance of geriatric assessment-guided care and suggests that age alone should not be a barrier to receipt of chemotherapy in patients with advanced GEC.

Publisher

Oxford University Press (OUP)

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