Radiographic and Serologic Response to First-Line Chemotherapy in Unresected Localized Pancreatic Cancer

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Caitlin A. Hester Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas;

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Giampaolo Perri Department of General and Pancreatic Surgery, University of Verona, Verona, Italy; and

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Laura R. Prakash Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas;

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Jessica E. Maxwell Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas;

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Naruhiko Ikoma Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas;

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Michael P. Kim Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas;

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Ching-Wei D. Tzeng Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas;

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Brandon Smaglo Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

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Robert Wolff Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

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Milind Javle Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

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Michael J. Overman Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

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Jeffrey E. Lee Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas;

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Matthew H.G. Katz Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas;

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Background: This study aimed to determine the clinical relevance of putative radiographic and serologic metrics of chemotherapy response in patients with localized pancreatic cancer (LPC) who do not undergo pancreatectomy. Studies evaluating the response of LPC to systemic chemotherapy have focused on histopathologic analyses of resected specimens, but such specimens are not available for patients who do not undergo resection. We previously showed that changes in tumor volume and CA 19-9 levels provide a clinical readout of histopathologic response to preoperative therapy. Methods: Our institutional database was searched for patients with LPC who were treated with first-line chemotherapy between January 2010 and December 2017 and did not undergo pancreatectomy. Radiographic response was measured using RECIST 1.1 and tumor volume. The volume of the primary tumor was compared between pretreatment and posttreatment images. The percentage change in tumor volume (%Δvol) was calculated as a percentage of the pretreatment volume. Serologic response was measured by comparing pretreatment and posttreatment CA 19-9 levels. We established 3 response groups by combining these metrics: (1) best responders with a decline in %Δvol in the top quartile and in CA 19-9, (2) nonresponders with an increase in %Δvol and in CA 19-9, and (3) other patients. Results: This study included 329 patients. Individually, %Δvol and change in CA 19-9 were associated with overall survival (OS) (P≤.1), but RECIST 1.1 was not. In all, 73 patients (22%) were best responders, 42 (13%) were nonresponders, and there were 214 (65%) others. Best responders lived significantly longer than nonresponders and others (median OS, 24 vs 12 vs 17 months, respectively; P<.01). A multivariable model adjusting for type of chemotherapy regimen, number of chemotherapy doses, and receipt of radiotherapy showed that best responders had longer OS than did the other cohorts (hazard ratio [HR], 0.35; 95% CI, 0.21–0.58 for best responders, and HR, 0.55; 95% CI, 0.37–0.83 for others). Conclusions: Changes in tumor volume and serum levels of CA 19-9—but not RECIST 1.1—represent reliable metrics of response to systemic chemotherapy. They can be used to counsel patients and families on survival expectations even if pancreatectomy is not performed.

Submitted September 20, 2021; final revision received March 1, 2022; accepted for publication April 14, 2022.

Disclosures: Dr. Javle has disclosed serving on the data safety monitoring board for Oncosil and Incyte; and has served as a scientific advisor for Bristol Myers Squibb, Merck, QED Therapeutics, Helsinn, EMD Serono, Incyte, Taiho, Servier, AstraZeneca, Genentech, Zymeworks, Transthera, Meclun, Bayer, Novartis, and Boehringer Ingelheim. Dr. Overman has disclosed receiving grant/research support from Roche, Takeda, Merck & Co., Bristol Myers Squibb, AstraZeneca, and Nouscom; and serving as a consultant for Phanes Therapeutics, Takeda Pharmaceuticals, Ipsen Biopharmaceuticals, Pfizer, Merck & Co., GlaxoSmithKline, Promega, 3D Medicine, Nouscom, Gritstone, Tempus, and Roche. The remaining authors have disclosed that they have not received any financial consideration from any person or organization to support the preparation, analysis, results, or discussion of this article.

Correspondence: Matthew H.G. Katz, MD, Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030. Email: mhgkatz@mdanderson.org

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