File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.ijrobp.2017.11.038
- Scopus: eid_2-s2.0-85044354958
- PMID: 29413277
- WOS: WOS:000425035400020
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Prospective, Multicenter, Phase 2 Trial of Induction Chemotherapy Followed by Bio-Chemoradiotherapy for Locally Advanced Recurrent Nasopharyngeal Carcinoma
Title | Prospective, Multicenter, Phase 2 Trial of Induction Chemotherapy Followed by Bio-Chemoradiotherapy for Locally Advanced Recurrent Nasopharyngeal Carcinoma |
---|---|
Authors | |
Issue Date | 2018 |
Publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/ijrobp |
Citation | International Journal of Radiation Oncology - Biology - Physics, 2018, v. 100 n. 3, p. 630-638 How to Cite? |
Abstract | Purpose:
To evaluate, in a phase 2 study, whether induction docetaxel, cisplatin, and fluorouracil (TPF) followed by weekly docetaxel and cetuximab in concurrence with intensity modulated radiation therapy can improve the treatment outcome for patients with advanced locally recurrent nasopharyngeal carcinoma (rNPC).
Methods and Materials:
Thirty-three patients with rNPC (T3-T4, N0-N1, M0) were recruited. Of these, 19 patients (57.6%) had stage rT3 recurrence, and the rest had stage rT4. Eight patients also had rN1 at the time of relapse. Treatment outcomes and safety were evaluated.
Results:
Among these 33 patients, 1 died after 1 cycle of TPF, 5 patients withdrew from the study during the induction period because of grade ≥3 toxicities; 27 patients completed the whole course of treatment, but 1 died before any assessment could be made. The median follow-up period was 28.5 months. The progression-free survival and overall survival at 3 years for the whole group were 35.7% and 63.8%, respectively. Among the 26 patients who could be assessed after treatment, the complete response rate was 30.8%, and the locoregional control rate at 3 years was 49.2%. Temporal lobe necrosis (TLN) developed in 8 cases. The rates of grade ≥3 hearing loss, soft tissue necrosis, dysphagia, and trismus were 30.8%, 15.4%, 11.5%, and 19.2%, respectively. Overall, 5 patients died owing to acute (1 after cycle 1 TPF and 1 after completion of bio-chemoradiotherapy) or late (2 epistaxis and 1 TLN) treatment-related complications.
Conclusions:
The proposed salvage treatment regimen for advanced locally recurrent NPC could achieve a better treatment outcome than seen in previous studies. However, poor tolerability of induction TPF and the high rate of TLN limit its applicability outside clinical trials. |
Persistent Identifier | http://hdl.handle.net/10722/251421 |
ISSN | 2023 Impact Factor: 6.4 2023 SCImago Journal Rankings: 1.992 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ng, WT | - |
dc.contributor.author | Ngan, KC | - |
dc.contributor.author | Kwong, DLW | - |
dc.contributor.author | Tung, SY | - |
dc.contributor.author | Yuen, KT | - |
dc.contributor.author | Kam, MKM | - |
dc.contributor.author | Sze, HCK | - |
dc.contributor.author | Yiu, HHY | - |
dc.contributor.author | Chan, LLK | - |
dc.contributor.author | Lung, ML | - |
dc.contributor.author | Lee, AWM | - |
dc.date.accessioned | 2018-03-01T03:39:00Z | - |
dc.date.available | 2018-03-01T03:39:00Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | International Journal of Radiation Oncology - Biology - Physics, 2018, v. 100 n. 3, p. 630-638 | - |
dc.identifier.issn | 0360-3016 | - |
dc.identifier.uri | http://hdl.handle.net/10722/251421 | - |
dc.description.abstract | Purpose: To evaluate, in a phase 2 study, whether induction docetaxel, cisplatin, and fluorouracil (TPF) followed by weekly docetaxel and cetuximab in concurrence with intensity modulated radiation therapy can improve the treatment outcome for patients with advanced locally recurrent nasopharyngeal carcinoma (rNPC). Methods and Materials: Thirty-three patients with rNPC (T3-T4, N0-N1, M0) were recruited. Of these, 19 patients (57.6%) had stage rT3 recurrence, and the rest had stage rT4. Eight patients also had rN1 at the time of relapse. Treatment outcomes and safety were evaluated. Results: Among these 33 patients, 1 died after 1 cycle of TPF, 5 patients withdrew from the study during the induction period because of grade ≥3 toxicities; 27 patients completed the whole course of treatment, but 1 died before any assessment could be made. The median follow-up period was 28.5 months. The progression-free survival and overall survival at 3 years for the whole group were 35.7% and 63.8%, respectively. Among the 26 patients who could be assessed after treatment, the complete response rate was 30.8%, and the locoregional control rate at 3 years was 49.2%. Temporal lobe necrosis (TLN) developed in 8 cases. The rates of grade ≥3 hearing loss, soft tissue necrosis, dysphagia, and trismus were 30.8%, 15.4%, 11.5%, and 19.2%, respectively. Overall, 5 patients died owing to acute (1 after cycle 1 TPF and 1 after completion of bio-chemoradiotherapy) or late (2 epistaxis and 1 TLN) treatment-related complications. Conclusions: The proposed salvage treatment regimen for advanced locally recurrent NPC could achieve a better treatment outcome than seen in previous studies. However, poor tolerability of induction TPF and the high rate of TLN limit its applicability outside clinical trials. | - |
dc.language | eng | - |
dc.publisher | Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/ijrobp | - |
dc.relation.ispartof | International Journal of Radiation Oncology - Biology - Physics | - |
dc.title | Prospective, Multicenter, Phase 2 Trial of Induction Chemotherapy Followed by Bio-Chemoradiotherapy for Locally Advanced Recurrent Nasopharyngeal Carcinoma | - |
dc.type | Article | - |
dc.identifier.email | Ng, WT: ngwt1@hkucc.hku.hk | - |
dc.identifier.email | Ngan, KC: rkcngan@hku.hk | - |
dc.identifier.email | Kwong, DLW: dlwkwong@hku.hk | - |
dc.identifier.email | Yuen, KT: ktyuen@hkucc.hku.hk | - |
dc.identifier.email | Sze, HCK: henrysze@graduate.hku.hk | - |
dc.identifier.email | Lung, ML: mlilung@hku.hk | - |
dc.identifier.email | Lee, AWM: awmlee@hkucc.hku.hk | - |
dc.identifier.authority | Ng, WT=rp02671 | - |
dc.identifier.authority | Ngan, KC=rp02371 | - |
dc.identifier.authority | Kwong, DLW=rp00414 | - |
dc.identifier.authority | Sze, HCK=rp01697 | - |
dc.identifier.authority | Lung, ML=rp00300 | - |
dc.identifier.authority | Lee, AWM=rp02056 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.ijrobp.2017.11.038 | - |
dc.identifier.pmid | 29413277 | - |
dc.identifier.scopus | eid_2-s2.0-85044354958 | - |
dc.identifier.hkuros | 284336 | - |
dc.identifier.volume | 100 | - |
dc.identifier.issue | 3 | - |
dc.identifier.spage | 630 | - |
dc.identifier.epage | 638 | - |
dc.identifier.isi | WOS:000425035400020 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0360-3016 | - |