Phase III randomized trial comparing palliative systemic therapy to best supportive care in advanced esophageal/GEJ cancer

Author:

Noronha Vanita1ORCID,Patil Vijay Maruti2,Menon Nandini1ORCID,Goud Supriya1,Singh Ajaykumar1,Shah Minit1,More Sucheta1,Shah Srushti1,Yadav Akanksha1,Sonawane Sonali1,Nawale Kavita1,Chowdhury Oindrila Roy1,Kaushal Rajiv Kumar3,Ghosh‐Laskar Sarbani4,Agarwal Jai Prakash4,Yadav Subhash3,Pai Trupti3,Janu Amit5,Mahajan Abhishek6,Purandare Nilendu7,Banavali Shripad1,Badwe Rajendra8,Prabhash Kumar1ORCID

Affiliation:

1. Department of Medical Oncology Tata Memorial Hospital, Homi Bhabha National Institute Mumbai India

2. Department of Medical Oncology P D Hinduja Hospital & Medical Research Centre Mumbai India

3. Department of Pathology Tata Memorial Hospital, Homi Bhabha National Institute Mumbai India

4. Department of Radiation Oncology Tata Memorial Hospital, Homi Bhabha National Institute Mumbai India

5. Department of Radiodiagnosis Tata Memorial Hospital, Homi Bhabha National Institute Mumbai India

6. The Clatterbridge Cancer Centre NHS Foundation Trust University of Liverpool Liverpool UK

7. Department of Nuclear Medicine Tata Memorial Hospital, Homi Bhabha National Institute Mumbai India

8. Department of Surgical Oncology Tata Memorial Hospital, Homi Bhabha National Institute Mumbai India

Abstract

AbstractNo study has unequivocally proven that chemotherapy prolongs overall survival (OS) in advanced esophageal cancer. We conducted a Phase III randomized study in first‐line advanced unresectable/metastatic esophageal/GEJ cancer. Patients aged 18–70 years, with performance status 0–2, were randomized to best supportive care (BSC) alone, or BSC with weekly paclitaxel 80 mg/m2. BSC comprised, as indicated, education, counselling, radiation, stenting, feeding tube placement, nutritional supplementation, medications like analgesics, and referral to a support group and palliative care. The primary endpoint was OS; secondary endpoints included progression free survival (PFS), response, toxicity, and QoL. Between May 2016–December 2020, we recruited 281 patients: 143 to chemotherapy and 138 to BSC. Histopathology was squamous in 269 (95.7%) patients. Median number of paclitaxel doses was 12 (IQR, 7–23). Median OS was 4.2 months (95% CI, 3.42–5.32) in BSC, and 9.2 months (95% CI, 8.02–10.48) in chemotherapy; HR, 0.49 (95% CI, 0.39–0.64); p < .001. As compared to BSC, chemotherapy increased response (2.9% to 39%), median PFS (2.1 to 4.2 months), 1‐year OS (11% to 32%), 2‐year OS (0 to 9%), median dysphagia‐free survival (2.9 to 14.8 months), and global and esophagus‐specific QoL, without significantly increasing all‐grade or grade ≥3 toxicities. Using ESMO clinical benefit scale and ASCO Value Framework, palliative chemotherapy scored as having “substantial value.” Our study provides the first level 1 evidence that chemotherapy prolongs survival in advanced esophageal/GEJ carcinoma. BSC alone is no longer appropriate. Weekly paclitaxel is an attractive option, especially in LMICs with limited access to immunotherapy.

Publisher

Wiley

Reference41 articles.

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