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Poster display session: Basic science, Endocrine tumours, Gastrointestinal tumours - colorectal & non-colorectal, Head and neck cancer (excluding thyroid), Melanoma and other skin tumours, Neuroendocrine tumours, Thyroid cancer, Tumour biology & pathology

869 - Evaluate the Role of Induction Chemotherapy in the Treatment of Stage II Nasopharyngeal Carcinoma in Intensity Modulated Radiotherapy Era

Date

21 Oct 2018

Session

Poster display session: Basic science, Endocrine tumours, Gastrointestinal tumours - colorectal & non-colorectal, Head and neck cancer (excluding thyroid), Melanoma and other skin tumours, Neuroendocrine tumours, Thyroid cancer, Tumour biology & pathology

Topics

Tumour Site

Head and Neck Cancers

Presenters

Ting Jin

Citation

Annals of Oncology (2018) 29 (suppl_8): viii372-viii399. 10.1093/annonc/mdy287

Authors

T. Jin, P. Li

Author affiliations

  • Radiation Department, Zhejiang Cancer Hospital, 310022 - Hangzhou/CN

Resources

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Abstract 869

Background

While the combined modality treatment of concurrent chemoradiotherapy (CCRT) with or without adjuvant chemotherapy has now been accepted as the standard treatment for advanced Nasopharyngeal carcinoma (NPC), induction chemotherapy +concurrent chemoradiotherapy (ICRT) is commonly used as well. The prognosis of II NPC patients is favorable. We should be more mindful to living quality during/after treatment, length of hospital stay, treatment cost and so forth. Therefore, the purpose of this study is to contrast prognosis of stage II NPC patients underwent the following two treatment modalities: ICRT vs CCRT.

Methods

173 patients with American Joint Committee on Cancer 7th stage II NPC are included and divided into two groups: ICRT and CCRT. Induction chemotherapy consisted of 1 to 3 cycles of cisplatin plus fluorouracil or paclitaxel plus cisplatin. Concurrent chemotherapy includes cisplatin only. We retrospectively assess overall survival (OS), progression-free survival (PFS), locoregional free survival (LRFS) and distant metastasis free survival (DMFS).

Results

With a median follow up of 64.7 months, no significant differences are found in grade 3–4 hematologic toxicity, liver dysfunction and renal impairment between ICRT and CCRT groups. Univariable analyses show adding induction chemotherapy to CCRT significantly decreases 5-year OS (87.9% vs 95.5%, P = 0.033), PFS (74.0% vs 86.1%, P = 0 .035), LRFS (80.0% vs 91.2%, P = 0.016), but there is no statistically significant difference in DMFS (87.1% vs 94.7%, P = 0.095). In multivariable analyses, we find the consistent results that induction chemotherapy is a negative factor associated with OS (HR of death =3.768, 95% CI = 1.117 to 12.709; P = 0.032), PFS (HR of progression = 2.156, 95% CI = 1.060 to 4.386; P = 0.034), LRFS (HR of locoregional relapse = 2.435, 95% CI = 1.009 to 5.874; P = 0.048) and also DMFS (HR of metastasis = 2.873, 95% CI = 1.005 to 8.211; P = 0.049), in stage II NPC patients.

Conclusions

In present study, we find that induction chemotherapy causes deleterious effect on stage II NPC patients. However, this is a retrospective study and the adverse effects of induction chemotherapy has not been previously reported. It warrants further investigation.

Clinical trial identification

Legal entity responsible for the study

Zhejiang Cancer Hospital.

Funding

Has not received any funding.

Editorial Acknowledgement

The authors indicated no potential conflicts of interest.

Disclosure

All authors have declared no conflicts of interest.

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