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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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1060965 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 Type1 V( i# l0 ]5 c( X. l- t
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
$ C* g5 e" t; D/ u9 x' z+ Author Affiliations( @7 i2 Y4 Z5 x  ^1 C% j$ ~$ }
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
0 Q8 b0 m7 B* ^! E0 {$ \" F, W* q2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
& h. N" n1 y( u3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
+ j( }6 f& H' d* g4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan , [8 F7 i! A; S1 e4 w  d
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
5 r# I' m2 ?0 E" t6 N0 k- g5 w! h6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 7 L6 w+ B4 b% Y. W- g! c  h
7Kinki University School of Medicine, Osaka 589-8511, Japan 9 G' P. x9 D" J! v4 e9 l7 }
8Izumi Municipal Hospital, Osaka 594-0071, Japan 3 x* x% i( _- M) Z) ~, q! c& D( v
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
3 I% S, W+ P, w2 lCorrespondence 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
7 L% O1 V* s  h- u; A7 h/ ?( EAbstractBackground: 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
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 2 i6 m7 z5 `/ c- ^

/ f/ B4 z* p  QAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  ! D& A% b% t& a  u, z
, ^8 e0 C6 s* \, g
Published online on: Thursday, December 1, 2011
1 S9 K! x& c$ _8 c- G6 N& {* H, l/ F1 w! F2 W
Doi: 10.3892/ol.2011.507
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Pages: 405-410 , n1 S+ {/ g$ X# _( T

7 m0 |- C* y% hAbstract:; m/ g: N& `6 Y$ b5 g
S-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 population
1 ^% y& \" b+ ]1 g5 L+ VF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
% o- }0 J3 Z$ `# R8 T8 D5 d+ Author Affiliations
0 o3 _3 D, Z( u1 @& q' L: G* p1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
4 D  W0 j) \: H' Z2Department of Thoracic Surgery, Kyoto University, Kyoto / B  g+ `) W; w" y  @0 T
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
1 X/ A  {/ \" H3 z) k6 ~6 y3 R&#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
7 _6 i+ Y( L& S& L8 q/ B. o5 H- p* pReceived September 3, 2010. $ K9 i* [2 c& J* q
Revision received November 11, 2010. " v8 f% x7 w! W  B3 e) v5 e7 @/ R* f2 V
Accepted November 17, 2010. ( v! t7 F) ]" p4 G% f
Abstract
: k% X, A5 U6 Z9 DBackground: 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.
0 [2 \" A3 W8 Z; l2 Y& `Patients 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. ) P; n  V1 \0 X) l+ D
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. 2 m' F3 n3 ^; w9 ~) D* ]* t
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. % T( @+ `9 d1 L& l9 ~8 z
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。
, l4 Y% L3 @' `& C* u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?
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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 Chemotherapy, w4 Y+ Y2 [. P
http://clinicaltrials.gov/ct2/show/NCT01523587# `. u0 Q1 v2 f, W

# s, B4 G- G, e9 X: BBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
2 G  I) f) m/ C: I% J1 ehttp://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 5 `, x7 J9 Y! j. r9 \* r

: U2 f' h) S8 X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。; g9 j/ X( i" u( R2 w( ^
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 ) v9 l3 `6 R( M& [$ S2 K
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。
! \+ j2 T* h5 x) i3 b. P9 w至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。1 i6 I: m( w+ W
不错。

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