Abstract 1584P
Background
The impact of TB (which contributes to both financial and time toxicities) on cancer treatment and outcomes, especially in RLS remains largely understudied. We assessed the impact of TB on the outcomes of patients with CRC treated at a regional cancer center in RLS.
Methods
All patients with newly diagnosed CRC in 2022 at the State Cancer Institute, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, North India were enrolled. TB was recorded as the average time required to traverse the shortest distance between the cancer center and the place of the patient’s residence.
Results
263 patients (42.6% females) with CRC were included, including patients who travelled from their homes (group A) and those who rented apartments near the hospital to complete treatment (group B). Group A patients (N=178) travelled 22 km (48 mins) [median] to reach the cancer center while Group B patients (N=85) resided 75 km (130 mins) [median] away from the hospital. Travel time did not correlate with symptom duration prior to diagnosis of CRC. In group A, patients with highest TB (Q4 travel time) had poorer outcomes than other patients (Q1-Q3 of travel time) (18-month OS of 65% v 83.6%, adjusted HR 2.5 [95% CI 1.2 to 5.2]) (Table). 18-month OS in group B was higher than that for group A patients (85.6% v 78.9%, p=0.056). Table: 1584P
Predictors of OS in patients with CRC [data expressed as HR (95% CI), p-value]
Parameter | Group A | Group B | ||
Univariate analysis | Multivariate analysis | Univariate analysis | Multivariate analysis | |
1. Age ≥50 years | 1.6 (0.8 to 3.5), 0.2 | 1.3 (0.3 to 6.4), 0.8 | ||
2. Female sex | 0.8 (0.4 to 1.5), 0.4 | 0.5 (0.1 to 2.3), 0.3 | ||
3. Presence of comorbidity | 1.1 (0.5 to 2.1), 0.8 | 0.0 (0.0 to 8.0), 0.2 | ||
4. ECOG >1 | 3.6 (1.7 to 7.5), 0.001 | 3.4 (1.4 to 7.9), 0.005 | 0.8 (0.1 to 6.7), 0.9 | |
5. Left vs right colon | 1.3 (0.5 to 3.5), 0.6 | 1.6 (0.12 to 13.4), 0.7 | ||
6. Metastatic disease | 8.1 (4.0 to 16.2), ConclusionsOur study demonstrates that TB is significantly associated with poorer outcomes in patients with CRC. Clinical trial identificationEditorial acknowledgementLegal entity responsible for the studyS.Z. Banday. FundingHas not received any funding. DisclosureB. Gyawali: Financial Interests, Personal, Writing Engagement, For writing Medscape Columns: Medscape; Financial Interests, Personal, Invited Speaker, For giving invited talks and grand rounds at universities, cancer centers and professional societies: Various academic and professional organizations; Financial Interests, Personal, Other, Consulting services: Vivio Health; Non-Financial Interests, Member: ASCO, IASLC, JSMO. All other authors have declared no conflicts of interest. Resources from the same session1607P - Association of the lipid biomarker, PCPro, and clinical outcomes in the ENZAMET trial (ANZUP 1304)Presenter: Lisa Horvath Session: Poster session 10 1608P - Prostate cancer working group 4 (PCWG4) preliminary criteria using serial PSMA PET/CT for response evaluation: Analysis from the PRINCE trialPresenter: Michael Hofman Session: Poster session 10 1609P - PSMA-PET and PROMISE re-define stage and risk in patients with prostate cancerPresenter: Wolfgang Fendler Session: Poster session 10 1610P - Circulating tumour cell (CTC) enumeration and overall survival (OS) in men with metastatic castration-resistant prostate cancer (mCRPC) treated with xaluritamigPresenter: Andrew Armstrong Session: Poster session 10 1611P - Haematologic impact of [177Lu]Lu-PSMA-617 versus ARPI change in patients with metastatic castration-resistant prostate cancer in PSMAforePresenter: Kim Nguyen Chi Session: Poster session 10 1612P - Impact of FANCA, ATM, CDK12 alterations on survival in metastatic castration-resistant prostate cancer (mCRPC)Presenter: David Lorente Session: Poster session 10 1613P - Clinically advanced prostate cancer (CAPC) featuring BRCA2 loss: A comprehensive genomic profiling (CGP) studyPresenter: Chiara Mercinelli Session: Poster session 10 1614P - PSA responses and PSMA scan changes after immunotherapy for biochemically recurrent prostate cancer (BCR) without androgen deprivation therapy (ADT)Presenter: Ravi Madan Session: Poster session 10 1615P - A new prognostic model of overall survival (OS) in patients (pts) with metastatic hormone sensitive prostate cancer (mHSPC)Presenter: Susan Halabi Session: Poster session 10 This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used. For more detailed information on the cookies we use, please check our Privacy Policy.
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