Abstract 896P
Background
CRT is the standard-of-care treatment for locoregionally advanced OPSCC. Clinical trials with CRT request CT be given at the beginning of the week (Mon-Wed). However, in clinical practice, patients (pts) undergoing CRT may be given CT any day of the week. The objective of this study was to assess if day of the week of CT during CRT impacts treatment outcomes.
Methods
Retrospective study of 735 OPSCC pts treated with curative-intent CRT at MD Anderson between 2002 and 2013. Clinicopathologic characteristics of both groups were compared by chi-square test and/or Wilcoxon rank-sum test. Time-to-event analysis was conducted by Kaplan-Meier method, log-rank test, and cox proportional hazards model. Primary endpoints were recurrence rate (RR), time to recurrence (TTR), recurrence-free survival (RFS), and overall survival (OS).
Results
Of 735 pts, 648 (88%) were male and 417 (57%) were current or former smokers. For 414 (56%) pts, HPV status was known, with 329 HPV-positive and 39 HPV-negative. The large majority of pts (697, 95%) had base of tongue or tonsil primary site. Most frequent TNM stage by AJCC 7th ed. at diagnosis was T3-T4 (379, 52%) and N2a-N2b (430, 59%). Cisplatin was the most used agent (360, 49%), with CT mostly on a weekly schedule (557, 76%). Most frequent radiation therapy was conventional fractionation (588, 80%) with 545 pts (74%) receiving ≥ 7000 rads. Pts were divided into two groups based on day of the week of CT: Monday/Tuesday/Wednesday (M/T/W; 632, 86%) vs Thursday/Friday (T/F; 103, 14%). Groups were balanced for all clinicopathologic characteristics, except for gender (p=0.03), RT dose received (p=0.04), and CT regimen (weekly vs. every 3 weeks, p<0.0001). There was no significant difference in RR between groups, with M/T/W RR 21% vs T/F RR 29% (p=0.07). Median OS was 155 mo (95%CI 145-NR) with no significant difference between M/T/W and T/F (HR 1.19 [0.84 − 1.69], p=0.34). Median RFS was 155 mo (95%CI 143-NR) with no significant difference between M/T/W and T/F (HR 1.22 [0.87 − 1.72], p=0.25). Median TTR was not reached, with no significant difference between M/T/W and T/F (HR 1.46 [0.96 − 2.22], p=0.07).
Conclusions
The day of the week of CT during CRT does not appear to impact recurrence or survival outcomes.
Clinical trial identification
Editorial acknowledgement
Funding
Has not received any funding.
Disclosure
R. Ferrarotto: Financial Interests, Personal, Advisory Board: Regeneron-Sanofi, Ayala Pharmaceuticals, Bicara Therapeutics, Prelude Therapeutics, Guidepoint, Elevar Therapeutics, G1 Therapeutics, ExpertConnect, Remix; Financial Interests, Personal, Invited Speaker: Merck; Financial Interests, Personal, Royalties: UptoDate; Financial Interests, Institutional, Coordinating PI: Merck, Gennentech, Pfizer, Ayala, EMD Serono; Financial Interests, Institutional, Other, Co-PI: Rakuten, Nanobiotix; Financial Interests, Institutional, Local PI: Prelude, ISA Therapeutics; Non-Financial Interests, Advisory Role: Cellestia. All other authors have declared no conflicts of interest.
Resources from the same session
792P - The differences in immunogenicity of TP53 mutated endometrial-, high-grade serous ovarian- and triple negative breast carcinomas
Presenter: Alain Zeimet
Session: Poster session 02
793TiP - A phase III, randomized, open-label, multicenter study of sacituzumab tirumotecan (sac-TMT) monotherapy vs treatment of physician’s choice chemotherapy in patients with endometrial cancer who have received prior chemotherapy and immunotherapy: ENGOT-en23/GOG-3095/MK-2870-005
Presenter: Domenica Lorusso
Session: Poster session 02
795TiP - A first-in-human phase I study of LY4170156, an antibody-drug conjugate targeting folate receptor α (FRα)-expressing advanced solid tumors
Presenter: Isabelle Ray-Coquard
Session: Poster session 02
796TiP - Rationale and study design of the KOV-HIPEC-04: A phase III randomized controlled trial in primary stage three and four ovarian cancer after interval cytoreductive surgery (FOCUS)
Presenter: Junhwan Kim
Session: Poster session 02
797TiP - Tislelizumab combined with chemotherapy as neoadjuvant treatment for advanced endometrial cancer: A prospective, single-arm, open-label clinical study
Presenter: Zheng Hu
Session: Poster session 02
798TiP - Stereotactic radiotherapy alone or followed by niraparib for oligometastases or oligoprogression in ovarian cancer following PARP inhibitor therapy: SOPRANO trial
Presenter: Susana Banerjee
Session: Poster session 02
856P - Safety of neoadjuvant PARP inhibitor and immunotherapy in locally advanced HPV-negative head and neck squamous cell carcinoma (PRIME H&N Study)
Presenter: Luigi Lorini
Session: Poster session 02
857P - Safety and efficacy of neoadjuvant immunochemotherapy in patients with locally advanced head and neck squamous cell carcinoma: A prospective single-arm clinical trial
Presenter: Jing Yan
Session: Poster session 02
Resources:
Abstract