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What is the value of third-line chemotherapy in advanced gastroesophageal cancer? A 5-year retrospective analysis at a single center.

Authors :
Lam JYC
Choo SP
Tai DW
Tan IBH
Tham CK
Koo WH
Ong SYK
Ang SF
Chua CWL
Chong DQ
Teo PTH
Lee CJZ
Ee SCE
Ng MCH
Source :
Asia-Pacific journal of clinical oncology [Asia Pac J Clin Oncol] 2020 Feb; Vol. 16 (1), pp. 23-27. Date of Electronic Publication: 2019 Nov 17.
Publication Year :
2020

Abstract

Aim: The survival benefit of using a non-cross resistant second-line chemotherapy in the third-line setting in metastatic gastroesophageal cancer is unproven. We evaluated the utility of third-line chemotherapy in patients treated at a single institution.<br />Methods: Between 2010 and 2014, efficacy and toxicity data of patients who received three or more lines of systemic therapies for metastatic gastroesophageal adenocarcinoma at the National Cancer Centre Singapore was retrospectively analyzed.<br />Results: Thirty-two (6%) patients received three or more lines of chemotherapy. The median age and ECOG performance status were 59 years (36-82) and 1 (0-2), respectively. Majority of patients (88%) had tumor located in the stomach and 13 patients (41%) had diffuse histology or poorly cohesive or signet ring cells. Four (12%) patients had HER2-positive disease. Prior therapy was platinum (100%), fluoropyrimidine (97%), taxane (63%), irinotecan (28%), anthracycline (13%) and ramucirumab (3%). Third-line therapy consisted of 24 (75%) monotherapy, 6 (19%) doublet, 1 (3%) triplet chemotherapy and 1 (3%) clinical trial. Monotherapy irinotecan (44%) was most common, followed by docetaxel (19%) and paclitaxel (9%). Of 22 patients evaluable for response, there was 1 (5%) partial response, 9 (41%) stable disease. Median overall survival was 18.3 weeks (4.3-65.1). Of 30 patients evaluable for toxicities, 17 (57%) experienced at least one grade 3 or 4 toxicities.<br />Conclusion: The benefit of using non-cross resistant second-line regimens as third-line chemotherapy was small with moderate toxicity. Newer agents such as nivolumab or TAS-102 or clinical trial may be preferred.<br /> (© 2019 John Wiley & Sons Australia, Ltd.)

Details

Language :
English
ISSN :
1743-7563
Volume :
16
Issue :
1
Database :
MEDLINE
Journal :
Asia-Pacific journal of clinical oncology
Publication Type :
Academic Journal
Accession number :
31736219
Full Text :
https://doi.org/10.1111/ajco.13285