Abstract 565P
Background
In early-stage rectal cancer, short term results of neoadjuvant chemotherapy combined with transanal endoscopic surgery (TES) demonstrate promise as a strategy for organ preservation with acceptable early oncologic and functional outcomes. The objective of this study was to analyse medium term oncologic and functional outcomes of the NEO trial patient cohort.
Methods
This multicenter, phase II trial included patients with clinical T1-T3abN0M0 low- or mid-rectal adenocarcinoma eligible for TES who were treated with 3 months of chemotherapy (mFOLFOX6 or CAPOX). Patients with endoscopic and MRI evidence of tumor response proceeded to TES within 6 weeks of treatment completion. All patients followed an intensive surveillance regimen for a minimum of 3 years postop, including endoscopy, MRI, CT scan and quality of life/ low anterior resection syndrome (LARS) questionnaires.
Results
Between August 2017 and May 2020, 58 patients were recruited at 7 North American centers. Of these, 71% (41/58) were male and median age was 66 (range 31-83) years. All patients commenced chemotherapy and 56 proceeded to TES. Of these, 33/58 (57%) patients had tumor downstaging to ypT0/1 and were recommended protocol-specified surveillance for organ preservation. While 10/23 patients with persistent yT2 agreed to total mesorectal excision (TME), 13 patients declined, resulting in 46/58 (79%) organ preservation. At median follow up 4.3 years (range 3.3 – 5.6 years), 4 patients experienced local recurrence: 3 endoluminal and 1 nodal. Overall, 3-year locoregional relapse free survival was 92.9% (95% CI 82.3-97.3%) and 3 year distant disease free survival was 94.7% (95%CI 84.6-98.3%). Overall disease free survival was 84.3% (95% CI 72.0-91.5[LJ[1] %). At 3 years post TES, major, minor, and no LARS was experienced in 22%, 19%, and 59%, respectively, in patients with successful organ preservation.
Conclusions
For patients with early rectal cancer, a novel strategy of three months of induction chemotherapy combined with TES achieved organ preservation with good oncologic and functional outcomes after 3 years of follow up in this phase II study.
Clinical trial identification
NCT03259035.
Editorial acknowledgement
Legal entity responsible for the study
Canadian Cancer Trials Group.
Funding
Canadian Cancer Trials Group (CCTG).
Disclosure
C.J. Brown: Financial Interests, Personal, Invited Speaker, Fellowship educational event: Ethicon; Financial Interests, Institutional, Funding, ebrs.online support: Medtronci. J.M. Loree: Financial Interests, Personal, Speaker, Consultant, Advisor: Amgen, Novartis, Ipsen, Bayer, Roche, Pfizer, Guardiant Health, Saga Diagnostics. R. Auer: Financial Interests, Personal, Speaker, Consultant, Advisor: Incyte; Financial Interests, Personal, Advisory Board: Takeda, Boehringer Ingelheim; Financial Interests, Personal, Speaker’s Bureau: Servier; Financial Interests, Institutional, Research Funding: Qu Biologics, Miso-chip. D. Jonker: Financial Interests, Institutional, Research Funding: Amgen, Pfizer, Genentech, 23me, GSK, AstraZeneca, Seagen, Janssen, Ocellaris, Signalchem, Arcus Biologics, Gilead, Qu Biologics. M. Raval: Financial Interests, Institutional, Research Funding: Cook Medical. V. Simianu: Financial Interests, Personal, Advisory Board: BD Surgical; Financial Interests, Personal, Advisory Role: C-SATS Inc; Financial Interests, Personal, Funding: Intuitive Surgical Inc. L. Pitre: Financial Interests, Personal, Speaker, Consultant, Advisor: Novartis, Merck, AstraZeneca; Financial Interests, Institutional, Funding: Pfizer. K. Neumann: Financial Interests, Institutional, Research Funding: GSK. D. Bosse: Financial Interests, Personal, Speaker’s Bureau: Ipsen, EMD Serono, Janssen; Financial Interests, Personal, Stocks/Shares: NEED; Financial Interests, Personal, Advisory Role: AstraZeneca, Bayer; Financial Interests, Personal, Speaker, Consultant, Advisor: Knight Pharmaceutical, Amgen, Merck, Abbvie, Pfizer, BMS, CUS. All other authors have declared no conflicts of interest.
Resources from the same session
567P - Interim endoscopic restaging after induction chemotherapy to predict complete response and survival after total neoadjuvant therapy in low rectal cancer: Ad-hoc analysis of the IMPACT trial
Presenter: Eiji Shinozaki
Session: Poster session 16
568P - Risk factors for recurrence after surgery for rectal cancer in a modern, nationwide population-based cohort
Presenter: Sepehr Doroudian
Session: Poster session 16
569P - Mismatch repair deficient, stage II/III rectal cancer: Real-world patient, tumour, and treatment characteristics in the Netherlands
Presenter: Renee Lunenberg
Session: Poster session 16
571P - Neoadjuvant chemotherapy with FOLFIRINOX and short course radiotherapy in locally advanced rectal caner (ISANOX): A prospective phase II trial
Presenter: Feryel Letaief-Ksontini
Session: Poster session 16
572P - Tolerance of adjuvant chemotherapy in older patients after resection of stage III colon adenocarcinoma from PRODIGE 34 – FFCD 1402 - ADAGE randomized phase III trial
Presenter: Thomas Aparicio
Session: Poster session 16
573P - M9140, an anti-CEACAM5 antibody drug conjugate (ADC), in patients with metastatic colorectal cancer (mCRC): Updated results from a phase I trial
Presenter: Valentina Boni
Session: Poster session 16
574P - First-in-class PD-1/IL-2 bispecific antibody fusion protein IBI363 + bevacizumab (beva) in patients (pts) with advanced colorectal cancer (CRC): A phase I study
Presenter: Zhen Yu Lin
Session: Poster session 16
575P - Phase Ib/II study of ompenaclid (RGX-202-01), a first-in-class oral inhibitor of the creatine transporter SLC6A8, in combination with FOLFIRI and bevacizumab (BEV) in RAS mutated (RASmt) second-line (2L) advanced/metastatic colorectal cancer (mCRC): Updated results
Presenter: Andrew Hendifar
Session: Poster session 16
576P - Safety and efficacy of IBI354 (anti-HER2 ADC) in patients (pts) with advanced gastrointestinal (GI) cancers: Results from a phase I study
Presenter: Jifang Gong
Session: Poster session 16