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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1111696 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
/ a2 [' V# Y4 m! S7 A3 WNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 % n8 @$ S& o, ]- l9 P& d  G
+ Author Affiliations& j/ _# a' ]- X/ i1 C

# n3 @& c4 h; r5 Y% x1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan " z& j7 I8 u7 z: S) S- l
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan - U/ c6 F( R- ?4 b, T% S
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
8 d& ~1 t$ I  c# Q' @% z8 e6 F4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
& |9 `; ~/ G4 B% C7 ?; H8 Q! G5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ( g( q! C* S: b% b/ H9 F1 S% y
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
  L8 t2 b6 O4 g2 y. d' c0 W+ v7Kinki University School of Medicine, Osaka 589-8511, Japan
) x0 L- F' A, H* H) O. J' c* _8Izumi Municipal Hospital, Osaka 594-0071, Japan
1 A( [7 ?3 s. U% L: z9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
( A8 z+ M8 |0 F( V9 M+ RCorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
9 ]7 X2 o! X0 S% U8 B  aAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type $ F  z3 H: t) n

) ~0 W: Z; L2 ]: f$ t7 s. B  u( XAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
* k+ x0 M! L) _. Q0 Q" V! ~1 h1 s& z0 Q
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
1 i% S% g& G9 Y$ {' e2 ?4 v/ Q
6 I2 {3 d6 s1 Y2 r) `, V# \, E6 _: uPublished online on: Thursday, December 1, 2011
  J3 Y6 T1 s! J( c. L+ I4 l/ y0 u3 f% t( Q0 t1 @( X4 @) t9 l( y
Doi: 10.3892/ol.2011.507
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Pages: 405-410
5 `: [6 P0 B' m8 y0 M. ~( N: [" M2 G0 K! {- M
Abstract:
8 H  l' f; }0 eS-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population4 ^& n6 t9 g0 _9 ^! w
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 7 P8 n) S7 X, m6 K
+ Author Affiliations
) a1 U' \* n! X; `1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 1 @) F+ I6 O0 f; p
2Department of Thoracic Surgery, Kyoto University, Kyoto   t* l$ `  R. v, t2 |* d$ p
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan " {) K! z8 n) H" T9 a  o
&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp / r# K7 f5 V. P: p
Received September 3, 2010. - m( W4 H! H2 ~' p8 u+ a
Revision received November 11, 2010. ( }- O4 |0 ~, j2 E3 F' K4 u
Accepted November 17, 2010. / y' m$ _' \2 ^2 J( ~4 O" L
Abstract: @& f- _% Z& M2 {/ o7 J
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed.
" E+ f. g/ @  @# OPatients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. + Y8 v3 ]- J! p4 ]7 Q
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression. : p/ O2 Q, v* u& X/ g- B  g+ v
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 5 w1 q! x0 b, J; ?& X( m
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。; F, ?; B' e5 C# }' S
今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?; Q" H' M6 E0 ^4 Y, ^1 c4 G: [7 j
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy5 ^0 T# i: d& n+ c( E% e5 w
http://clinicaltrials.gov/ct2/show/NCT01523587( L* I4 I  z. Z5 q0 _
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC* D9 f/ S. O2 B- s9 T" B
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑
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! x4 T$ H( t/ X6 p* c/ N从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。5 z4 O) d# G) }# q
至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53
  C* N  ?( a, t1 D从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。6 C* T# X! l( p- o# t* Z! p. k
至今为止,未出 ...
+ s1 k) D# a2 v! W" N0 ]
没有副作用是第一追求,效果显著是第二追求。
: |) v; @' r4 [9 l不错。

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