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Comparing three induction regimens for nasopharyngeal carcinoma: a propensity score-matched analysis
Jinxuan Dai1, Yu Pan1, Yuanyuan Liu2
1Department of Radiation Oncology, The Second Affiliated Hospital of Guilin Medical University, Guilin, China.
Gemcitabine plus cisplatin (GP) induction chemotherapy shows superior overall survival for locoregionally advanced nasopharyngeal carcinoma (LA-NPC). The GP regimen offers a favorable safety profile, making it a clinically advantageous option compared to TPF and TP regimens.
Area of Science:
- Oncology
- Medical Research
- Clinical Trials
Background:
- Locoregionally advanced nasopharyngeal carcinoma (LA-NPC) is a challenging diagnosis.
- Induction chemotherapy (IC) regimens, including gemcitabine plus cisplatin (GP), docetaxel plus cisplatin plus fluorouracil (TPF), and paclitaxel plus cisplatin (TP), are established treatment options.
Purpose of the Study:
- To compare the efficacy and toxicity of GP, TPF, and TP induction chemotherapy regimens in patients with LA-NPC.
- To evaluate survival outcomes and acute toxicities associated with these IC regimens.
Main Methods:
- A multicenter retrospective study involving 722 patients with stage III-IVA LA-NPC.
- Propensity score matching (PSM) was utilized to balance baseline characteristics before comparing outcomes.
- Survival endpoints included overall survival (OS), failure-free survival (FFS), local recurrence-free survival (LRFS), and distant metastasis-free survival (DMFS).
Main Results:
- After PSM, the GP group demonstrated a significantly better 3-year OS rate compared to the TP group (p=0.019).
- No significant differences in 3-year OS were observed between the GP and TPF groups, or between the TPF and TP groups.
- There were no significant differences in 3-year FFS, LRFS, or DMFS rates among the three regimens. Toxicity profiles were generally acceptable and manageable.
Conclusions:
- The gemcitabine plus cisplatin (GP) induction regimen exhibits superior efficacy in overall survival for LA-NPC patients.
- GP offers a favorable safety profile, positioning it as a more clinically advantageous treatment option compared to TPF and TP regimens.
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