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Home » Cancer Management Handbook, 11th Edition » Chapter 1: Principles of Surgical Oncology

Cancer Management: A Multidisciplinary Approach, 11th Edition (2008).
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Chapter 1 

Principles of Surgical Oncology

By Lawrence D. Wagman, MD | April 8, 2009

Surgical oncology, as its name suggests, is the specific application of surgical principles to the oncologic setting. These principles have been derived by adapting standard surgical approaches to the unique situations that arise when treating cancer patients.

The surgeon is often the first specialist to see the patient with a solid malignancy, and, in the course of therapy, he or she may be called upon to provide diagnostic, therapeutic, palliative, and supportive care. In each of these areas, guiding paradigms that are unique to surgical oncology are employed.

In addition, the surgical oncologist must be knowledgeable about all of the available surgical and adjuvant therapies, both standard and experimental, for a particular cancer. This enables the surgeon not only to explain the various treatment options to the patient but also to perform the initial steps in diagnosis and treatment in such a way as to facilitate and avoid interfering with future therapeutic options.

Invasive diagnostic modalities

As the surgeon approaches the patient with a solid malignancy or abnormal nodal disease or the rare individual with a tissue-based manifestation of a leukemia, selection of a diagnostic approach that will have a high likelihood of a specific, accurate diagnosis is paramount. The advent of high-quality invasive diagnostic approaches guided by radiologic imaging modalities has limited the open surgical approach to those situations where the disease is inaccessible, a significant amount of tissue is required for diagnosis, or a percutaneous approach is too dangerous (due, for example, to a bleeding diathesis, critical intervening structures, or the potential for unacceptable complications, such as pneumothorax).

Lymph node biopsy

The usual indication for biopsy of the lymph node is to establish the diagnosis of lymphoma or metastatic carcinoma. Each situation should be approached in a different manner.

Lymphoma The goal of biopsy in the patient with an abnormal lymph node and suspected lymphoma is to make the general diagnosis and to establish the lymphoma type and subtype. Additional analyses of the cells in the node, its internal architecture, and the subpopulations of cells are critical for subsequent treatment. Although advances in immunocytochemical and histochemical analyses have been made, adequate tissue is the key element in accurate diagnosis.

Consequently, the initial diagnosis of lymphoma should be made on a completely excised node that has been minimally manipulated to ensure that there is little crush damage. When primary lymphoma is suspected, the use of needle aspiration does not consistently allow for the complete analyses described above and can lead to incomplete or inaccurate diagnosis and treatment delays.

When recurrent lymphoma is the primary diagnosis, analysis of a specific cell type is important for assessing changes in the type of lymphoma and whether a transformation has occurred. In the rare situation in which recurrent Hodgkin lymphoma is suspected, a core biopsy may be adequate if the classic Reed-Sternberg cells are identified. However, in the initial and recurrent settings, biopsy of an intact node is often required.

Carcinoma The diagnosis of metastatic carcinoma often requires less tissue than is needed for lymphoma. Fine-needle aspiration (FNA), core biopsy, or subtotal removal of a single node will be adequate in this situation. For metastatic disease, the surgeon will use a combination of factors, such as location of the node, physical examination, and symptoms, to predict the site of primary disease. When this information is communicated to the pathologist, the pathologic evaluation can be focused on the most likely sites so as to obtain the highest diagnostic yield. The use of immunocytochemical analyses can be successful in defining the primary site, even on small amounts of tissue.

Head and neck adenopathy The head and neck region is a common site of palpable adenopathy that poses a significant diagnostic dilemma. Nodal zones in this area serve as the harbinger of lymphoma (particularly Hodgkin lymphoma) and as sites of metastasis from the mucosal surfaces of the upper aerodigestive tract; nasopharynx; thyroid; lungs; and, occasionally, intra-abdominal sites, such as the stomach, liver, and pancreas.

Because treatment of these nodal metastases varies widely, and subsequent treatments may be jeopardized by inconveniently placed biopsy incisions, the surgical oncologist must consider the most likely source of the disease prior to performing the biopsy. FNA or core biopsy becomes a valuable tool in this situation, as the tissue sample is usually adequate for basic analysis (cytologic or histologic), and special studies (eg, immunocytochemical analyses) can be performed as needed.

Biopsy of a tissue-based mass

Several principles must be considered when approaching the seemingly simple task of biopsying a tissue-based mass. As each of the biopsy methods has unique risks, yields, and costs, the initial choice can be a critical factor in the timeliness and expense of the diagnostic process. It is crucial that the physician charged with making the invasive diagnosis be mindful of these factors.

Mass in the aerodigestive tract In the aerodigestive tract, biopsy of a lesion should include a representative amount of tissue taken preferably from the periphery of the lesion, where the maximum amount of viable malignant cells will be present. Because the treatment of in situ and invasive diseases varies greatly, the biopsy must be of adequate depth to determine penetration of the tumors. This is particularly true for carcinomas of the oral cavity, pharynx, and larynx.

Breast mass Although previously a common procedure, an open surgical biopsy of the breast is rarely indicated today. Palpable breast masses that are highly suspicious (as indicated by physical findings and mammography) can be diagnosed as malignant with close to 100% accuracy with FNA. However, because the distinction between invasive and noninvasive diseases is often required prior to the initiation of treatment, a core biopsy, performed either under image guidance (ultrasonography or mammography) or directly for palpable lesions, is the method of choice.

An excellent example of the interdependence of the method of tissue diagnosis and therapeutic options is the patient with a moderate-sized breast tumor considering breast conservation who chooses preoperative chemotherapy for downsizing of the breast lesion. The core biopsy method establishes the histologic diagnosis, provides adequate tissue for analyses of hormone-receptor levels and other risk factors, causes little or no cosmetic damage, does not perturb sentinel node analyses, and does not require extended healing prior to the initiation of therapy. In addition, a small radioopaque clip can be placed in the tumor to guide the surgical extirpation. This step is important because excellent treatment responses can make it difficult for the surgeon to localize the original tumor site.

Mass in the trunk or extremities For soft-tissue or bony masses of the trunk or extremities, the biopsy technique should be selected on the basis of the planned subsequent tumor resection. The incision should be made along anatomic lines in the trunk or along the long axis of the extremity. When a sarcoma is suspected, FNA can establish the diagnosis of malignancy, but a core biopsy will likely be required to determine the histologic type and plan neoadjuvant therapy.

Preoperative evaluation

As with any surgical patient, the preoperative evaluation of the cancer patient hinges primarily on the individual's underlying medical condition(s). Because most new cancers occur in older patients, careful attention must be paid to evaluation of cardiovascular risks. Adequate information can usually be obtained from a standard history, physical examination, and electrocardiogram (ECG), but any concerns identified should be subjected to a full diagnostic work-up.

The evaluation should also include a detailed history of current and previous therapies. Many patients will be on anticoagulation, aspirin, or analgesics, all of which may impact on their perioperative management. Previous use of doxorubicin or trastuzumab (Herceptin) may be associated with cardiac dysfunction and the use of bleomycin with severe lung sensitivity to oxygen concentrations > 30%. Due to the association of bowel anastomotic perforation with the use of bevacizumab (Avastin), the timing of colonic surgery should be modified. Some of the cytotoxic agents (oxaliplatin [Eloxatin], irinotecan) used to treat colon and rectal cancers are associated with liver injury.

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Table of Contents

14TH EDITION ONLINE ONLY

Cancer Management: A Multidisciplinary Approach

Medical, Surgical, & Radiation Oncology

 

Edited by
Daniel G. Haller, MD
Professor of Medicine Emeritus
Abramson Cancer Center at the University of Pennsylvania
 

Lawrence D. Wagman, MD
Executive Medical Director
The Center for Cancer Prevention and Treatment
St. Joseph Hospital
 

Kevin A. Camphausen, MD
Chief, Radiation Oncologist, National Cancer Institute

William J. Hoskins, MD
Executive Director of Surgical Activities
Memorial Sloan-Kettering Cancer Center
 

And the publishers of the journal ONCOLOGY

   

 


  

cancers of the head and neck region

Ch 1 Head and Neck Tumors
John Andrew Ridge, Bonnie S. Glisson, Miriam N. Lango, Steven Feigenberg

Ch 2 Thyroid and Parathyroid Cancers 
Erika Masuda Alford, Mimi I. Hu, Peter Ahn, Jeffrey P. Lamont

 

LUNG CANCER

Ch 3 Non-Small-Cell Lung Cancer
Benjamin Movsas, Julie Brahmer, Channing Paller, Kemp H. Kernstine

Ch 4 Small-Cell Lung Cancer, Mesothelioma, and Thymoma
Bonnie S. Glisson, Benjamin Movsas, Walter Scott, Robert A. Chapman

 

Breast cancer

Ch 5 Breast Cancer Overview Risk factors, screening, genetic testing, and prevention
Lori Jardines, Sharad Goyal, Paul Fisher, Jeffrey Weitzel, Melanie Royce, Shari B. Goldfarb

Ch 6 Stages 0 and I Breast Cancer
Lori Jardines, Sharad Goyal, Melanie Royce, Shari B. Goldfarb

Ch 7 Stage II Breast Cancer
Lori Jardines, Sharad Goyal, Melanie Royce, Shari B. Goldfarb

Ch 8 Stages III and IV Breast Cancer
Lori Jardines, Sharad Goyal, Melanie Royce, Ishmael Jaiyesimi, Shari B. Goldfarb

 

GASTROINTESTINAL CANCERS

Ch 9 Esophageal Cancer
Jimmy J. Hwang, Rajesh V. Iyer, Michael Mulligan

Ch 10 Gastric Cancer
Charles D. Blanke, Deborah Citrin, Roderich E. Schwarz

Ch 11 Pancreatic, Neuroendocrine GI, and Adrenal Cancers
Al B. Benson III, Robert J. Myerson, Aaron Sasson

Ch 12 Liver, Gallbladder, and Biliary Tract Cancers
Lawrence D. Wagman, John M. Robertson, Laura Raftery, Bert O'Neil, Keeran R. Sampat

Ch 13 Colon, Rectal, and Anal Cancers
Steven R. Alberts, Deborah Citrin, Miguel Rodriguez-Bigas

 

GENITOURINARY MALIGNANCIES

Ch 14 Prostate Cancer
Judd W. Moul, Andrew J. Armstrong, Joseph Lattanzi

Ch 15 Testicular Cancer
Patrick J. Loehrer, Atreya Dash, Mark K. Buyyounouski, Douglas Skarecky, Tareq Al Baghdadi

Ch 16 Urothelial and Kidney Cancers
Mark Hurwitz, Philippe E. Spiess, Jorge A. Garcia, Louis L. Pisters

 

GYNECOLOGIC MALIGNANCIES

Ch 17 Cervical Cancer
Leda Gattoc, Carlos A. Perez, William Tew, Sharmila Makhija

Ch 18 Uterine Corpus Tumors
Kathryn M. Greven, Maurie Markman, David Scott Miller

Ch 19 Ovarian Cancer
Stephen C. Rubin, Paul Sabbatini, Akila N. Viswanathan

 

SKIN CANCERS

Ch 20 Melanoma and Other Skin Cancers
Mary S. Brady, Aradhana Kaushal, Christine Ko, Keith Flaherty

 

Sarcomas

Ch 21 Bone Sarcomas
Warren Chow, Karl Haglund, R. Lor Randall

Ch 22 Soft-Tissue Sarcomas
Peter W. T. Pisters, Mitchell Weiss, Robert Maki

 

Brain TUMORS

Ch 23 Primary and Metastatic Brain Tumors
Jay S. Loeffler, John de Groot, Nicole Shonka, Daniel P. Cahill

 

other SOLID TUMORS

Ch 24 AIDS-Related Malignancies
Ronald T. Mitsuyasu, Deepa Reddy, Jay S. Cooper

Ch 25 Carcinoma of an Unknown Primary Site
John D. Hainsworth, Lawrence M. Weiss

 

hematologic malignancies

Ch 26 Hodgkin Lymphoma
Joachim Yahalom, David Straus, Dennis Eichenauer, Volker Diehl

Ch 27 Non-Hodgkin Lymphoma
Andrew M. Evens, Jane N. Winter, Leo I. Gordon, Brian C.-H. Chiu, Richard Tsang, Steven T. Rosen

Ch 28 Multiple Myeloma and Other Plasma Cell Dyscrasias
Sundar Jagannath, Paul Richardson, Nikhil C. Munshi

Ch 29 Acute Leukemias
Margaret R. O'Donnell

Ch 30 Chronic Myeloid Leukemia
Jorge E. Cortes, Richard T. Silver, Hagop Kantarjian

Ch 31 Chronic Lymphocytic Leukemia
Nicole Lamanna, Mark A. Weiss, Kieron Dunleavy

Ch 32 Myelodysplastic Syndromes
Guillermo Garcia-Manero, Alan List, Hagop Kantarjian, Jorge E. Cortes

Ch 33 Hematopoietic Cell Transplantation
Stephen J. Forman, Ryotaro Nakamura

 

Palliative and SUPPORTIVE CARE

Ch 34 Pain Management
Sharon M. Weinstein, Nora Janjan

Ch 35 Management of Nausea and Vomiting
Steven M. Grunberg, Nathan B. Adams, Richard Gralla

Ch 36 Fatigue and Dyspnea
Sriram Yennurajalingam, Eduardo Bruera

Ch 37 Anorexia and Cachexia
Aminah Jatoi

 

COMPLICATIONS

Ch 38 Oncologic Emergencies and Paraneoplastic Syndromes
Carmen P. Escalante, Ellen Manzullo, Mitchell Weiss

Ch 39 Infectious Complications
Sanjeet Dadwal, Jane Kriengkauykiat, James Ito

Ch 40 Fluid Complications
Frederic W. Grannis, Jr., Lily Lai

Ch 41 Long-Term Central Venous Access
Stephen P. Povoski
 

Color Atlases

Color Atlas 1: The ABCDEs of Moles and Melanomas

Color Atlas 2: Skin Lesions

Color Atlas 3: Dermatologic Toxicities Associated With Targeted Therapies
 

APPENDICES

Appendix 1: Response Evaluation Criteria and Performance Scales

Appendix 2: Cancer Information on the Internet
J. Sybil Biermann

Appendix 3: Cancer Drugs and Indications Newly Approved by the US Food and Drug Administration

Appendix 4: Chemotherapeutic Agents and Their Uses, Dosages, and Toxicities

Emiliano Calvo, MD, PhD and Antonio Calles, MD

 




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