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Lung Cancer: Lung Cancer I |

Efficacies and Adverse Reactions of Modified Vitamin Supplement Programs Before Pemetrexed Chemotherapy as a Second-Line Treatment Against Epidermal Growth Factor Receptor (EGFR) Mutant Wild-Type Lung Adenocarcinoma FREE TO VIEW

Chengzhi Zhou, MD; Yinyin Qin, PhD; Shiyue Li, PhD; Rongchang Chen, PhD; Nanshan Zhong, PhD
Author and Funding Information

State Key Laboratory of Respiratory Diseases, National Clinical Research Center of Respiratory Diseases, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou Institute of Respiratory Diseases, Guangzhou, China


Copyright 2016, American College of Chest Physicians. All Rights Reserved.


Chest. 2016;149(4_S):A292. doi:10.1016/j.chest.2016.02.304
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SESSION TITLE: Lung Cancer I

SESSION TYPE: Original Investigation Poster

PRESENTED ON: Saturday, April 16, 2016 at 11:45 AM - 12:45 PM

PURPOSE: This study aims to observe the efficacies and adverse reactions of modified vitamin programs before pemetrexed chemotherapy (second-line treatment) against epidermal growth factor receptor (EGFR) mutant wild-type lung adenocarcinoma.

METHODS: 477 patients with IIIB, phase IV glomerular filtration rate (GFR) mutant-negative lung adenocarcinomas and performed pemetrexed chemotherapy were collected and divided into group A (167 cases, with modified program) and group B (310 cases, with traditional program). The modified program was: orally administrated 400 μg folic acid once per day and 1 day before the first-round pemetrexed chemotherapy, until the 21st day of the final administration of pemetrexed, and intramuscularly injected 500 μg vitamin B12 1 day before the first-round pemetrexed chemotherapy, and injected once 1 day before every round pemetrexed treatment.

RESULTS: Comparison between group A and group B: mean chemotherapy cycles (4.08 vs 3.98); effectiveness rate (22.16% vs 22.90%); disease control rate (56.51% vs 55.00%); without significant difference (P > 0.05). Two groups currently all reached the median overall survival (OS). The median progression-free survival (PFS): 4.2 vs 4.1 months; OS: 12.9 vs 13.2 months, without statistical difference (P > 0.05). Such side effects between the two groups as leukopenia, neutropenia, thrombocytopenia, anemia, nausea, vomiting, diarrhea, fatigue, creatinine increasing, alanine transaminase (ALT) increasing, stomatitis, peripheral neuropathy, alopecia and rash had no significant difference (P > 0.05).

CONCLUSIONS: The modified vitamin supportive treatment could ensure the efficacy, significantly simplify, facilitate the clinical application, and increase the associated toxicities, indicating that the pemetrexed-based chemotherapy did not need to be delayed because applying the vitamin supportive treatment.

CLINICAL IMPLICATIONS: This study made up the shortcomings of previous analytical researches to some extent, significantly simplified and clarified the specific dose and timing of vitamin applications.it could avoid that the best treatment time was delayed because of the vitamin supplementary therapy.

DISCLOSURE: The following authors have nothing to disclose: Chengzhi Zhou, Yinyin Qin, Shiyue Li, Rongchang Chen, Nanshan Zhong

No Product/Research Disclosure Information


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