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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

5271 - Comparison of 3-weekly cisplatin versus 3-weekly carboplatin in patients with locally advanced nasopharyngeal carcinoma (LA-NPC) receiving concurrent chemoradiotherapy (CCRT) : A multicenter retrospective study

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

Arunee Dechaphunkul

Citation

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

Authors

A. Dechaphunkul1, P. Danchaivijitr2, R. Jiratrachu3, T. Dechaphunkul4, C. Sookthon5, C. Jiarpinitnun6, C. Paoin2, J. Setakornnukul7, S. Niyomnaitham8, B. Suktitipat9, P. Pattaranutaporn6, N. Ngamphaiboon10

Author affiliations

  • 1 Medicine, Division Of Medical Oncology, Prince of Songkla University, 90110 - Hat Yai/TH
  • 2 Medicine, Siriraj Hospital, Mahidol University, 10700 - Bangkok/TH
  • 3 Radiology, Prince of Songkla University, 90110 - Hat Yai/TH
  • 4 Otorhinolaryngology Head And Neck Surgery, Songkhlanagarind Hospital, 90110 - Songkla/TH
  • 5 Medicine, Ramathibodi Hospital, 10400 - Bangkok/TH
  • 6 Radiology, Ramathibodi Hospital, 10400 - Bangkok/TH
  • 7 Radiology, Siriraj Hospital, Mahidol University, 10700 - Bangkok/TH
  • 8 Pharmacology, Siriraj Hospital, Mahidol University, 10700 - Bangkok/TH
  • 9 Biochemistry, Siriraj Hospital, Mahidol University, 10700 - Bangkok/TH
  • 10 Medicine, Division Of Medical Oncology, Ramathibodi Hospital, 10400 - Bangkok/TH

Resources

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Abstract 5271

Background

Although CCRT with high-dose cisplatin remains the standard protocol for patients with LA-NPC, carboplatin has been alternatively used especially for cisplatin-ineligible patients. However, the comparable efficacy of these 2 regimens is still unclear. This study aimed to compare the efficacy and tolerability of 3-weekly carboplatin with 3-weekly cisplatin.

Methods

From May 2005 to November 2014, we retrospectively reviewed medical information for 787 LA-NPC patients treated with CCRT from 3 university hospitals in Thailand. Chemotherapy regimen would be either cisplatin (75-100 mg/m2) or carboplatin (AUC-5 or 6), followed by adjuvant chemotherapy (platinum plus 5-fluorouracil). Tolerability and survival were analyzed and compared.

Results

Patient demographics, baseline characteristics, and treatment for the patients was shown in the table. During CCRT, 52% of patients in the cisplatin arm completed the 3 planned cycles of treatment, compared to 88% in the carboplatin arm (P < 0.0001). Fifty-six percent of patients in the cisplatin, whereas only 5% in the carboplatin arm required dose reduction of chemotherapy due to toxicities (P < 0.0001). At the time of analysis, the 5-year disease-free survival was 60% (95% confidence interval [CI], 56 to 63) and 62% (95% CI, 50 to 72) (P = 0.21), and 5-year overall survival was 74% (95% CI, 70 to 77) and 67% (95% CI, 56 to 77) (P = 0.19), in the cisplatin and carboplatin groups, respectively.Table: 1076P

VariablesTreatment groupP-value
Cisplatin (n = 710)Carboplatin (n = 77)
Median age (years)50480.915
Sex [n (%)] Male500 (70)56 (73)0.391
Smoking Yes [n (%)]225 (32)47 (61)<0.0001
Comorbidity Yes [n (%)]96 (14)18 (23)0.019
Stage I [n (%)] II [n (%)] III [n (%)] IVa-IVb [n (%)]2 (0.3) 110 (15.6) 289 (41) 308 (43)1 (1) 11 (15) 28 (36) 37 (48)0.454
WHO classification I [n (%)] II [n (%)] III [n (%)] Missing [n (%)]5 (0.7) 206 (29) 161 (22.7) 338 (47.6)0 (0) 39 (51) 38 (49) 0 (0)0.401
Median baseline Cr (mg%)0.870.94<0.0001

Conclusions

Carboplatin showed similar efficacy to that of cisplatin with better tolerability and could be used as an alternative regimen.

Clinical trial identification

Legal entity responsible for the study

Research University Network: Head and Neck Working Group.

Funding

Research University Network (Thailand).

Editorial Acknowledgement

Disclosure

All authors have declared no conflicts of interest.

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